Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: ACP2[original query] |
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Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. American journal of human genetics 2007 Apr 80 (4): 769-78. Melquist Stacey, Craig David W, Huentelman Matthew J, Crook Richard, Pearson John V, Baker Matt, Zismann Victoria L, Gass Jennifer, Adamson Jennifer, Szelinger Szabolcs, Corneveaux Jason, Cannon Ashley, Coon Keith D, Lincoln Sarah, Adler Charles, Tuite Paul, Calne Donald B, Bigio Eileen H, Uitti Ryan J, Wszolek Zbigniew K, Golbe Lawrence I, Caselli Richard J, Graff-Radford Neill, Litvan Irene, Farrer Matthew J, Dickson Dennis W, Hutton Mike, Stephan Dietrich |
Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular genetics 2014 Jun 7 (3): 374-82. Cornes Belinda K, Brody Jennifer A, Nikpoor Naghmeh, Morrison Alanna C, Dang Huan Chu Pham, Ahn Byung Soo, Wang Shuai, Dauriz Marco, Barzilay Joshua I, Dupuis Josée, Florez Jose C, Coresh Josef, Gibbs Richard A, Kao W H Linda, Liu Ching-Ti, McKnight Barbara, Muzny Donna, Pankow James S, Reid Jeffrey G, White Charles C, Johnson Andrew D, Wong Tien Y, Psaty Bruce M, Boerwinkle Eric, Rotter Jerome I, Siscovick David S, Sladek Robert, Meigs James |
A genome-wide association study of corneal astigmatism: The CREAM Consortium.
Molecular vision 2018 24 127-142. Shah Rupal L, Li Qing, Zhao Wanting, Tedja Milly S, Tideman J Willem L, Khawaja Anthony P, Fan Qiao, Yazar Seyhan, Williams Katie M, Verhoeven Virginie J M, Xie Jing, Wang Ya Xing, Hess Moritz, Nickels Stefan, Lackner Karl J, Pärssinen Olavi, Wedenoja Juho, Biino Ginevra, Concas Maria Pina, Uitterlinden André, Rivadeneira Fernando, Jaddoe Vincent W V, Hysi Pirro G, Sim Xueling, Tan Nicholas, Tham Yih-Chung, Sensaki Sonoko, Hofman Albert, Vingerling Johannes R, Jonas Jost B, Mitchell Paul, Hammond Christopher J, Höhn René, Baird Paul N, Wong Tien-Yin, Cheng Chinfsg-Yu, Teo Yik Ying, Mackey David A, Williams Cathy, Saw Seang-Mei, Klaver Caroline C W, Guggenheim Jeremy A, Bailey-Wilson Joan E, |
Genetic diversity and functional effect of common polymorphisms in genes involved in the first heterodimeric complex of the Nucleotide Excision Repair pathway. DNA repair 2019 Dec 86 102770. Hamdi Yosr, Jerbi Manel, Romdhane Lilia, Ben Rekaya Mariem, El Benna Houda, Chouchane Lotfi, Boubaker Mohamed Samir, Abdelhak Sonia, Yacoub-Youssef Hou |
Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis.
Neurology(R) neuroimmunology & neuroinflammation 2021 Nov 8 (6): . Tietz Anja K, Angstwurm Klemens, Baumgartner Tobias, Doppler Kathrin, Eisenhut Katharina, Elisak Martin, Franke Andre, Golombeck Kristin S, Handreka Robert, Kaufmann Max, Kraemer Markus, Kraft Andrea, Lewerenz Jan, Lieb Wolfgang, Madlener Marie, Melzer Nico, Mojzisova Hana, Möller Peter, Pfefferkorn Thomas, Prüss Harald, Rostásy Kevin, Schnegelsberg Margret, Schröder Ina, Siebenbrodt Kai, Sühs Kurt-Wolfram, Wickel Jonathan, Wandinger Klaus-Peter, Leypoldt Frank, Kuhlenbäumer Gregor, |
Co-existence of multiple functional variants and genes underlie genetic risk locus 11p11.2 of Alzheimer's disease. Biological psychiatry 2023 6 . Min Xu, Qianjin Liu, Rui Bi, Yu Li, Hongli Li, Wei-Bo Kang, Zhongjiang Yan, Quanzhen Zheng, Chunli Sun, Maosen Ye, Bo-Lin Xiang, Xiong-Jian Luo, Ming Li, Deng-Feng Zhang, Yong-Gang Y |
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