Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and AHI1[original query] |
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Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.
American journal of human genetics 2007 Aug 81 (2): 338-45. Salonen Jukka T, Uimari Pekka, Aalto Juha-Matti, Pirskanen Mia, Kaikkonen Jari, Todorova Boryana, Hyppönen Jelena, Korhonen Veli-Pekka, Asikainen Janne, Devine Christopher, Tuomainen Tomi-Pekka, Luedemann Jan, Nauck Matthias, Kerner Wolfgang, Stephens Richard H, New John P, Ollier William E, Gibson J Martin, Payton Antony, Horan Michael A, Pendleton Neil, Mahoney Walt, Meyre David, Delplanque Jerôme, Froguel Philippe, Luzzatto Oren, Yakir Benjamin, Darvasi Ari |
| Association of common variants in the Joubert syndrome gene (AHI1) with autism. Human molecular genetics 2008 Dec 17 (24): 3887-96. Alvarez Retuerto Ana I, Cantor Rita M, Gleeson Joseph G, Ustaszewska Anna, Schackwitz Wendy S, Pennacchio Len A, Geschwind Daniel |
| Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Oct 150B (7): 914-25. Alkelai A, Kohn Y, Olender T, Sarner-Kanyas K, Rigbi A, Hamdan A, Ben-Asher E, Lancet D, Lerer |
| Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Apr 17 (4): 271-8. Huang Xiu-Feng, Huang Fang, Wu Kun-Chao, Wu Juan, Chen Jie, Pang Chi-Pui, Lu Fan, Qu Jia, Jin Zi-Bi |
| Joubert syndrome: genotyping a Northern European patient cohort. European journal of human genetics : EJHG 2015 Apr . Kroes Hester Y, Monroe Glen R, van der Zwaag Bert, Duran Karen J, de Kovel Carolien G, van Roosmalen Mark J, Harakalova Magdalena, Nijman Ies J, Kloosterman Wigard P, Giles Rachel H, Knoers Nine Vam, van Haaften Gi |
| A cis-eQTL in AHI1 confers risk to schizophrenia in European populations. Neuroscience letters 2016 Aug 632 130-135. Ren Zhimin, Qiu Anli, Zhang Aiqi, Huang Lijun, Rao Shuqu |
| Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci. Arthritis & rheumatology (Hoboken, N.J.) 2017 Jul . McIntosh Laura A, Marion Miranda C, Sudman Marc, Comeau Mary E, Becker Mara L, Bohnsack John F, Fingerlin Tasha E, Griffin Thomas A, Haas J Peter, Lovell Daniel J, Maier Lisa A, Nigrovic Peter A, Prahalad Sampath, Punaro Marilynn, Rosé Carlos D, Wallace Carol A, Wise Carol A, , , , , , , Moncrieffe Halima, Howard Timothy D, Langefeld Carl D, Thompson Susan |
| The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults. Multiple sclerosis and related disorders 2018 Jan 19 161-165. Graves Jennifer S, Barcellos Lisa F, Simpson Steve, Belman Anita, Lin Rui, Taylor Bruce V, Ponsonby Anne-Louise, Dwyer Terence, Krupp Lauren, Waubant Emmanuelle, van der Mei Ingrid A |
| Clinical and Molecular Diagnosis of Joubert Syndrome and Related Disorders. Pediatric neurology 2020 3 106 43-49. Radha Rama Devi Akella, Naushad Shaik Mohammad, Lingappa Loke |
| Common Risk Variants in AHI1 Are Associated With Childhood Steroid Sensitive Nephrotic Syndrome. Kidney international reports 2023 8 8 (8): 1562-1574. Mallory L Downie, Sanjana Gupta, Catalin Voinescu, Adam P Levine, Omid Sadeghi-Alavijeh, Stephanie Dufek-Kamperis, Jingjing Cao, Martin Christian, Jameela A Kari, Shenal Thalgahagoda, Randula Ranawaka, Asiri Abeyagunawardena, Rasheed Gbadegesin, Rulan Parekh, Robert Kleta, Detlef Bockenhauer, Horia C Stanescu, Daniel P Ga |
| Role of Abelson Helper Integration Site 1, Nebulin, and Paired Box 3 Genes in the Development of Nonsyndromic Strabismus in a Series of Iranian Families: Sequence Analysis and Systematic Review of the Genetics of Nonsyndromic Strabismus. Journal of current ophthalmology 2024 4 35 (3): 216-225. Maliheh Rahpeyma, Aliakbar Sabermoghaddam, Mohammad Yaser Kiarudi, Amirsaeed Sabeti Aghabozorgi, Alireza Pasd |
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