Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and IMMP2L[original query] |
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| Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study. Current Alzheimer research 2012 Sep 9 (7): 801-14. Swaminathan Shanker, Shen Li, Kim Sungeun, Inlow Mark, West John D, Faber Kelley M, Foroud Tatiana, Mayeux Richard, Saykin Andrew J, , |
| Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome. European journal of human genetics : EJHG 2014 Nov 22 (11): 1283-9. Bertelsen Birgitte, Melchior Linea, Jensen Lars R, Groth Camilla, Glenthøj Birte, Rizzo Renata, Debes Nanette Mol, Skov Liselotte, Brøndum-Nielsen Karen, Paschou Peristera, Silahtaroglu Asli, Tümer Zeyn |
| Genetic associations for keratoconus: a systematic review and meta-analysis. Scientific reports 2017 Jul 7 (1): 4620. Rong Shi Song, Ma Sarah Tsz Ue, Yu Xin Ting, Ma Li, Chu Wai Kit, Chan Tommy Chung Yan, Wang Yu Meng, Young Alvin L, Pang Chi Pui, Jhanji Vishal, Chen Li J |
| Replication of SNP associations with keratoconus in a Czech cohort. PloS one 2017 12 (2): e0172365. Liskova Petra, Dudakova Lubica, Krepelova Anna, Klema Jiri, Hysi Pirro |
| Genome-wide copy number variation association study in anorexia nervosa. Molecular psychiatry 2024 11 . Alicia Walker, Robert Karlsson, Jin P Szatkiewicz, Laura M Thornton, Zeynep Yilmaz, Virpi M Leppä, Androula Savva, Tian Lin, Julia Sidorenko, Allan McRae, George Kirov, Helena L Davies, Bengt T Fundín, Samuel J R A Chawner, Jie Song, Stina Borg, Jia Wen, Hunna J Watson, Melissa A Munn-Chernoff, Jessica H Baker, Scott Gordon, Wade H Berrettini, Harry Brandt, Steven Crawford, Katherine A Halmi, Allan S Kaplan, Walter H Kaye, James Mitchell, Michael Strober, D Blake Woodside, Nancy L Pedersen, Richard Parker, Jennifer Jordan, Martin A Kennedy, Andreas Birgegård, Mikael Landén, Nicholas G Martin, Patrick F Sullivan, Cynthia M Bulik, Naomi R Wr |
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