apnea has been researched along with Genetic Predisposition in 12 studies
Apnea: A transient absence of spontaneous respiration.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Brainstem apolipoprotein AII (apoa2) mRNA expression correlates with apnea in breathing present in the adult C57Bl/6J (B6) sleep apnea model." | 7.85 | C57BL/6J mouse apolipoprotein A2 gene is deterministic for apnea. ( Azzam, S; Darrah, R; Decker, MJ; Dick, TE; Dutschmann, M; Gillombardo, CB; Han, F; Kong, N; Moore, M; Strohl, KP; Yamauchi, M, 2017) |
| "We report a case of X-linked alpha-thalassemia/mental retardation syndrome (ATR-X) with repeated apnea attacks dating from the patient's 12th year." | 7.79 | [A case of X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome with repeated apnea attacks due to laryngomalacia]. ( Ebishima, Y; Misaki, T; Okuno, T; Owa, K; Suehiro, Y; Wada, T, 2013) |
| "Apnea of prematurity (AOP) is a disturbance in respiratory rhythm defined by idiopathic pauses in breathing that reduce blood oxygen levels and/or heart rate." | 7.76 | Heritability of apnea of prematurity: a retrospective twin study. ( Bednarek, F; Bloch-Salisbury, E; Boyd, T; Hall, MH; Paydarfar, D; Sharma, P, 2010) |
| " Patients with BChE deficiency are possibly in danger of postanesthetic apnea." | 3.88 | A novel mutation in the BCHE gene and phenotype identified in a child with low butyrylcholinesterase activity: a case report. ( Dan, Y; Deng, G; Guo, Y; Mao, Q; Tan, W; Yu, R, 2018) |
| "Brainstem apolipoprotein AII (apoa2) mRNA expression correlates with apnea in breathing present in the adult C57Bl/6J (B6) sleep apnea model." | 3.85 | C57BL/6J mouse apolipoprotein A2 gene is deterministic for apnea. ( Azzam, S; Darrah, R; Decker, MJ; Dick, TE; Dutschmann, M; Gillombardo, CB; Han, F; Kong, N; Moore, M; Strohl, KP; Yamauchi, M, 2017) |
| " Breathing frequency variation and central apnea in a group of Mecp2(+/-) females displayed a distribution pattern similar to Mecp2(-/Y) males, while the rest resembled the wild-type mice." | 3.81 | Breathing abnormalities in a female mouse model of Rett syndrome. ( Cui, N; Jiang, C; Johnson, CM; Oginsky, MF; Zhong, W, 2015) |
| "We report a case of X-linked alpha-thalassemia/mental retardation syndrome (ATR-X) with repeated apnea attacks dating from the patient's 12th year." | 3.79 | [A case of X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome with repeated apnea attacks due to laryngomalacia]. ( Ebishima, Y; Misaki, T; Okuno, T; Owa, K; Suehiro, Y; Wada, T, 2013) |
| " He had seizures attacks and apnea from the second week of his life." | 3.78 | Early-onset severe obesity with ACTH deficiency and red hair in a boy: the POMC deficiency. ( Aldemir, O; Ozen, S, 2012) |
| "Apnea of prematurity (AOP) is a disturbance in respiratory rhythm defined by idiopathic pauses in breathing that reduce blood oxygen levels and/or heart rate." | 3.76 | Heritability of apnea of prematurity: a retrospective twin study. ( Bednarek, F; Bloch-Salisbury, E; Boyd, T; Hall, MH; Paydarfar, D; Sharma, P, 2010) |
| "Most sleep disorders run in families and in several of them the contribution of genetic factors is increasingly recognised." | 1.33 | Genetics of narcolepsy and other major sleep disorders. ( Maret, S; Tafti, M, 2005) |
| "Alexander disease is a rare, sporadic leukoencephalopathy characterized by white-matter abnormalities with frontal predominance and, as a rule, clinically associated with megalencephaly, seizures, spasticity, and psychomotor deterioration." | 1.33 | Unusual diagnosis in a child suffering from juvenile Alexander disease: clinical and imaging report. ( Bernardi, B; Bracceschi, R; Colonnelli, MC; Errani, A; Franzoni, E; Garone, C; Malaspina, E; Moscano, FC; Salomons, GS; Sarajlija, J; Van der Knaap, MS; Zimmerman, RA, 2006) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (33.33) | 29.6817 |
| 2010's | 8 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yu, R | 1 |
| Guo, Y | 1 |
| Dan, Y | 1 |
| Tan, W | 1 |
| Mao, Q | 1 |
| Deng, G | 1 |
| Ozen, S | 1 |
| Aldemir, O | 1 |
| Ebishima, Y | 1 |
| Misaki, T | 1 |
| Owa, K | 1 |
| Okuno, T | 1 |
| Wada, T | 1 |
| Suehiro, Y | 1 |
| Johnson, CM | 1 |
| Cui, N | 1 |
| Zhong, W | 1 |
| Oginsky, MF | 1 |
| Jiang, C | 1 |
| Gillombardo, CB | 1 |
| Darrah, R | 1 |
| Dick, TE | 1 |
| Moore, M | 1 |
| Kong, N | 1 |
| Decker, MJ | 1 |
| Han, F | 1 |
| Yamauchi, M | 1 |
| Dutschmann, M | 1 |
| Azzam, S | 1 |
| Strohl, KP | 1 |
| Kaback, M | 1 |
| Lopatequi, J | 1 |
| Portuges, AR | 1 |
| Quindipan, C | 1 |
| Pariani, M | 1 |
| Salimpour-Davidov, N | 1 |
| Rimoin, DL | 1 |
| Bloch-Salisbury, E | 1 |
| Hall, MH | 1 |
| Sharma, P | 1 |
| Boyd, T | 1 |
| Bednarek, F | 1 |
| Paydarfar, D | 1 |
| Pandit, JJ | 1 |
| Gopa, S | 1 |
| Arora, J | 1 |
| Cummings, KJ | 1 |
| Pendlebury, JD | 1 |
| Sherwood, NM | 1 |
| Wilson, RJ | 1 |
| Maret, S | 1 |
| Tafti, M | 1 |
| Franzoni, E | 1 |
| Van der Knaap, MS | 1 |
| Errani, A | 1 |
| Colonnelli, MC | 1 |
| Bracceschi, R | 1 |
| Malaspina, E | 1 |
| Moscano, FC | 1 |
| Garone, C | 1 |
| Sarajlija, J | 1 |
| Zimmerman, RA | 1 |
| Salomons, GS | 1 |
| Bernardi, B | 1 |
| Günther, G | 1 |
| Junker, R | 1 |
| Sträter, R | 1 |
| Schobess, R | 1 |
| Kurnik, K | 1 |
| Heller, C | 1 |
| Kosch, A | 1 |
| Nowak-Göttl, U | 1 |
1 trial available for apnea and Genetic Predisposition
| Article | Year |
|---|---|
Symptomatic ischemic stroke in full-term neonates : role of acquired and genetic prothrombotic risk factors.
Topics: Apnea; Blood Coagulation Disorders; Brain Ischemia; Case-Control Studies; Cerebrovascular Disorders; | 2000 |
11 other studies available for apnea and Genetic Predisposition
| Article | Year |
|---|---|
A novel mutation in the BCHE gene and phenotype identified in a child with low butyrylcholinesterase activity: a case report.
Topics: Adolescent; Apnea; Butyrylcholinesterase; Exons; Genetic Predisposition to Disease; Heterozygote; Hu | 2018 |
Early-onset severe obesity with ACTH deficiency and red hair in a boy: the POMC deficiency.
Topics: Adrenal Insufficiency; Adrenocorticotropic Hormone; Anti-Inflammatory Agents; Apnea; Caloric Restric | 2012 |
[A case of X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome with repeated apnea attacks due to laryngomalacia].
Topics: alpha-Thalassemia; Apnea; Child; Genetic Predisposition to Disease; Humans; Intellectual Disability; | 2013 |
Breathing abnormalities in a female mouse model of Rett syndrome.
Topics: Administration, Inhalation; Age Factors; Animals; Apnea; Carbon Dioxide; Disease Models, Animal; Fem | 2015 |
C57BL/6J mouse apolipoprotein A2 gene is deterministic for apnea.
Topics: Animals; Apnea; Apolipoprotein A-II; Brain Stem; Disease Models, Animal; Genetic Predisposition to D | 2017 |
Genetic screening in the Persian Jewish community: A pilot study.
Topics: Apnea; Butyrylcholinesterase; Cholinesterases; Consanguinity; Drug Hypersensitivity; Ethnicity; Gene | 2010 |
Heritability of apnea of prematurity: a retrospective twin study.
Topics: Apnea; Diseases in Twins; Female; Genetic Predisposition to Disease; Humans; Infant, Newborn; Infant | 2010 |
A hypothesis to explain the high prevalence of pseudo-cholinesterase deficiency in specific population groups.
Topics: Anesthesia; Anesthetics; Animals; Apnea; Butyrylcholinesterase; Cholinesterases; Drug Hypersensitivi | 2011 |
Sudden neonatal death in PACAP-deficient mice is associated with reduced respiratory chemoresponse and susceptibility to apnoea.
Topics: Animals; Animals, Newborn; Apnea; Chemoreceptor Cells; Death, Sudden; Genetic Predisposition to Dise | 2004 |
Genetics of narcolepsy and other major sleep disorders.
Topics: Apnea; Genetic Predisposition to Disease; Humans; Narcolepsy; Sleep Wake Disorders; Switzerland | 2005 |
Unusual diagnosis in a child suffering from juvenile Alexander disease: clinical and imaging report.
Topics: Adolescent; Age of Onset; Alexander Disease; Anorexia; Apnea; Brain; Brain Stem; Child; Deglutition | 2006 |