| Genetic IL-6 Signaling Deficiency Attenuates Cardiovascular Risk in Clonal Hematopoiesis AG Bick, JP Pirruccello, GK Griffin, N Gupta, S Gabriel, D Saleheen, ... Circulation, 2019 | | 2019 |
| Correction: 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, 1-3, 2019 | | 2019 |
| Harmonizing Clinical Sequencing And Interpretation For The eMERGE III Network H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ... The American Journal of Human Genetics 105 (3), 588-605, 2019 | 1 | 2019 |
| Clinical whole genome sequencing at scale A MacBeth, T Bowers, B Woolf, M Harden, N Lennon, S Gabriel Cancer Research 79 (13 Supplement), 3543-3543, 2019 | | 2019 |
| Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls J Flannick, JM Mercader, C Fuchsberger, MS Udler, A Mahajan, J Wessel, ... Nature 570 (7759), 71-76, 2019 | 20 | 2019 |
| Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation NJ Abdulhay, C Fiorini, JM Verboon, LS Ludwig, JC Ulirsch, B Zieger, ... Journal of Experimental Medicine 216 (5), 1050-1060, 2019 | 3 | 2019 |
| Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia M Alver, M Palover, A Saar, K Läll, SM Zekavat, N Tõnisson, L Leitsalu, ... Genetics in Medicine 21 (5), 1173-1180, 2019 | 5 | 2019 |
| Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease JM Tilghman, AY Ling, TN Turner, MX Sosa, N Krumm, S Chatterjee, ... New England Journal of Medicine 380 (15), 1421-1432, 2019 | 14 | 2019 |
| Whole-genome sequencing to characterize monogenic and polygenic contributions in patients hospitalized with early-onset myocardial infarction AV Khera, M Chaffin, SM Zekavat, RL Collins, C Roselli, P Natarajan, ... Circulation 139 (13), 1593-1602, 2019 | 21 | 2019 |
| Employment Cost Index, Historical Listing–Volume V: Continuous Occupational and Industry Series: September 1975-December 2017. Table 4: employment cost index for total … EJ Benjamin, P Muntner, A Alonso, MS Bittencourt, CW Callaway, ... Circulation 139 (10), e56-e528, 2019 | | 2019 |
| 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 15 (3 …, 2019 | 6 | 2019 |
| Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease A Nomura, CA Emdin, HH Won, GM Peloso, P Natarajan, D Ardissino, ... BioRxiv, 780734, 2019 | | 2019 |
| Addendum: The Cancer Cell Line modelling of anticancer drug sensitivity CORRECTIONS & AMENDMENTS J Barretina, G Caponigro, N Stransky, K Venkatesan, AA Margolin, S Kim, ... Springer US, 2019 | | 2019 |
| The gastrointestinal development ‘parts list’: transcript profiling of embryonic gut development in wildtype and Ret-deficient mice S Chatterjee, P Nandakumar, DR Auer, SB Gabriel, A Chakravarti bioRxiv, 730010, 2019 | | 2019 |
| Use of> 100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in … MH Kowalski, H Qian, Z Hou, JD Rosen, AL Tapia, Y Shan, D Jain, ... bioRxiv, 683201, 2019 | | 2019 |
| A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease CA Emdin, M Haas, AV Khera, K Aragam, M Chaffin, L Jiang, WQ Wei, ... BioRxiv, 594523, 2019 | 1 | 2019 |
| Erratum: Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity (Nature (2012) 483 7391 (603-607)) J Barretina, G Caponigro, N Stransky, K Venkatesan, A Margolin, S Kim, ... Nature 565 (7738), 2019 | | 2019 |
| An open resource of structural variation for medical and population genetics RL Collins, H Brand, KJ Karczewski, X Zhao, J Alföldi, AV Khera, ... BioRxiv, 578674, 2019 | 6 | 2019 |
| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... BioRxiv, 563866, 2019 | 19 | 2019 |
| Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes KJ Karczewski, LC Francioli, G Tiao, BB Cummings, J Alföldi, Q Wang, ... BioRxiv, 531210, 2019 | 113 | 2019 |