Detalhe da pesquisa
1.
A comprehensive analysis of clinical and polygenic germline influences on somatic mutational burden.
Am J Hum Genet
; 111(2): 242-258, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38211585
2.
Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations.
PLoS Genet
; 18(11): e1010447, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36342933
3.
Identifying causal variants by fine mapping across multiple studies.
PLoS Genet
; 17(9): e1009733, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34543273
4.
Ensemble neural network model for detecting thyroid eye disease using external photographs.
Br J Ophthalmol
; 107(11): 1722-1729, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36126104
5.
MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record.
medRxiv
; 2023 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37986972
6.
Ancestry-driven recalibration of tumor mutational burden and disparate clinical outcomes in response to immune checkpoint inhibitors.
Cancer Cell
; 40(10): 1161-1172.e5, 2022 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36179682
7.
Constructing germline research cohorts from the discarded reads of clinical tumor sequences.
Genome Med
; 13(1): 179, 2021 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34749793
8.
Technology dictates algorithms: recent developments in read alignment.
Genome Biol
; 22(1): 249, 2021 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34446078