Compounds > transferrin
Page last updated: 2024-08-23

transferrin and Genetic Predisposition

transferrin has been researched along with Genetic Predisposition in 82 studies

Research

Studies (82)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (2.44)18.2507
2000's38 (46.34)29.6817
2010's35 (42.68)24.3611
2020's7 (8.54)2.80

Authors

AuthorsStudies
Baráth, P; Bellová, J; Brucknerová, I; Brucknerová, J; Bzdúch, V; Hlavatá, A; Hrčková, G; Lekka, DE; Mc Cullough, A; Mucha, J; Nemčovič, M; Ostrožlíková, M; Pakanová, Z; Šalingová, A; Šebová, C; Šesták, S; Siváková, B; Skokňová, M; Ziburová, J1
Ahmed, AA; Al-Shaer, OS; Behiry, EG; Moustafa, HH1
Larsson, S; Yuan, S1
Burgess, S; Carter, P; Giovannucci, E; Kar, S; Larsson, SC; Mason, AM; Vithayathil, M; Yuan, S1
Crane, PK; Gonzalez Murcia, JD; Kauwe, JSK; Miller, JB; Mukherjee, S; Staley, L; Vance, E1
Deng, X; Jiang, D; Wang, Y; Zhou, M1
Al-Amer, O; Alsharif, KF1
Del Greco M, F; Gill, D; Laffan, MA; Minelli, C; Srai, SKS; Walker, AP1
Benyamin, B; Byrne, EM; Byrne, GJ; Colodro-Conde, L; CouvyDuchesne, B; Hansell, NK; Henders, AK; Maier, R; Martin, NG; Mills, NT; Montgomery, GW; Scott, JG; Vinkhuyzen, AAE; Whitfield, JB; Wray, NR; Wright, MJ1
Hong, YC; Kim, KN; Lee, MR; Lim, YH1
Antón, AI; Ballesta-Martínez, MJ; Corral, J; de la Morena-Barrio, ME; Del Campo, M; García-Algar, O; Guillén-Navarro, E; López-Gálvez, R; López-González, V; Martínez-Ribot, L; Miñano, A; Padilla, J; Vicente, V1
Bergsland, N; Dwyer, MG; Hagemeier, J; Lin, F; Ramanathan, M; Schweser, F; Weinstock-Guttman, B; Zivadinov, R1
Brissot, P; Cançado, RD; Dinardo, CL; Fonseca, GHH; Fonseca, PFS; Gualandro, SFM; Krieger, JE; Naoum, FA; Pereira, AC; Santos, PCJL1
Asselta, R; Bosi, C; Franchini, E; Gemmati, D; Greco, A; Longo, G; Ortolani, B; Paraboschi, EM; Secchiero, P; Serino, ML; Seripa, D; Tisato, V; Vigliano, M; Vikram Singh, A; Zauli, G; Zuliani, G; Zurlo, A1
Asteggiano, CG; Azar, NB; Bistué Millón, MB; Dodelson de Kremer, R; Guelbert, N; Papazoglu, M; Peralta, MF; Pereyra, M; Spécola, NS; Suldrup, NS1
Covey, CJ; Crownover, BK1
Bakashi, R; Hegade, VS; Kelly, SM; Sood, R1
Andersen, HU; Birgens, H; Ellervik, C; Frandsen, M; Mandrup-Poulsen, T; Nordestgaard, BG; Tybjærg-Hansen, A1
Bi, JZ; Lai, C; Liu, Z; Wang, Y; Wei, Y; Xie, Z; Xu, S; Zhao, C1
Amin, N; Anderson, D; Bandinelli, S; Beilby, J; Benyamin, B; Broer, L; Camaschella, C; Demirkan, A; Esko, T; Franke, L; Gieger, C; Gögele, M; Häldin, J; Hälldin, J; Heath, AC; Hernandez, D; Hicks, AA; Hui, J; Isaacs, A; Jolley, J; Kiemeney, LA; Kutalik, Z; Langenberg, C; Luan, J; Madden, PA; Martin, NG; Meitinger, T; Metspalu, A; Mihailov, E; Milani, L; Montgomery, GW; Nyholt, DR; Oexle, K; Ouwehand, WH; Peters, A; Pichler, I; Podmore, C; Powell, JE; Pramstaller, PP; Radhakrishnan, A; Rendon, A; Ried, JS; Sala, CF; Sambrook, J; Sanna, S; Schwienbacher, C; Scott, RA; Steri, M; Sweep, FC; Swinkels, DW; Tanaka, T; Thiery, J; Toniolo, D; Traglia, M; Uda, M; van der Harst, P; van der Meer, P; van Duijn, C; Vermeulen, SH; Verweij, N; Visscher, PM; Vollenweider, P; Waeber, G; Waldenberger, M; Wang, F; Wareham, NJ; Westra, HJ; Whitfield, JB; Winkelmann, J; Wright, MJ1
Fitzsimons, EJ; Gaffney, D; Haig, C; Kerry, A; Murray, H; Ogilvie, C; Spooner, R1
Feskens, EJ; Gichohi-Wainaina, WN; Melse-Boonstra, A; Swinkels, DW; Towers, GW; Zimmermann, MB1
Francis, S; Thachil, J1
Chun, S; Jeong, TD; Lee, W; Min, WK; Oh, SH1
Santos, PC1
Acosta, D; Caldés, T; de la Hoya, M; de Las Heras, N; Díaz-Millán, I; Díaz-Rubio, E; Lahera, V; López Farré, A; Melander, O; Modrego, J; Perez-Segura, P; Rico Zalba, LA; Santos-Sancho, JM; Zamorano-León, JJ1
Burgdorf, KS; Erikstrup, C; Hjalgrim, H; Pedersen, OB; Petersen, MS; Rigas, AS; Sørensen, E; Thørner, LW; Ullum, H1
Camaschella, C1
Bromhead, C; O'Toole, R; Romeril, K1
Altindal, M; Altun, B; Aybal Kutlugun, A; Eldem, G; Hazirolan, T; Turkmen, E; Yildirim, T; Yilmaz, E; Yilmaz, R1
Al Teneiji, A; Bruun, TU; Cohn, RD; Cordeiro, D; Kyriakopoulou, L; Mendoza-Londono, R; Mercimek-Mahmutoglu, S; Moharir, M; Raiman, J; Sidky, S; Siriwardena, K1
Allen, KJ; Anderson, GJ; Bahlo, M; Beckman, KB; Bertalli, NA; Chen, V; Constantine, CC; Delatycki, MB; English, DR; Gertig, DM; Giles, GG; Gurrin, LC; Hopper, JL; Matak, P; McKie, AT; McLaren, CE; Olynyk, JK; Osborne, NJ; Southey, MC; Vulpe, CD; Yeap, HL1
Acton, RT; Adams, PC; Barton, JC; Eckfeldt, JH; Leiendecker-Foster, C; McLaren, GD; Pankow, JS; Speechley, M1
Ariyaratnam, R; Burke, MJ; Pande, SD1
Aranda, N; Arija, V; Montserrat, C; Viteri, FE1
Altés, A; Baiget, M; Barceló, MJ; Crespo, L; Félez, J; Freixenet, N; Moreno-Rosel, MS; Payà, M; Pérez-Lucena, MJ; Serrano, A1
Brice, SE; Fertleman, M; Wolf, M1
Bassett, ML1
Arriola, JA; Castiella, A; de Juan, MD; Fernandez, J; Otazua, P; Zapata, E; Zubiaurre, L1
Cox, TM; Davies, SE; Douds, A; Finkenstedt, A; Griffiths, WJ; Halsall, DJ; Hermann, M; Janecke, AR; Mayr, R; McFarlane, I; Vogel, W; Zoller, H1
Blasiak, J; Dorecka, M; Kolodziejska, U; Romaniuk, D; Sklodowska, A; Szaflik, J; Szaflik, JP; Wozniak, K; Wysokinski, D1
Bucossi, S; Cassetta, E; Dell'acqua, ML; Giambattistelli, F; Mariani, S; Panetta, V; Rossini, PM; Salustri, C; Siotto, M; Squitti, R; Ventriglia, M; Vernieri, F1
Buretić-Tomljanović, A; Jonovska, S; Kapović, M; Ristić, S; Rubeša, G; Sendula-Jengić, V; Tomljanović, D; Vraneković, J1
An, P; Guan, Y; Li, L; Liao, Y; Man, Q; Meng, L; Mu, M; Song, P; Wang, C; Wang, F; Wang, H; Wu, Q; Zhang, J; Zhou, D1
He, M; Hu, FB; Manson, JE; Qi, L; Workalemahu, T1
Bassett, ML; Murtagh, LJ; Tran, H; Whiley, M; Wilson, S1
Isogai, S; Ouchi, H1
Beutler, E1
Ajioka, RS; Kushner, JP1
Andrews, NC; Bertrand, R; Bilodeau, M; Makui, H; Miranda, CJ; Mui, J; Santos, MM; Soares, RJ; Vali, H1
Jin, F; Li, S; Lu, Z; Shi, X; Wan, C; Wang, L; Yang, Z; Zhang, C; Zhang, D; Zhang, P; Zheng, C; Zheng, W1
Chalès, G; Guggenbuhl, P1
Almasy, L; Blangero, J; Buil, A; Fontcuberta, J; Remacha, A; Souto, JC1
Ioannou, GN; Kowdley, KV1
Hartmann, A; Hellerbrand, C; Lock, G; Pöppl, A; Schölmerich, J1
Combrinck, M; Lehmann, DJ; Livesey, KJ; Merryweather-Clarke, AT; Robson, KJ; Smith, AD; Warden, DR; Wimhurst, VL1
Jaschke, WR; Kremser, C; Metzler, B; Pachinger, O; Poelzl, G; Schocke, MF; Steinboeck, P; Vogel, W; Wolf, C; Zoller, H1
Garderet, L; Gorin, NC; Hermelin, B; Rosmorduc, O1
Brigand, A; David, V; Deugnier, Y; Jouannolle, AM; Lafraise, B; Lainé, F; Morcet, J; Mosser, J; Pouchard, M1
De Henauw, S; Debels, L; Delanghe, J; Pynaert, I; Taes, Y; Temmerman, M; Verhasselt, B; Verstraelen, H1
Bradley, M; Dalton, A; Dube, A; Evans, S; Gleeson, D; Jones, J; Peck, RJ; Rigby, E1
Broman, KW; Clothier, B; Davies, R; Edwards, RE; Grant, GR; Judah, DJ; Robinson, SW; Smith, AG1
Binni, F; Cerrone, A; De Bernardo, C; Grammatico, P; Majore, S; Milano, F; Palka, G; Stuppia, L; Tafuri, A1
Arveiler, B; Commenges, D; Dartigues, JF; Duchêne, F; Iron, A; Letenneur, L; Rondeau, V1
Arriola, E; Blázquez, L; Buiza, C; Cuadrado, E; De Juan, D; Emparanza, JI; Etxeberria, I; Lamet, I; López de Munain, A; Martínez-Lage, P; Otaegui, D; Ruiz-Martínez, J; Sáenz, A; Samaranch, L; Sistiaga, A; Urdaneta, E; Yanguas, J1
Arroyo-Pardo, E; Fairweather-Tait, SJ; Lopez-Parra, AM; Navas-Carretero, S; Perez-Granados, AM; Roe, MA; Sarria, B; Teucher, B; Vaquero, MP1
Branko, A; Iidaka, T; Inada, T; Ishihara, R; Ji, X; Maeno, N; Ozaki, N; Saito, S; Takahashi, N; Yoshida, K1
Ekblom, K; Hallmans, G; Hultdin, J; Johansson, I; Johansson, L; Marklund, SL; Stegmayr, B; Van Guelpen, B; Weinehall, L; Wiklund, PG1
Han, Y; Qu, M; Tang, F; Wang, L; Yue, W; Zhang, D1
Crampton, EM; Subramaniam, VN; Summerville, L; Wallace, DF1
Acton, RT; Adams, PC; Barton, JC; Bean, R; Castro, O; Chen, WP; Gordeuk, VR; Harris, EL; McLachlan, GJ; McLaren, CE; Reboussin, DM; Snively, BM; Speechley, M1
Amato, M; Aterini, S; Gulisano, M; Pacini, S; Punzi, T; Ruggiero, M1
Lesch, OM; Walter, H1
Golabi, P; Kapoor, AK; Kshatriya, GK1
Ajioka, RS; Bulaj, ZJ; Edwards, CQ; Franklin, MR; Griffen, LM; Guinee, DJ; Kushner, JP; Phillips, JD1
Jhoo, JH; Kim, KW; Lee, DY; Lee, JH; Lee, KU; Woo, JI; Youn, JY1
Beutler, E; Felitti, V; Halloran, C; Lee, PL; Trevino, R1
Jhoo, JH; Kim, KW; Lee, DY; Lee, JH; Lee, KU; Woo, JI; Youn, JC; Youn, JY1
Ballard, CG; Edwardson, JA; Hussain, RI; Morris, CM1
Bukhari, M; Jennings, BA; Scott, DG; Smith, K; Willis, G; Wimperis, JZ1
Beutler, E; Felitti, V; Gelbart, T; Ho, NJ; Waalen, J1
Izmerov, NF; Kuzmina, LP; Tarasova, LA1

Reviews

9 review(s) available for transferrin and Genetic Predisposition

ArticleYear
Association of transferrin G258A and transferrin receptor A82G polymorphisms with the risk of Parkinson disease in certain area.
    Medicine, 2020, Nov-25, Volume: 99, Issue:48

    Topics: Alleles; Genetic Predisposition to Disease; Genotype; Humans; Models, Genetic; Parkinson Disease; Polymorphism, Single Nucleotide; Receptors, Transferrin; Transferrin

2020
Hereditary hemochromatosis.
    American family physician, 2013, Feb-01, Volume: 87, Issue:3

    Topics: Alanine Transaminase; Algorithms; Aspartate Aminotransferases; Carcinoma, Hepatocellular; Cardiovascular Diseases; Ferritins; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Liver Cirrhosis; Liver Neoplasms; Membrane Proteins; Mutation, Missense; Phlebotomy; Prevalence; Racial Groups; Transferrin

2013
Meta-analysis on the association between the TF gene rs1049296 and AD.
    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2013, Volume: 40, Issue:5

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Bias; Databases, Bibliographic; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Meta-Analysis as Topic; Middle Aged; Polymorphism, Single Nucleotide; Risk; Transferrin

2013
Iron deficiency: new insights into diagnosis and treatment.
    Hematology. American Society of Hematology. Education Program, 2015, Volume: 2015

    Topics: Administration, Oral; Anemia, Iron-Deficiency; Animals; Dietary Supplements; Disease Models, Animal; Female; Ferritins; Genetic Predisposition to Disease; Hematologic Tests; Hematology; Humans; Inflammation; Infusions, Intravenous; Infusions, Parenteral; Iron; Iron Deficiencies; Male; Transferrin

2015
[Diabetic nephropathy--predictive methods].
    Nihon rinsho. Japanese journal of clinical medicine, 2002, Volume: 60 Suppl 10

    Topics: Albuminuria; Animals; Biomarkers; Collagen Type IV; Diabetic Nephropathies; Fibronectins; Fructose; Genetic Predisposition to Disease; Glycation End Products, Advanced; Humans; Hyperglycemia; Hypertension; Predictive Value of Tests; Protein Kinase C; Risk Factors; Sorbitol; Transferrin

2002
The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis.
    Blood, 2003, May-01, Volume: 101, Issue:9

    Topics: Adult; Aged; Amino Acid Substitution; California; Codon; Cohort Studies; Environment; Epistasis, Genetic; Female; Forecasting; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Male; Membrane Proteins; Middle Aged; Mutation, Missense; Norway; Penetrance; Point Mutation; Prevalence; Transferrin

2003
Clinical consequences of iron overload in hemochromatosis homozygotes.
    Blood, 2003, May-01, Volume: 101, Issue:9

    Topics: Adult; Age Distribution; Aged; Amino Acid Substitution; Blood Donors; California; Codon; Female; Ferritins; Genetic Predisposition to Disease; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Homozygote; Humans; Iron; Iron Overload; Male; Mass Screening; Membrane Proteins; Middle Aged; Mutation, Missense; Norway; Observer Variation; Penetrance; Phlebotomy; Point Mutation; Selection Bias; Transferrin

2003
When and how should we screen for hereditary hemochromatosis?
    Joint bone spine, 2003, Volume: 70, Issue:4

    Topics: Genetic Predisposition to Disease; Genetic Testing; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Membrane Proteins; Mutation; Transferrin

2003
New 'state' markers for the detection of alcoholism.
    Alcohol and alcoholism (Oxford, Oxfordshire). Supplement, 1996, Volume: 31, Issue:1

    Topics: Alcohol Drinking; Alcoholism; Biomarkers; Genetic Predisposition to Disease; Humans; Reproducibility of Results; Sensitivity and Specificity; Transferrin

1996

Other Studies

73 other study(ies) available for transferrin and Genetic Predisposition

ArticleYear
A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N-glycans in patient's serum.
    American journal of medical genetics. Part A, 2021, Volume: 185, Issue:11

    Topics: Congenital Disorders of Glycosylation; Female; Genetic Predisposition to Disease; Genetic Testing; Glycosylation; Homozygote; Humans; Infant; Infant, Newborn; Male; Mannosyltransferases; Mutation, Missense; Phenotype; Polysaccharides; Slovakia; Transferrin

2021
Association between vitamin D receptor (FokI) genetic variant rs2228570 and iron profile in hemodialysis patients.
    Molecular biology reports, 2020, Volume: 47, Issue:1

    Topics: Adult; Anemia, Iron-Deficiency; Case-Control Studies; Erythropoietin; Female; Ferritins; Genetic Predisposition to Disease; Humans; Iron; Iron Deficiencies; Male; Middle Aged; Polymorphism, Genetic; Receptors, Calcitriol; Renal Dialysis; Renal Insufficiency, Chronic; Transferrin

2020
Causal associations of iron status with gout and rheumatoid arthritis, but not with inflammatory bowel disease.
    Clinical nutrition (Edinburgh, Scotland), 2020, Volume: 39, Issue:10

    Topics: Arthritis, Rheumatoid; Biomarkers; Ferritins; Genetic Predisposition to Disease; Genome-Wide Association Study; Gout; Humans; Inflammatory Bowel Diseases; Iron; Mendelian Randomization Analysis; Phenotype; Polymorphism, Single Nucleotide; Risk Assessment; Risk Factors; Transferrin

2020
Iron Status and Cancer Risk in UK Biobank: A Two-Sample Mendelian Randomization Study.
    Nutrients, 2020, Feb-19, Volume: 12, Issue:2

    Topics: Adult; Aged; Biological Specimen Banks; Brain Neoplasms; Female; Ferritins; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Iron; Liver Neoplasms; Male; Mendelian Randomization Analysis; Middle Aged; Neoplasms; Nutritional Status; Odds Ratio; Polymorphism, Single Nucleotide; Risk Factors; Transferrin; United Kingdom; White People

2020
Failure to detect synergy between variants in transferrin and hemochromatosis and Alzheimer's disease in large cohort.
    Neurobiology of aging, 2020, Volume: 89

    Topics: Alzheimer Disease; Cohort Studies; Epistasis, Genetic; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Hemochromatosis; Hemochromatosis Protein; Humans; Negative Results; Oxidative Stress; Risk; Transferrin

2020
Frequency of the HAMP (c.-582 A>G) Polymorphism in Iron Deficiency in Saudi Arabia.
    Pakistan journal of biological sciences : PJBS, 2021, Volume: 24, Issue:1

    Topics: Anemia, Iron-Deficiency; Biomarkers; Case-Control Studies; Female; Ferritins; Genetic Association Studies; Genetic Predisposition to Disease; Hepcidins; Humans; Iron; Phenotype; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Saudi Arabia; Transferrin

2021
The Effect of Iron Status on Risk of Coronary Artery Disease: A Mendelian Randomization Study-Brief Report.
    Arteriosclerosis, thrombosis, and vascular biology, 2017, Volume: 37, Issue:9

    Topics: Case-Control Studies; Coronary Artery Disease; Databases, Genetic; Ferritins; Genetic Association Studies; Genetic Predisposition to Disease; Hemochromatosis Protein; Humans; Iron; Iron Metabolism Disorders; Membrane Proteins; Mendelian Randomization Analysis; Odds Ratio; Phenotype; Polymorphism, Single Nucleotide; Protective Factors; Risk Assessment; Risk Factors; Serine Endopeptidases; Transferrin

2017
Investigating the relationship between iron and depression.
    Journal of psychiatric research, 2017, Volume: 94

    Topics: Adolescent; Adult; Australia; Depressive Disorder, Major; Female; Ferritins; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Iron; Linkage Disequilibrium; Male; Queensland; Registries; Transferrin; Young Adult

2017
Blood lead levels, iron metabolism gene polymorphisms and homocysteine: a gene-environment interaction study.
    Occupational and environmental medicine, 2017, Volume: 74, Issue:12

    Topics: Adult; Aged; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Iron; Lead; Male; Middle Aged; Polymorphism, Single Nucleotide; Prospective Studies; Risk Factors; Transferrin

2017
Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation.
    Pediatric research, 2018, Volume: 83, Issue:1-1

    Topics: Adolescent; Adult; Alleles; Case-Control Studies; Child; Child, Preschool; Chromatography, High Pressure Liquid; Congenital Disorders of Glycosylation; Female; Fetal Alcohol Spectrum Disorders; Genetic Predisposition to Disease; Genetic Variation; Glycosylation; Humans; Infant; Male; Maternal Exposure; Middle Aged; Mothers; Mutation; Odds Ratio; Pregnancy; Retrospective Studies; Sequence Analysis, DNA; Transferrin

2018
Iron-related gene variants and brain iron in multiple sclerosis and healthy individuals.
    NeuroImage. Clinical, 2018, Volume: 17

    Topics: Adult; Aged; Brain; Brain Chemistry; Female; Genetic Predisposition to Disease; Genotype; Gray Matter; Hemochromatosis Protein; Humans; Image Interpretation, Computer-Assisted; Iron; Magnetic Resonance Imaging; Male; Middle Aged; Multiple Sclerosis; Polymorphism, Single Nucleotide; Transferrin

2018
Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis.
    BMC medical genetics, 2018, 01-05, Volume: 19, Issue:1

    Topics: Adult; Female; Ferritins; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Homozygote; Humans; Iron; Iron Overload; Male; Middle Aged; Mutation; Quality of Life; Socioeconomic Factors; Surveys and Questionnaires; Transferrin

2018
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases.
    PloS one, 2018, Volume: 13, Issue:3

    Topics: Aged; Aged, 80 and over; Alleles; Alzheimer Disease; Apolipoproteins E; Cation Transport Proteins; Cognitive Dysfunction; Dementia, Vascular; Female; Gene Expression Regulation; Genetic Predisposition to Disease; Hemochromatosis Protein; Hepcidins; Homeostasis; Humans; Iron; Male; Mental Status and Dementia Tests; Polymorphism, Single Nucleotide; Risk Factors; Transferrin

2018
Ten years of screening for congenital disorders of glycosylation in Argentina: case studies and pitfalls.
    Pediatric research, 2018, Volume: 84, Issue:6

    Topics: Adult; Argentina; Child; Child, Preschool; Collagen Type VI; Congenital Disorders of Glycosylation; Exome; Female; Galactosemias; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Glycolipids; Glycoproteins; Glycosylation; Homozygote; Humans; Infant; Infant, Newborn; Isoelectric Focusing; Male; Mass Screening; Neonatal Screening; Phenotype; Sequence Analysis, DNA; Transferrin

2018
Diagnosis and management of hereditary haemochromatosis.
    The British journal of general practice : the journal of the Royal College of General Practitioners, 2013, Volume: 63, Issue:611

    Topics: Female; Ferritins; General Practice; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Male; Membrane Proteins; Phenotype; Prevalence; Referral and Consultation; Transferrin; United Kingdom

2013
Total mortality by elevated transferrin saturation in patients with diabetes.
    Diabetes care, 2013, Volume: 36, Issue:9

    Topics: Adult; Aged; Diabetes Mellitus, Type 1; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Risk Factors; Transferrin

2013
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
    Nature communications, 2014, Oct-29, Volume: 5

    Topics: Adult; Chromosomes, Human, Pair 7; Ferritins; Gene Expression Regulation; Genetic Association Studies; Genetic Loci; Genetic Predisposition to Disease; Hemochromatosis; Homeostasis; Humans; Iron; Lipids; Phenotype; Polymorphism, Single Nucleotide; Reproducibility of Results; Risk Factors; Transferrin

2014
Improved detection of hereditary haemochromatosis.
    Journal of clinical pathology, 2015, Volume: 68, Issue:3

    Topics: Adult; Aged; Algorithms; Biomarkers; Critical Pathways; DNA Mutational Analysis; Female; Ferritins; Genetic Predisposition to Disease; Hemochromatosis; Hemochromatosis Protein; Heredity; Heterozygote; Histocompatibility Antigens Class I; Homozygote; Humans; Laboratories, Hospital; Male; Membrane Proteins; Middle Aged; Mutation; Phenotype; Predictive Value of Tests; Primary Health Care; Referral and Consultation; Transferrin; Up-Regulation

2015
Common Variants and Haplotypes in the TF, TNF-α, and TMPRSS6 Genes Are Associated with Iron Status in a Female Black South African Population.
    The Journal of nutrition, 2015, Volume: 145, Issue:5

    Topics: Adaptor Proteins, Signal Transducing; Adult; Aged; Aged, 80 and over; Alleles; Anemia, Iron-Deficiency; Black People; Cohort Studies; Female; Genetic Association Studies; Genetic Predisposition to Disease; Histocompatibility Antigens Class II; Humans; Membrane Proteins; Middle Aged; Nutritional Status; Polymorphism, Single Nucleotide; Prospective Studies; Receptors, Transferrin; Serine Endopeptidases; Solubility; South Africa; Transferrin; Tumor Necrosis Factor-alpha

2015
Lessons from a survey of genotyping for hereditary haemochromatosis.
    Journal of clinical pathology, 2015, Volume: 68, Issue:7

    Topics: Biomarkers; DNA Mutational Analysis; England; Ferritins; Genetic Markers; Genetic Predisposition to Disease; Health Surveys; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Membrane Proteins; Mutation; Phenotype; Predictive Value of Tests; Risk Factors; Transferrin

2015
Analysis of Familial Tendencies in Transferrin Saturation in a Korean Population.
    Digestive diseases and sciences, 2015, Volume: 60, Issue:10

    Topics: Adolescent; Adult; Age Distribution; Aged; Aged, 80 and over; Asian People; Child; Female; Genetic Predisposition to Disease; Humans; Incidence; Iron Overload; Male; Mass Screening; Middle Aged; Pedigree; Republic of Korea; Risk Assessment; Sex Distribution; Transferrin; White People; Young Adult

2015
Variables Related to Iron Status and Genetic Background Among Korean Populations: Ironing Out the Differences.
    Digestive diseases and sciences, 2015, Volume: 60, Issue:10

    Topics: Female; Genetic Predisposition to Disease; Humans; Iron Overload; Male; Transferrin

2015
BRCA2 gene mutations and coagulation-associated biomarkers.
    Thrombosis and haemostasis, 2016, Volume: 115, Issue:2

    Topics: Adult; alpha 1-Antitrypsin; Binding Sites; Biomarkers; Blood Coagulation; BRCA2 Protein; Breast Neoplasms; Case-Control Studies; DNA Mutational Analysis; Female; Fibrinogen; Genetic Predisposition to Disease; Haptoglobins; Heterozygote; Humans; Middle Aged; Mutation; P-Selectin; Platelet Factor 4; Rad51 Recombinase; Transferrin

2016
Genetic factors influencing ferritin levels in 14,126 blood donors: results from the Danish Blood Donor Study.
    Transfusion, 2016, Volume: 56, Issue:3

    Topics: Adolescent; Adult; Aged; Anemia, Iron-Deficiency; Blood Donors; Female; Ferritins; Genetic Predisposition to Disease; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Logistic Models; Male; Membrane Proteins; Middle Aged; Nerve Tissue Proteins; Polymorphism, Single Nucleotide; Serine Endopeptidases; Transcription Factors; Transferrin; Young Adult

2016
Using iron studies to predict HFE mutations in New Zealand: implications for laboratory testing.
    Internal medicine journal, 2017, Volume: 47, Issue:4

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Clinical Laboratory Techniques; DNA Mutational Analysis; Female; Ferritins; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hemochromatosis Protein; Humans; Iron; Iron Overload; Male; Membrane Proteins; Middle Aged; Mutation; New Zealand; Predictive Value of Tests; Prevalence; Transferrin; Young Adult

2017
HFE gene mutation is a risk factor for tissue iron accumulation in hemodialysis patients.
    Hemodialysis international. International Symposium on Home Hemodialysis, 2017, Volume: 21, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Cross-Sectional Studies; Female; Genetic Predisposition to Disease; Hemochromatosis Protein; Humans; Iron; Iron Overload; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Renal Dialysis; Risk Factors; Transferrin; Young Adult

2017
Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II.
    Molecular genetics and metabolism, 2017, Volume: 120, Issue:3

    Topics: Adolescent; Child; Child, Preschool; Chromatography, High Pressure Liquid; Congenital Disorders of Glycosylation; Exome; Female; Gene Regulatory Networks; Genetic Predisposition to Disease; Genotype; High-Throughput Nucleotide Sequencing; Humans; Infant; Male; Phenotype; Protein Isoforms; Retrospective Studies; Sequence Analysis, DNA; Transferrin

2017
A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.
    British journal of haematology, 2009, Volume: 147, Issue:1

    Topics: Adult; Aged; Cytochrome b Group; Female; Ferritins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Homozygote; Humans; Iron; Male; Membrane Proteins; Middle Aged; Oxidoreductases; Polymorphism, Single Nucleotide; Prospective Studies; Transferrin

2009
HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
    Circulation. Cardiovascular genetics, 2009, Volume: 2, Issue:1

    Topics: Adult; Aged; Alleles; Amino Acid Substitution; Female; Ferritins; Genetic Predisposition to Disease; Haplotypes; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Homozygote; Humans; Iron Overload; Lipoproteins, LDL; Male; Mass Screening; Membrane Proteins; Middle Aged; Polymorphism, Single Nucleotide; Transferrin

2009
Hereditary haemochromatosis: a tale of eight siblings.
    Clinical medicine (London, England), 2009, Volume: 9, Issue:6

    Topics: Biopsy; Diagnosis, Differential; Genetic Predisposition to Disease; Genetic Testing; Hemochromatosis; Humans; Iron; Liver; Male; Middle Aged; Siblings; Transferrin

2009
Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.
    Annals of hematology, 2010, Volume: 89, Issue:8

    Topics: Adolescent; Adult; Aged; Diet; Female; Ferritins; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Iron Overload; Life Style; Male; Mediterranean Region; Membrane Proteins; Middle Aged; Mutation; Polymorphism, Genetic; Spain; Transferrin; Young Adult

2010
Detection of hereditary hemochromatosis and biochemical iron overload in primary care: a multicenter case finding study in Spain.
    American journal of hematology, 2010, Volume: 85, Issue:4

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Female; Ferritins; Follow-Up Studies; Genetic Predisposition to Disease; Genetic Testing; Hemochromatosis; Hemochromatosis Protein; Heterozygote; Histocompatibility Antigens Class I; Humans; Iron Overload; Male; Membrane Proteins; Metabolic Syndrome; Middle Aged; Spain; Transferrin; Young Adult

2010
A pigmented octogenarian.
    Age and ageing, 2010, Volume: 39, Issue:3

    Topics: Aged, 80 and over; Diagnosis, Differential; Female; Genetic Predisposition to Disease; Genetic Testing; Hemochromatosis; Hemosiderin; Humans; Liver Diseases; Phlebotomy; Pigmentation Disorders; Transferrin; Treatment Outcome

2010
HFE genotyping: maximising the value for hemochromatosis patients and families.
    Journal of gastroenterology and hepatology, 2010, Volume: 25, Issue:7

    Topics: Ferritins; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Homozygote; Humans; Iron; Liver; Membrane Proteins; Mutation; Pedigree; Phenotype; Spain; Transferrin; White People

2010
Significance of H63D homozygosity in a Basque population with hemochromatosis.
    Journal of gastroenterology and hepatology, 2010, Volume: 25, Issue:7

    Topics: Adult; Aged; Aged, 80 and over; Biopsy; Female; Ferritins; Gene Frequency; Genetic Predisposition to Disease; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Homozygote; Humans; Iron; Liver; Male; Membrane Proteins; Middle Aged; Mutation; Phenotype; Polymerase Chain Reaction; Porphyria Cutanea Tarda; Retrospective Studies; Spain; Spectrophotometry, Atomic; Transferrin; White People

2010
Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.
    Gastroenterology, 2011, Volume: 140, Issue:7

    Topics: Adult; Antimicrobial Cationic Peptides; Biopsy; Case-Control Studies; Cation Transport Proteins; DNA Mutational Analysis; Ferritins; Genetic Predisposition to Disease; HEK293 Cells; Hepcidins; Humans; Iron; Iron Overload; Liver; Macrophages; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Pedigree; Phenotype; Protein Transport; Transfection; Transferrin

2011
The A Allele of the -576G>A polymorphism of the transferrin gene is associated with the increased risk of age-related macular degeneration in smokers.
    The Tohoku journal of experimental medicine, 2011, Volume: 223, Issue:4

    Topics: Aged; Alleles; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Macular Degeneration; Male; Polymorphism, Single Nucleotide; Risk; Smoking; Transferrin

2011
Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease.
    Neurobiology of aging, 2012, Volume: 33, Issue:8

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Biomarkers; Causality; Comorbidity; Female; Genetic Predisposition to Disease; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Italy; Liver Diseases; Male; Membrane Proteins; Mutation; Polymorphism, Single Nucleotide; Prevalence; Risk Factors; Transferrin

2012
HFE mutations and transferrin C1/C2 polymorphism among Croatian patients with schizophrenia and schizoaffective disorder.
    Molecular biology reports, 2012, Volume: 39, Issue:3

    Topics: Adult; Age of Onset; Croatia; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Male; Membrane Proteins; Middle Aged; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Psychotic Disorders; Regression Analysis; Schizophrenia; Statistics, Nonparametric; Transferrin

2012
TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia.
    Human molecular genetics, 2012, May-01, Volume: 21, Issue:9

    Topics: Aged; Anemia, Iron-Deficiency; Asian People; Bone Morphogenetic Protein 2; Case-Control Studies; China; Cohort Studies; Female; Genetic Predisposition to Disease; Hemoglobins; Humans; Membrane Proteins; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Transferrin; Risk Factors; Serine Endopeptidases; Transferrin

2012
Genetic determinants for body iron store and type 2 diabetes risk in US men and women.
    PloS one, 2012, Volume: 7, Issue:7

    Topics: Adult; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Follow-Up Studies; Genetic Association Studies; Genetic Predisposition to Disease; Health Personnel; Heme; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Male; Membrane Proteins; Polymorphism, Single Nucleotide; Risk Factors; Transferrin; United States

2012
Unsaturated iron binding capacity and transferrin saturation are equally reliable in detection of HFE hemochromatosis.
    The American journal of gastroenterology, 2002, Volume: 97, Issue:8

    Topics: Bayes Theorem; Ferritins; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Humans; Iron; Logistic Models; Mutation; Predictive Value of Tests; ROC Curve; Sensitivity and Specificity; Transferrin

2002
Hfe deficiency increases susceptibility to cardiotoxicity and exacerbates changes in iron metabolism induced by doxorubicin.
    Blood, 2003, Oct-01, Volume: 102, Issue:7

    Topics: Alanine Transaminase; Animals; Antibiotics, Antineoplastic; Aspartate Aminotransferases; Creatine Kinase; Doxorubicin; Female; Genetic Predisposition to Disease; Hemochromatosis Protein; Histocompatibility Antigens Class I; Iron; Iron Metabolism Disorders; Liver; Membrane Proteins; Mice; Mice, Mutant Strains; Mitochondria; Myocardium; Survival Rate; Transferrin

2003
Association study between late-onset Alzheimer's disease and the transferrin gene polymorphisms in Chinese.
    Neuroscience letters, 2003, Oct-09, Volume: 349, Issue:3

    Topics: Age Factors; Aged; Alzheimer Disease; Apolipoprotein E4; Apolipoproteins E; Brain; Brain Chemistry; China; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Polymorphism, Genetic; Risk Factors; Transferrin

2003
Genetic determinants of iron metabolism plasma phenotypes and their relationship with risk of thrombosis.
    Haematologica, 2003, Volume: 88, Issue:12

    Topics: Biomarkers; Cohort Studies; Ferritins; Genetic Predisposition to Disease; Humans; Iron; Phenotype; Receptors, Transferrin; Risk; Spain; Thrombophilia; Thrombosis; Transferrin

2003
Iron, HFE mutations, and hepatocellular carcinoma: is hepatic iron a carcinogen?
    Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2003, Volume: 1, Issue:4

    Topics: Biomarkers, Tumor; Carcinoma, Hepatocellular; Ferritins; Genetic Predisposition to Disease; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Liver; Liver Cirrhosis; Liver Neoplasms; Loss of Heterozygosity; Membrane Proteins; Mutation; Siderosis; Transferrin

2003
HFE C282Y heterozygosity in hepatocellular carcinoma: evidence for an increased prevalence.
    Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2003, Volume: 1, Issue:4

    Topics: Biomarkers, Tumor; Carcinoma, Hepatocellular; Female; Ferritins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Germany; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Liver; Liver Cirrhosis; Liver Neoplasms; Loss of Heterozygosity; Male; Membrane Proteins; Middle Aged; Prevalence; Risk Factors; Severity of Illness Index; Siderosis; Statistics as Topic; Transferrin

2003
Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.
    Journal of medical genetics, 2004, Volume: 41, Issue:4

    Topics: Aged; Alleles; Alzheimer Disease; Apolipoprotein E4; Apolipoproteins E; Case-Control Studies; Cognition Disorders; Female; Genetic Predisposition to Disease; Genotype; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Male; Membrane Proteins; Oxidative Stress; Polymorphism, Genetic; Transferrin

2004
Cardiac phosphorus-31 two-dimensional chemical shift imaging in patients with hereditary hemochromatosis.
    Magnetic resonance imaging, 2004, Volume: 22, Issue:4

    Topics: Adenosine Triphosphate; Adult; Biomarkers; Cholesterol, LDL; Echocardiography; Electrocardiography; Ferritins; Genetic Predisposition to Disease; Heart Diseases; Heart Ventricles; Hemochromatosis; Homozygote; Humans; Iron; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Phosphocreatine; Phosphorus Isotopes; Transferrin; Triglycerides

2004
Hereditary hyperferritinemia-cataract syndrome: a novel mutation in the iron-responsive element of the L-ferritin gene in a French family.
    The American journal of medicine, 2004, Jul-15, Volume: 117, Issue:2

    Topics: Adult; Apoferritins; Cataract; Family Health; Female; Ferritins; Genetic Predisposition to Disease; Humans; Iron; Iron-Regulatory Proteins; Pedigree; Point Mutation; Syndrome; Transferrin

2004
Phenotypic expression in detected C282Y homozygous women depends on body mass index.
    Journal of hepatology, 2005, Volume: 43, Issue:6

    Topics: Adult; Aged; Body Mass Index; Female; Gene Expression; Genetic Predisposition to Disease; Genetic Testing; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Homozygote; Humans; Male; Membrane Proteins; Middle Aged; Mutation; Phenotype; Sex Factors; Transferrin

2005
Human transferrin G277S mutation and iron deficiency in pregnancy.
    British journal of haematology, 2006, Volume: 132, Issue:2

    Topics: Adult; Anemia, Iron-Deficiency; Female; Genetic Predisposition to Disease; Humans; Mutation; Pregnancy; Pregnancy Complications, Hematologic; Transferrin

2006
HFE genotypes in decompensated alcoholic liver disease: phenotypic expression and comparison with heavy drinking and with normal controls.
    The American journal of gastroenterology, 2006, Volume: 101, Issue:2

    Topics: Alcohol Drinking; Blood Donors; Disease Progression; DNA; Female; Ferritins; Gene Expression; Genetic Predisposition to Disease; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Liver Diseases, Alcoholic; Male; Membrane Proteins; Middle Aged; Mutation; Phenotype; Polymerase Chain Reaction; Risk Factors; Severity of Illness Index; Transferrin

2006
Multiple polymorphic loci determine basal hepatic and splenic iron status in mice.
    Hepatology (Baltimore, Md.), 2006, Volume: 44, Issue:1

    Topics: Animals; Chromosomes, Mammalian; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Iron; Liver; Mice; Mice, Inbred C57BL; Polymorphism, Genetic; Quantitative Trait Loci; RNA, Messenger; Spleen; Transferrin

2006
Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
    Haematologica, 2006, Volume: 91, Issue:8 Suppl

    Topics: Adult; DNA Mutational Analysis; Family; Female; Genetic Predisposition to Disease; Hemochromatosis; Humans; Iron Overload; Italy; Male; Receptors, Transferrin; Transferrin

2006
Analysis of the effect of aluminum in drinking water and transferrin C2 allele on Alzheimer's disease.
    European journal of neurology, 2006, Volume: 13, Issue:9

    Topics: Aged; Aged, 80 and over; Alleles; Aluminum; Alzheimer Disease; Apolipoproteins E; Case-Control Studies; Chi-Square Distribution; Cohort Studies; Environmental Exposure; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Logistic Models; Male; Neurotoxins; Polymorphism, Genetic; Retrospective Studies; Risk; Transferrin

2006
Genes related to iron metabolism and susceptibility to Alzheimer's disease in Basque population.
    Neurobiology of aging, 2007, Volume: 28, Issue:12

    Topics: Aged; Alzheimer Disease; Comorbidity; Female; Genetic Predisposition to Disease; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron Metabolism Disorders; Male; Membrane Proteins; Prevalence; Risk Assessment; Risk Factors; Spain; Transferrin

2007
The G277S transferrin mutation does not affect iron absorption in iron deficient women.
    European journal of nutrition, 2007, Volume: 46, Issue:1

    Topics: Adult; Anemia, Iron-Deficiency; Female; Genetic Predisposition to Disease; Humans; Iron Deficiencies; Iron, Dietary; Middle Aged; Mutation; Pilot Projects; Polymorphism, Genetic; Risk Factors; Transferrin

2007
Association study between the transferrin gene and schizophrenia in the Japanese population.
    Neuroreport, 2007, Mar-26, Volume: 18, Issue:5

    Topics: Adult; Aged; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Japan; Male; Middle Aged; Polymorphism, Single Nucleotide; Schizophrenia; Transferrin

2007
Iron stores and HFE genotypes are not related to increased risk of ischemic stroke. A prospective nested case-referent study.
    Cerebrovascular diseases (Basel, Switzerland), 2007, Volume: 24, Issue:5

    Topics: Adult; Aged; Brain Ischemia; Case-Control Studies; Cerebral Hemorrhage; Female; Ferritins; Genetic Predisposition to Disease; Health Surveys; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Iron; Iron-Binding Proteins; Male; Membrane Proteins; Middle Aged; Odds Ratio; Phenotype; Prospective Studies; Risk Assessment; Risk Factors; Sex Factors; Stroke; Surveys and Questionnaires; Sweden; Transferrin

2007
Polymorphisms of Transferrin gene are associated with schizophrenia in Chinese Han population.
    Journal of psychiatric research, 2008, Volume: 42, Issue:11

    Topics: Adult; Alleles; Asian People; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Introns; Linkage Disequilibrium; Male; Polymorphism, Single Nucleotide; Schizophrenia; Transferrin

2008
Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosis.
    American journal of physiology. Cell physiology, 2008, Volume: 294, Issue:2

    Topics: Animals; Cell Compartmentation; Cell Line; Cell Membrane; Genetic Predisposition to Disease; Hemochromatosis; Hepatocytes; Humans; Iron; Mice; Mutation; Protein Transport; Receptors, Transferrin; Transferrin; Transport Vesicles

2008
Bivariate mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americans, Hispanics, and whites in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.
    Translational research : the journal of laboratory and clinical medicine, 2008, Volume: 151, Issue:2

    Topics: Canada; Comorbidity; Female; Ferritins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Humans; Iron Overload; Male; Models, Genetic; Odds Ratio; Racial Groups; Transferrin; United States

2008
Iron indices and vitamin D receptor polymorphisms in hemodialysis patients.
    Advances in chronic kidney disease, 2008, Volume: 15, Issue:2

    Topics: Adult; Aged; Anemia, Iron-Deficiency; Biomarkers; Female; Ferritins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Iron; Kidney Failure, Chronic; Male; Middle Aged; Polymorphism, Genetic; Predictive Value of Tests; Receptors, Calcitriol; Renal Dialysis; Transferrin

2008
Association of genetic markers with coronary heart disease (myocardial infarction)--a case-control study.
    Journal of the Indian Medical Association, 1999, Volume: 97, Issue:1

    Topics: Case-Control Studies; Complement C3; Coronary Disease; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Haptoglobins; Humans; India; Myocardial Infarction; Phenotype; Polymorphism, Genetic; Transferrin

1999
Hemochromatosis genes and other factors contributing to the pathogenesis of porphyria cutanea tarda.
    Blood, 2000, Mar-01, Volume: 95, Issue:5

    Topics: Adolescent; Adult; Alcohol Drinking; Biopsy; Child, Preschool; Comorbidity; Estrogens; Female; Ferritins; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hepatitis C; Humans; Iron; Liver; Male; Middle Aged; Point Mutation; Polymerase Chain Reaction; Porphyria Cutanea Tarda; Transferrin

2000
Transferrin C2 variant does not confer a risk for Alzheimer's disease in Koreans.
    Neuroscience letters, 2001, Jul-27, Volume: 308, Issue:1

    Topics: Age Factors; Aged; Alzheimer Disease; Apolipoproteins E; Chromosome Mapping; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Korea; Linkage Disequilibrium; Male; Polymorphism, Genetic; Sex Factors; Transferrin

2001
Human transferrin G277S mutation: a risk factor for iron deficiency anaemia.
    British journal of haematology, 2001, Volume: 115, Issue:2

    Topics: Adult; Amino Acid Sequence; Anemia, Iron-Deficiency; Animals; Female; Genetic Predisposition to Disease; Genotype; Humans; Iron; Male; Middle Aged; Point Mutation; Polymorphism, Genetic; Risk Factors; Species Specificity; Transferrin

2001
Neither the butyrylcholinesterase K variant nor transferrin C2 variant confers a risk for Alzheimer's disease in Koreans.
    Journal of neural transmission (Vienna, Austria : 1996), 2001, Volume: 108, Issue:10

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Analysis of Variance; Butyrylcholinesterase; Chi-Square Distribution; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Haplotypes; Humans; Korea; Linkage Disequilibrium; Male; Transferrin

2001
Transferrin gene polymorphism in Alzheimer's disease and dementia with Lewy bodies in humans.
    Neuroscience letters, 2002, Jan-04, Volume: 317, Issue:1

    Topics: Aged; Alzheimer Disease; Apolipoprotein E4; Apolipoproteins E; Brain; DNA Mutational Analysis; Free Radicals; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Iron; Lewy Body Disease; Middle Aged; Neurons; Oxidative Stress; Polymorphism, Genetic; Transferrin

2002
HFE mutations in an inflammatory arthritis population.
    Rheumatology (Oxford, England), 2002, Volume: 41, Issue:2

    Topics: Adult; Aged; Arthritis; Female; Ferritins; Genetic Predisposition to Disease; Genotype; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; HLA Antigens; HLA-A Antigens; Homozygote; Humans; Iron; Male; Membrane Proteins; Middle Aged; Mutation; Prevalence; Transferrin

2002
Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene.
    Mayo Clinic proceedings, 2002, Volume: 77, Issue:6

    Topics: Adult; Aged; Aspartic Acid; Case-Control Studies; Cysteine; Double-Blind Method; Female; Ferritins; Genetic Predisposition to Disease; Genetic Testing; Genotype; Hemochromatosis; Hispanic or Latino; Histidine; Homozygote; Humans; Male; Middle Aged; Mutation; Prevalence; Surveys and Questionnaires; Transferrin; Tyrosine; United States; White People

2002
Genetic-biochemical criteria for individual sensitivity in development of occupational bronchopulmonary diseases.
    Central European journal of public health, 2002, Volume: 10, Issue:1-2

    Topics: Alleles; Asthma; Case-Control Studies; Complement C3; Genetic Predisposition to Disease; Haptoglobins; Humans; Lactoylglutathione Lyase; Moscow; Occupational Diseases; Occupational Exposure; Phenotype; Phosphoglucomutase; Polymorphism, Genetic; Silicosis; Transferrin

2002