Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: MYO16[original query] |
---|
An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes. Kidney international 2011 Jul 80 (1): 105-11. Pezzolesi Marcus G, Poznik G David, Skupien Jan, Smiles Adam M, Mychaleckyj Josyf C, Rich Stephen S, Warram James H, Krolewski Andrzej |
Fine mapping on chromosome 13q32-34 and brain expression analysis implicates MYO16 in schizophrenia. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2014 Mar 39 (4): 934-43. Rodriguez-Murillo Laura, Xu Bin, Roos J Louw, Abecasis Gonçalo R, Gogos Joseph A, Karayiorgou Mar |
Sex-specific association of a common variant of the XG gene with autism spectrum disorders. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Oct 162B (7): 742-50. Chang Shun-Chiao, Pauls David L, Lange Christoph, Sasanfar Roksana, Santangelo Susan |
Gene-education interactions identify novel blood pressure loci in the Framingham Heart Study. American journal of hypertension 2014 Mar 27 (3): 431-44. Basson Jacob, Sung Yun Ju, Schwander Karen, Kume Rezart, Simino Jeannette, de las Fuentes Lisa, Rao Dabee |
Identification of an interaction between VWF rs7965413 and platelet count as a novel risk marker for metabolic syndrome: an extensive search of candidate polymorphisms in a case-control study. PloS one 2015 10 (2): e0117591. Nakatochi Masahiro, Ushida Yasunori, Yasuda Yoshinari, Yoshida Yasuko, Kawai Shun, Kato Ryuji, Nakashima Toru, Iwata Masamitsu, Kuwatsuka Yachiyo, Ando Masahiko, Hamajima Nobuyuki, Kondo Takaaki, Oda Hiroaki, Hayashi Mutsuharu, Kato Sawako, Yamaguchi Makoto, Maruyama Shoichi, Matsuo Seiichi, Honda Hiroyu |
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. PLoS genetics 2021 Jul 17 (7): e1009679. Audain Enrique, Wilsdon Anna, Breckpot Jeroen, Izarzugaza Jose M G, Fitzgerald Tomas W, Kahlert Anne-Karin, Sifrim Alejandro, Wünnemann Florian, Perez-Riverol Yasset, Abdul-Khaliq Hashim, Bak Mads, Bassett Anne S, Benson D Woodrow, Berger Felix, Daehnert Ingo, Devriendt Koenraad, Dittrich Sven, Daubeney Piers Ef, Garg Vidu, Hackmann Karl, Hoff Kirstin, Hofmann Philipp, Dombrowsky Gregor, Pickardt Thomas, Bauer Ulrike, Keavney Bernard D, Klaassen Sabine, Kramer Hans-Heiner, Marshall Christian R, Milewicz Dianna M, Lemaire Scott, Coselli Joseph S, Mitchell Michael E, Tomita-Mitchell Aoy, Prakash Siddharth K, Stamm Karl, Stewart Alexandre F R, Silversides Candice K, Siebert Reiner, Stiller Brigitte, Rosenfeld Jill A, Vater Inga, Postma Alex V, Caliebe Almuth, Brook J David, Andelfinger Gregor, Hurles Matthew E, Thienpont Bernard, Larsen Lars Allan, Hitz Marc-Phill |
Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families. Current issues in molecular biology 2021 12 43 (3): 1778-1793. Fazia Teresa, Marzanati Daria, Carotenuto Anna Laura, Beecham Ashley, Hadjixenofontos Athena, McCauley Jacob L, Saddi Valeria, Piras Marialuisa, Bernardinelli Luisa, Gentilini Davi |
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus.
Human molecular genetics 2021 Dec . Suetsugu Hiroyuki, Kim Kwangwoo, Yamamoto Takuaki, Bang So-Young, Sakamoto Yuma, Shin Jung-Min, Sugano Nobuhiko, Kim Ji Soong, Mukai Masaya, Lee Yeon-Kyung, Ohmura Koichiro, Park Dae Jin, Takahashi Daisuke, Ahn Ga-Young, Karino Kohei, Kwon Young-Chang, Miyamura Tomoya, Kim Jihye, Nakamura Junichi, Motomura Goro, Kuroda Takeshi, Niiro Hiroaki, Miyamoto Takeshi, Takeuchi Tsutomu, Ikari Katsunori, Amano Koichi, Tada Yoshifumi, Yamaji Ken, Shimizu Masato, Atsumi Takashi, Seki Taisuke, Tanaka Yoshiya, Kubo Toshikazu, Hisada Ryo, Yoshioka Tomokazu, Yamazaki Mihoko, Kabata Tamon, Kajino Tomomichi, Ohta Yoichi, Okawa Takahiro, Naito Yohei, Kaneuji Ayumi, Yasunaga Yuji, Ohzono Kenji, Tomizuka Kohei, Koido Masaru, Matsuda Koichi, Okada Yukinori, Suzuki Akari, Kim Bong-Jo, Kochi Yuta, Lee Hye-Soon, Ikegawa Shiro, Bae Sang-Cheol, Terao Chikas |
Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka. BMC research notes 2022 Jun 15 (1): 190. Wijesiriwardhana Prabhavi, Musolf Anthony M, Bailey-Wilson Joan E, Wetthasinghe T Kalum, Dissanayake Vajira H |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: