Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: VPS13B[original query] |
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Genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2010 Apr 21 (4): 579-87. Deng F-Y, Zhao L-J, Pei Y-F, Sha B-Y, Liu X-G, Yan H, Wang L, Yang T-L, Recker R R, Papasian C J, Deng H |
Frameshift mutations of vacuolar protein sorting genes in gastric and colorectal cancers with microsatellite instability. Human pathology 2012 Jan 43 (1): 40-7. An Chang Hyeok, Kim Yoo Ri, Kim Ho Shik, Kim Sung Soo, Yoo Nam Jin, Lee Sug Hyu |
Using whole-exome sequencing to identify inherited causes of autism. Neuron 2013 Jan 77 (2): 2. Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, Leclair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA |
Whole Exome Sequencing Identifies a Novel Homozygous Duplication Mutation in the VPS13B Gene in an Indian Family with Cohen Syndrome. Journal of molecular neuroscience : MN 2020 3 70 (8): 1225-1228. Kaushik Pankhuri, Mahajan Naresh, Girimaji Satish C, Kumar Ar |
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Scientific reports 2020 Feb 10 (1): 3198. Bacchelli Elena, Cameli Cinzia, Viggiano Marta, Igliozzi Roberta, Mancini Alice, Tancredi Raffaella, Battaglia Agatino, Maestrini Ele |
Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort. Genes 2021 5 12 (5): . Kim Yoon-Jeon, Kim You-Na, Yoon Young-Hee, Seo Eul-Ju, Seo Go-Hun, Keum Changwon, Lee Beom-Hee, Lee Joo-Yo |
Genomic Analysis of Korean Patient With Microcephaly. Frontiers in genetics 2021 2 11 543528. Lee Jiwon, Park Jong Eun, Lee Chung, Kim Ah Reum, Kim Byung Joon, Park Woong-Yang, Ki Chang-Seok, Lee Jeeh |
A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.
Journal of genetics and genomics = Yi chuan xue bao 2021 2 48 (3): 198-207. Huang Yin, Li Dan, Qiao Lu, Liu Yu, Peng Qianqian, Wu Sijie, Zhang Manfei, Yang Yajun, Tan Jingze, Xu Shuhua, Jin Li, Wang Sijia, Tang Kun, Grünewald Stef |
A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.
Science advances 2021 2 7 (6): . Bonfante Betty, Faux Pierre, Navarro Nicolas, Mendoza-Revilla Javier, Dubied Morgane, Montillot Charlotte, Wentworth Emma, Poloni Lauriane, Varón-González Ceferino, Jones Philip, Xiong Ziyi, Fuentes-Guajardo Macarena, Palmal Sagnik, Chacón-Duque Juan Camilo, Hurtado Malena, Villegas Valeria, Granja Vanessa, Jaramillo Claudia, Arias William, Barquera Rodrigo, Everardo-Martínez Paola, Sánchez-Quinto Mirsha, Gómez-Valdés Jorge, Villamil-Ramírez Hugo, Silva de Cerqueira Caio C, Hünemeier Tábita, Ramallo Virginia, Liu Fan, Weinberg Seth M, Shaffer John R, Stergiakouli Evie, Howe Laurence J, Hysi Pirro G, Spector Timothy D, Gonzalez-José Rolando, Schüler-Faccini Lavinia, Bortolini Maria-Cátira, Acuña-Alonzo Victor, Canizales-Quinteros Samuel, Gallo Carla, Poletti Giovanni, Bedoya Gabriel, Rothhammer Francisco, Thauvin-Robinet Christel, Faivre Laurence, Costedoat Caroline, Balding David, Cox Timothy, Kayser Manfred, Duplomb Laurence, Yalcin Binnaz, Cotney Justin, Adhikari Kaustubh, Ruiz-Linares Andr |
Quantitative trait locus analysis for endophenotypes reveals genetic substrates of core symptom domains and neurocognitive function in autism spectrum disorder. Translational psychiatry 2022 9 12 (1): 407. Lee In-Hee, Koelliker Ekaterina, Kong Sek W |
Multiple genetic variants involved in both autoimmunity and autoinflammation detected in Chinese patients with sporadic Meniere's disease: a preliminary study. Frontiers in neurology 2023 6 14 1159658. Jing Zou, Guoping Zhang, Hongbin Li, Zikai Zhao, Qing Zhang, Ilmari Pyykkö, Antti Mäkit |
Multiplex allele-specific polymerase chain reaction-based prevalence study of canine trapped neutrophil syndrome in Thailand. Veterinary world 2023 12 16 (11): 2271-2276. Chommanad Lerdkrai, Nuch Phungphos |
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- Page last updated:Apr 29, 2024
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