PMC Links for Nucleotide (Select 1717508344) - PMC

Select item 54916931.

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

Jacqueline M. Lane, Jingjing Liang, Irma Vlasac, Simon G. Anderson, David A. Bechtold, Jack Bowden, Richard Emsley, Shubhroz Gill, Max A. Little, AnneMarie I. Luik, Andrew Loudon, Frank A.J.L. Scheer, Shaun M. Purcell, Simon D. Kyle, Deborah A. Lawlor, Xiaofeng Zhu, Susan Redline, David W. Ray, Martin K. Rutter, Richa Saxena

Nat Genet. Author manuscript; available in PMC 2017 Jun 30.

Published in final edited form as: Nat Genet. 2017 Feb; 49(2): 274–281. Published online 2016 Dec 19. doi: 10.1038/ng.3749

PMCID:: PMC5491693

Article PDF–1.3M

Select item 38637102.

Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: A genome-wide interaction study

Anja Rudolph, Rebecca Hein, Sara Lindström, Lars Beckmann, Sabine Behrens, Jianjun Liu, Hugues Aschard, Manjeet K. Bolla, Jean Wang, Thérèse Truong, Emilie Cordina-Duverger, Florence Menegaux, Thomas Brüning, Volker Harth, The GENICA Network, Gianluca Severi, Laura Baglietto, Melissa Southey, Stephen J. Chanock, Jolanta Lissowska, Jonine D. Figueroa, Mikael Eriksson, Keith Humpreys, Hatef Darabi, Janet E. Olson, Kristen N. Stevens, Celine M. Vachon, Julia A. Knight, Gord Glendon, Anna Marie Mulligan, Alan Ashworth, Nicholas Orr, Minouk Schoemaker, Penny M. Webb, kConFab Investigators, AOCS Management Group, Pascal Guénel, Hiltrud Brauch, Graham Giles, Montserrat García-Closas, Kamila Czene, Georgia Chenevix-Trench, Fergus J. Couch, Irene L. Andrulis, Anthony Swerdlow, David J. Hunter, Dieter Flesch-Janys, Douglas F. Easton, Per Hall, Heli Nevanlinna, Peter Kraft, Jenny Chang-Claude

Endocr Relat Cancer. Author manuscript; available in PMC 2014 Dec 1.

Published in final edited form as: Endocr Relat Cancer. 2013 Dec; 20(6): 875–887. Published online 2013 Nov 4. doi: 10.1530/ERC-13-0349

PMCID:: PMC3863710

Abstract Article PDF–505K

Select item 17352843.

Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region

H Kehrer-Sawatzki, S Tinschert, D Jenne

J Med Genet. 2003 Oct; 40(10): e116. doi: 10.1136/jmg.40.10.e116

PMCID:: PMC1735284

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