| It’s time to phase-in RHD genotyping for patients with a serological weak D phenotype SG Sandler, WA Flegel, CM Westhoff, GA Denomme, M Delaney, ... Transfusion 55 (3), 680, 2015 | 202 | 2015 |
| Differential expression of Fcγ RIIA, Fcγ RIIB and Fcγ RIIC in hematopoietic cells: analysis of transcripts DL Cassel, MA Keller, S Surrey, E Schwartz, AD Schreiber, EF Rappaport, ... Molecular immunology 30 (5), 451-460, 1993 | 162 | 1993 |
| International society of blood transfusion working party on red cell immunogenetics and blood group terminology: report of the Dubai, Copenhagen and Toronto meetings JR Storry, FB Clausen, L Castilho, Q Chen, G Daniels, G Denomme, ... Vox sanguinis 114 (1), 95-102, 2019 | 119 | 2019 |
| RH genotype matching for transfusion support in sickle cell disease ST Chou, P Evans, S Vege, SL Coleman, DF Friedman, M Keller, ... Blood, The Journal of the American Society of Hematology 132 (11), 1198-1207, 2018 | 111 | 2018 |
| International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetings JR Storry, L Castilho, Q Chen, G Daniels, G Denomme, WA Flegel, ... ISBT science series 11 (2), 118-122, 2016 | 106 | 2016 |
| Association of T‐786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease K Sharan, S Surrey, S Ballas, M Borowski, M Devoto, KF Wang, E Sandler, ... British journal of haematology 124 (2), 240-243, 2004 | 87 | 2004 |
| A soluble form of the human Fc receptor Fc gamma RIIA: cloning, transcript analysis and detection. EF Rappaport, DL Cassel, DO Walterhouse, SE McKenzie, S Surrey, ... Experimental hematology 21 (5), 689-696, 1993 | 73 | 1993 |
| Financial implications of RHD genotyping of pregnant women with a serologic weak D phenotype S Kacker, R Vassallo, MA Keller, CM Westhoff, KD Frick, SG Sandler, ... Transfusion 55 (9), 2095-2103, 2015 | 71 | 2015 |
| Erythroid-induced commitment of K562 cells results in clusters of differentially expressed genes enriched for specific transcription regulatory elements S Addya, MA Keller, K Delgrosso, CM Ponte, R Vadigepalli, GE Gonye, ... Physiological genomics 19 (1), 117-130, 2004 | 71 | 2004 |
| Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulators MA Keller, S Addya, R Vadigepalli, B Banini, K Delgrosso, H Huang, ... Physiological genomics 28 (1), 114-128, 2006 | 65 | 2006 |
| Coriell Personalized Medicine Collaborative®: a prospective study of the utility of personalized medicine MA Keller, ES Gordon, CB Stack, N Gharani, CJ Sill, TJ Schmidlen, ... Personalized Medicine 7 (3), 301-317, 2010 | 60 | 2010 |
| Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor ER Londin, MA Keller, MR D'Andrea, K Delgrosso, A Ertel, S Surrey, ... BMC genomics 12, 1-9, 2011 | 58 | 2011 |
| Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci JF Meschia, M Nalls, M Matarin, TG Brott, RD Brown Jr, J Hardy, B Kissela, ... Stroke 42 (10), 2726-2732, 2011 | 49 | 2011 |
| It's time to phase out “serologic weak D phenotype” and resolve D types with RHD genotyping including weak D type 4 WA Flegel, GA Denomme, JT Queenan, ST Johnson, MA Keller, ... Transfusion 60 (4), 855-859, 2020 | 47 | 2020 |
| Genetic knowledge among participants in the Coriell Personalized Medicine Collaborative TJ Schmidlen, L Scheinfeldt, R Zhaoyang, R Kasper, K Sweet, ES Gordon, ... Journal of genetic counseling 25, 385-394, 2016 | 44 | 2016 |
| The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system N Gharani, MA Keller, CB Stack, LM Hodges, TJ Schmidlen, DE Lynch, ... Genome medicine 5, 1-19, 2013 | 41 | 2013 |
| Genetic risk estimation in the coriell personalized medicine collaborative CB Stack, N Gharani, ES Gordon, T Schmidlen, MF Christman, MA Keller Genetics in Medicine 13 (2), 131-139, 2011 | 41 | 2011 |
| CoAIMs: a cost-effective panel of ancestry informative markers for determining continental origins ER Londin, MA Keller, C Maista, G Smith, LA Mamounas, R Zhang, ... PLoS One 5 (10), e13443, 2010 | 41 | 2010 |
| College of American Pathologists Transfusion Medicine Resource Committee Work Group. It’s time to phase in RHD genotyping for patients with a serologic weak D phenotype SG Sandler, WA Flegel, CM Westhoff, GA Denomme, M Delaney, ... Transfusion 55 (3), 680-9, 2015 | 29 | 2015 |
| Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery K Gwinn, RA Corriveau, H Mitsumoto, K Bednarz, RH Brown Jr, ... PloS one 2 (12), e1254, 2007 | 27 | 2007 |
