Stacey Gabriel
Stacey Gabriel
The Broad Institute of Harvard and MIT
Verified email at broadinstitute.org
TitleCited byYear
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
12019
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
202019
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
32019
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
52019
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
142019
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
212019
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
62019
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
12019
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
62019
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
192019
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
1132019
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Articles 1–20