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| A robust benchmark for detection of germline large deletions and insertions JM Zook, NF Hansen, ND Olson, L Chapman, JC Mullikin, C Xiao, ... Nature biotechnology 38 (11), 1347-1355, 2020 | 340 | 2020 |
| Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ... Molecular psychiatry, 1, 2018 | 269 | 2018 |
| Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF‐β/BMP pathway VG Nolan, A Adewoye, C Baldwin, L Wang, Q Ma, DF Wyszynski, ... British journal of haematology 133 (5), 570-578, 2006 | 232 | 2006 |
| Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea Q Ma, DF Wyszynski, JJ Farrell, A Kutlar, LA Farrer, CT Baldwin, ... The pharmacogenomics journal 7 (6), 386-394, 2007 | 147 | 2007 |
| A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression JJ Farrell, RM Sherva, Z Chen, H Luo, BF Chu, SY Ha, CK Li, ACW Lee, ... Blood 117 (18), 4935-4945, 2011 | 144 | 2011 |
| A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression JJ Farrell, RM Sherva, Z Chen, H Luo, BF Chu, SY Ha, CK Li, ACW Lee, ... Blood 117 (18), 4935-4945, 2011 | 144 | 2011 |
| Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans MW Logue, M Schu, BN Vardarajan, J Farrell, DA Bennett, JD Buxbaum, ... Alzheimer's & Dementia 10 (6), 609-618. e11, 2014 | 129 | 2014 |
| Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis C Baldwin, VG Nolan, DF Wyszynski, QL Ma, P Sebastiani, SH Embury, ... Blood 106 (1), 372-375, 2005 | 122 | 2005 |
| Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis C Baldwin, VG Nolan, DF Wyszynski, QL Ma, P Sebastiani, SH Embury, ... Blood 106 (1), 372-375, 2005 | 122 | 2005 |
| Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemia VG Nolan, C Baldwin, Q Ma, DF Wyszynski, Y Amirault, JJ Farrell, ... British journal of haematology 128 (2), 266-272, 2005 | 94 | 2005 |
| Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype D Ngo, H Bae, MH Steinberg, P Sebastiani, N Solovieff, CT Baldwin, ... Blood Cells, Molecules, and Diseases, 2013 | 81 | 2013 |
| A search for age-related macular degeneration risk variants in Alzheimer disease genes and pathways MW Logue, M Schu, BN Vardarajan, J Farrell, KL Lunetta, G Jun, ... Neurobiology of Aging, 2013 | 72 | 2013 |
| Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry D Patel, J Mez, BN Vardarajan, L Staley, J Chung, X Zhang, JJ Farrell, ... JAMA network open 2 (3), e191350-e191350, 2019 | 64 | 2019 |
| APOE Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of APOE ε4 on Alzheimer’s Disease Risk in a Multiracial Sample KY Choi, JJ Lee, TI Gunasekaran, S Kang, W Lee, J Jeong, HJ Lim, ... Journal of clinical medicine 8 (8), 1236, 2019 | 60 | 2019 |
| BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia P Sebastiani, JJ Farrell, A Alsultan, S Wang, HL Edward, H Shappell, ... Blood Cells, Molecules, and Diseases 54 (3), 224-230, 2015 | 54 | 2015 |
| Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia. DF Wyszynski, CT Baldwin, MA Cleves, Y Amirault, VG Nolan, JJ Farrell, ... Cellular and molecular biology (Noisy-le-Grand, France) 50 (1), 23, 2004 | 53 | 2004 |
| Association of Polymorphisms of IGF1R and Genes in the Transforming Growth Factor–β/Bone Morphogenetic Protein Pathway with Bacteremia in Sickle Cell Anemia AH Adewoye, VG Nolan, Q Ma, C Baldwin, DF Wyszynski, JJ Farrell, ... Clinical infectious diseases 43 (5), 593-598, 2006 | 51 | 2006 |
| Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans I Akinsheye, N Solovieff, D Ngo, A Malek, P Sebastiani, MH Steinberg, ... American journal of hematology 87 (2), 217-219, 2012 | 50 | 2012 |
| A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease X Zhang, C Zhu, G Beecham, BN Vardarajan, Y Ma, D Lancour, JJ Farrell, ... Alzheimer's & dementia: the journal of the Alzheimer's Association, 2018 | 48 | 2018 |
