Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

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From GWAS Catalog

The Catalog is a quality controlled, manually curated, literature-derived collection of all published genome-wide association studies.

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• Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.  
  Genome medicine 2017 Mar 9 (1): 23.
  Nagy Reka, Boutin Thibaud S, Marten Jonathan, Huffman Jennifer E, Kerr Shona M, Campbell Archie, Evenden Louise, Gibson Jude, Amador Carmen, Howard David M, Navarro Pau, Morris Andrew, Deary Ian J, Hocking Lynne J, Padmanabhan Sandosh, Smith Blair H, Joshi Peter, Wilson James F, Hastie Nicholas D, Wright Alan F, McIntosh Andrew M, Porteous David J, Haley Chris S, Vitart Veronique, Hayward Caroli
• Identification of unique venous thromboembolism-susceptibility variants in African-Americans.  
  Thrombosis and haemostasis 2017 Feb .
  Heit John A, Armasu Sebastian M, McCauley Bryan M, Kullo Iftikhar J, Sicotte Hugues, Pathak Jyotishman, Chute Christopher G, Gottesman Omri, Bottinger Erwin P, Denny Joshua C, Roden Dan M, Li Rongling, Ritchie Marylyn D, de Andrade Mari
• A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records. 
  PLoS genetics 2016 Oct 12 (10): e1006371.
  Hoffmann Thomas J, Keats Bronya J, Yoshikawa Noriko, Schaefer Catherine, Risch Neil, Lustig Lawrence
• Identification of Four Novel Loci in Asthma in European and African American Populations.  
  American journal of respiratory and critical care medicine 2016 Sep .
  Almoguera Berta, Vazquez Lyam, Mentch Frank, Connolly John, Pacheco Jennifer A, Sundaresan Agnes S, Peissig Peggy L, Linneman James G, McCarty Catherine A, Crosslin David, Carrell David S, Lingren Todd, Namjou-Khales Bahram, Harley John B, Larson Eric, Jarvik Gail P, Brilliant Murray, Williams Marc S, Kullo Iftikhar J, Hysinger Erik B, Sleiman Patrick M A, Hakonarson Hak
• A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.  
  The pharmacogenomics journal 2016 06 16 (3): 231-7.
  Mosley J D, Shaffer C M, Van Driest S L, Weeke P E, Wells Q S, Karnes J H, Velez Edwards D R, Wei W-Q, Teixeira P L, Bastarache L, Crawford D C, Li R, Manolio T A, Bottinger E P, McCarty C A, Linneman J G, Brilliant M H, Pacheco J A, Thompson W, Chisholm R L, Jarvik G P, Crosslin D R, Carrell D S, Baldwin E, Ralston J, Larson E B, Grafton J, Scrol A, Jouni H, Kullo I J, Tromp G, Borthwick K M, Kuivaniemi H, Carey D J, Ritchie M D, Bradford Y, Verma S S, Chute C G, Veluchamy A, Siddiqui M K, Palmer C N A, Doney A, MahmoudPour S H, Maitland-van der Zee A H, Morris A D, Denny J C, Roden D

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