Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and DAAM2[original query] |
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| DAAM2 polymorphism is closely related to the clinical outcomes of allogeneic hematopoietic stem cell transplantation. Annals of hematology 2012 Apr 91 (4): 571-6. Yi Hyeon Gyu, Piao Cheng Zhe, Kim Inho, Kim Hye Jin, Oh So Yeon, Kim Jin Won, Kim Dae-Young, Lim Joo Han, Seo Myung-Deok, Park Eunkyung, Yoon Sung-Soo, Kim Byoung Kook, Kim Chul Soo, Park Seonya |
| Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2018 Jul . Liu Yanhong, Lusk Christine M, Cho Michael H, Silverman Edwin K, Qiao Dandi, Zhang Ruyang, Scheurer Michael E, Kheradmand Farrah, Wheeler David A, Tsavachidis Spiridon, Armstrong Georgina, Zhu Dakai, Wistuba Ignacio I, Chow Chi-Wan B, Behrens Carmen, Pikielny Claudio W, Neslund-Dudas Christine, Pinney Susan M, Anderson Marshall, Kupert Elena, Bailey-Wilson Joan, Gaba Colette, Mandal Diptasri, You Ming, de Andrade Mariza, Yang Ping, Field John K, Liloglou Triantafillos, Davies Michael, Lissowska Jolanta, Swiatkowska Beata, Zaridze David, Mukeriya Anush, Janout Vladimir, Holcatova Ivana, Mates Dana, Milosavljevic Sasa, Scelo Ghislaine, Brennan Paul, McKay James, Liu Geoffrey, Hung Rayjean J, Christiani David C, Schwartz Ann G, Amos Christopher I, Spitz Margaret |
An atlas of genetic influences on osteoporosis in humans and mice.
Nature genetics 2019 02 51 (2): 258-266. Morris John A, Kemp John P, Youlten Scott E, Laurent Laetitia, Logan John G, Chai Ryan C, Vulpescu Nicholas A, Forgetta Vincenzo, Kleinman Aaron, Mohanty Sindhu T, Sergio C Marcelo, Quinn Julian, Nguyen-Yamamoto Loan, Luco Aimee-Lee, Vijay Jinchu, Simon Marie-Michelle, Pramatarova Albena, Medina-Gomez Carolina, Trajanoska Katerina, Ghirardello Elena J, Butterfield Natalie C, Curry Katharine F, Leitch Victoria D, Sparkes Penny C, Adoum Anne-Tounsia, Mannan Naila S, Komla-Ebri Davide S K, Pollard Andrea S, Dewhurst Hannah F, Hassall Thomas A D, Beltejar Michael-John G, , Adams Douglas J, Vaillancourt Suzanne M, Kaptoge Stephen, Baldock Paul, Cooper Cyrus, Reeve Jonathan, Ntzani Evangelia E, Evangelou Evangelos, Ohlsson Claes, Karasik David, Rivadeneira Fernando, Kiel Douglas P, Tobias Jonathan H, Gregson Celia L, Harvey Nicholas C, Grundberg Elin, Goltzman David, Adams David J, Lelliott Christopher J, Hinds David A, Ackert-Bicknell Cheryl L, Hsu Yi-Hsiang, Maurano Matthew T, Croucher Peter I, Williams Graham R, Bassett J H Duncan, Evans David M, Richards J Bre |
| Reanalysis of Exome Sequencing Data in the Indian Undiagnosed Diseases Program: Improving Diagnostic Yield and Ending Diagnostic Odyssey. Clinical genetics 2025 1 . Neha Garg, Pragna Lakshmi, Suzena M Singh, Samarth Kulshreshta, Prajnya Ranganath, Amita Moirangthem, Ashwin Dalal, Aakanksha Gahlot, Ratna Dua Pu |
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