Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: 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 |
Support for involvement of the AHI1 locus in schizophrenia. European journal of human genetics : EJHG 2007 Sep 15 (9): 988-91. Ingason Andres, Sigmundsson Thordur, Steinberg Stacy, Sigurdsson Engilbert, Haraldsson Magnus, Magnusdottir Brynja B, Frigge Michael L, Kong Augustine, Gulcher Jeffrey, Thorsteinsdottir Unnur, Stefansson Kari, Petursson Hannes, Stefansson Hrei |
High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations. Journal of the American Society of Nephrology : JASN 2007 May 18 (5): 1566-75. Tory Kálmán, Lacoste Tiphanie, Burglen Lydie, Morinière Vincent, Boddaert Nathalie, Macher Marie-Alice, Llanas Brigitte, Nivet Hubert, Bensman Albert, Niaudet Patrick, Antignac Corinne, Salomon Rémi, Saunier Soph |
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 |
Polymorphisms in AHI1 are not associated with type 2 diabetes or related phenotypes in Danes: non-replication of a genome-wide association result. Diabetologia 2008 Apr 51 (4): 609-14. Holmkvist J, Anthonsen S, Wegner L, Andersen G, Jørgensen T, Borch-Johnsen K, Sandbaek A, Lauritzen T, Pedersen O, Hansen |
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 |
Impact of the AHI1 gene on the vulnerability to schizophrenia: a case-control association study. PloS one 2010 5 (8): e12254. Rivero Olga, Reif Andreas, Sanjuán Julio, Moltó María D, Kittel-Schneider Sarah, Nájera Carmen, Töpner Theresia, Lesch Klaus-Pet |
Lymphoblast and brain expression of AHI1 and the novel primate-specific gene, C6orf217, in schizophrenia and bipolar disorder. Schizophrenia research 2010 Jul 120 (1-3): 159-66. Slonimsky Alexandra, Levy Itzchak, Kohn Yoav, Rigbi Amihai, Ben-Asher Edna, Lancet Doron, Agam Galila, Lerer Berna |
Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2010 Aug 24 (8): 3066-82. Torri Federica, Akelai Anna, Lupoli Sara, Sironi Manuela, Amann-Zalcenstein Daniela, Fumagalli Matteo, Dal Fiume Chiara, Ben-Asher Edna, Kanyas Kyra, Cagliani Rachele, Cozzi Paolo, Trombetti Gabriele, Strik Lievers Luisa, Salvi Erika, Orro Alessandro, Beckmann Jacques S, Lancet Doron, Kohn Yoav, Milanesi Luciano, Ebstein Richard B, Lerer Bernard, Macciardi Fab |
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy. Journal of medical genetics 2011 Feb 48 (2): 105-16. Otto Edgar A, Ramaswami Gokul, Janssen Sabine, Chaki Moumita, Allen Susan J, Zhou Weibin, Airik Rannar, Hurd Toby W, Ghosh Amiya K, Wolf Matthias T, Hoppe Bernd, Neuhaus Thomas J, Bockenhauer Detlef, Milford David V, Soliman Neveen A, Antignac Corinne, Saunier Sophie, Johnson Colin A, Hildebrandt Friedhelm, |
The characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndrome. Metabolism: clinical and experimental 2010 1 59 (7): 1057-64. Prior Matthew J, Foletta Victoria C, Jowett Jeremy B, Segal David H, Carless Melanie A, Curran Joanne E, Dyer Tom D, Moses Eric K, McAinch Andrew J, Konstantopoulos Nicky, Bozaoglu Kiymet, Collier Greg R, Cameron-Smith David, Blangero John, Walder Ken |
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Human molecular genetics 2010 Apr 19 (7): 1379-86. Ingason Andrés, Giegling Ina, Cichon Sven, Hansen Thomas, Rasmussen Henrik B, Nielsen Jimmi, Jürgens Gesche, Muglia Pierandrea, Hartmann Annette M, Strengman Eric, Vasilescu Catalina, Mühleisen Thomas W, Djurovic Srdjan, Melle Ingrid, Lerer Bernard, Möller Hans-Jürgen, Francks Clyde, Pietiläinen Olli P H, Lonnqvist Jouko, Suvisaari Jaana, Tuulio-Henriksson Annamari, Walshe Muriel, Vassos Evangelos, Di Forti Marta, Murray Robin, Bonetto Chiara, Tosato Sarah, , Cantor Rita M, Rietschel Marcella, Craddock Nick, Owen Michael J, Peltonen Leena, Andreassen Ole A, Nöthen Markus M, St Clair David, Ophoff Roel A, O'Donovan Michael C, Collier David A, Werge Thomas, Rujescu D |
Association of copy number variation in the AHI1 gene with risk of obesity in the Chinese population. European journal of endocrinology / European Federation of Endocrine Societies 2012 Apr 166 (4): 727-34. Huang Liansha, Teng Dacai, Wang Hao, Sheng Guoqing, Liu Tongh |
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 |
The influence of AHI1 variants on the diagnosis and treatment outcome in schizophrenia. International journal of molecular sciences 2015 16 (2): 2517-29. Porcelli Stefano, Pae Chi-Un, Han Changsu, Lee Soo-Jung, Patkar Ashwin A, Masand Prakash S, Balzarro Beatrice, Alberti Siegfried, De Ronchi Diana, Serretti Alessand |
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 |
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.
Nature genetics 2016 Nov 48 (11): 1425-1429. Bronson Paola G, Chang Diana, Bhangale Tushar, Seldin Michael F, Ortmann Ward, Ferreira Ricardo C, Urcelay Elena, Pereira Luis Fernández, Martin Javier, Plebani Alessandro, Lougaris Vassilios, Friman Vanda, Freiberger Tomáš, Litzman Jiri, Thon Vojtech, Pan-Hammarström Qiang, Hammarström Lennart, Graham Robert R, Behrens Timothy |
Attempts to replicate genetic associations with schizophrenia in a cohort from north India. NPJ schizophrenia 2017 Aug 3 (1): 28. Prasad Suman, Bhatia Triptish, Kukshal Prachi, Nimgaonkar Vishwajit L, Deshpande Smita N, Thelma B |
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 |
MS AHI1 genetic risk promotes IFN? CD4 T cells. Neurology(R) neuroimmunology & neuroinflammation 2018 Jan 5 (1): e414. Kaskow Belinda J, Buttrick Thomas S, Klein Hans-Ulrich, White Charles, Bourgeois Justin R, Ferland Russell J, Patsopoulos Nikolaos, Bradshaw Elizabeth M, De Jager Philip L, Elyaman Wass |
Clarification of undiagnosed ataxia using whole-exome sequencing with clinical implications. Parkinsonism & related disorders 2020 9 80 58-64. Kim Minkyeong, Kim Ah Reum, Kim Ji Sun, Park Jongkyu, Youn Jinyoung, Ahn Jong Hyeon, Mun Jun Kyu, Lee Chung, Kim Nam-Soon, Kim Nayoung K D, Park Woong-Yang, Cho Jin Wh |
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 |
Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum. Molecular biology reports 2021 6 48 (6): 5339-5345. Karamzade Arezou, Babaei Meisam, Saberi Mohammad, Golchin Neda, Khalil Nejad Sani Banaei Aysun, Eshaghkhani Yeganeh, Golchehre Zahra, Keramatipour Mohamm |
Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma.
JAMA network open 2022 08 5 (8): e2225647. Chen Cheng, Song Nan, Dong Qian, Sun Xiaojun, Mulder Heather L, Easton John, Zhang Jinghui, Yasui Yutaka, Bhatia Smita, Armstrong Gregory T, Wang Hui, Ness Kirsten K, Hudson Melissa M, Robison Leslie L, Wang Zhaomi |
Variants of SLC2A10 may be Linked to Poor Response to Metformin. Journal of the Endocrine Society 2022 Aug 6 (8): bvac092. Paz-Pacheco Elizabeth, Nevado Jose B, Cutiongco-de la Paz Eva Maria C, Jasul Gabriel V, Aman Aimee Yvonne Criselle L, Ribaya Elizabeth Laurize A, Francisco Mark David G, Guanzon Ma Luz Vicenta V, Uyking-Naranjo May L, Añonuevo-Cruz Ma Cecille S, Maningat Maria Patricia Deanna D, Jaring Cristina V, Nacpil-Dominguez Paulette D, Pala-Mohamad Aniza B, Canto Abigail U, Quisumbing John Paul M, Lat Annabelle Marie M, Bernardo Diane Carla C, Mansibang Noemie Marie M, Calpito Karell Jo Angelique C, Ribaya Vincent Sean D, Ferrer Julius Patrick Y, Biwang Jessica H, Melegrito Jodelyn B, Deguit Christian Deo T, Panerio Carlos Emmanuel |
STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency.
Frontiers in genetics 2022 1 12 736235. Lim Che Kang, Bronson Paola G, Varade Jezabel, Behrens Timothy W, Hammarström Lenna |
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 |
Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients. Psychopharmacology 2023 11 . Kosma Sakrajda, Karolina Bilska, Piotr M Czerski, Beata Naro?na, Monika Dmitrzak-W?glarz, Stefanie Heilmann-Heimbach, Felix F Brockschmidt, Stefan Herms, Markus M Nöthen, Sven Cichon, Barbara Wi?ckowska, Janusz K Rybakowski, Joanna Pawlak, Aleksandra Szczepankiewi |
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- Page last updated:Apr 22, 2024
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