Author details

Full Name

Grace Tiao

Affiliation

ORCID

Career Start Year

2006

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36747613	A harmonized public resource of deeply sequenced diverse human genomes.	bioRxiv	2024
38057664	A genomic mutational constraint map using variation in 76,156 human genomes.	Nature	2024
38057443	Inferring compound heterozygosity from large-scale exome sequencing data.	Nat Genet	2024
36993580	Inferring compound heterozygosity from large-scale exome sequencing data.	bioRxiv	2023
37214979	Insights from a genome-wide truth set of tandem repeat variation.	bioRxiv	2023
36697832	Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.	Nature	2023
35074858	Mitochondrial DNA variation across 56,434 individuals in gnomAD.	Genome Res	2022
35396579	Rare coding variants in ten genes confer substantial risk for schizophrenia.	Nature	2022
34373650	Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2021
33536627	Author Correction: A structural variation reference for medical and population genetics.	Nature	2021
33536625	Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2021
32461654	The mutational constraint spectrum quantified from variation in 141,456 humans.	Nature	2020
30718883	Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes.	Eur J Hum Genet	2019
27707790	Landscape of Genomic Alterations in Pituitary Adenomas.	Clin Cancer Res	2017
28825726	A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer.	Nat Genet	2017
28658208	Recurrent and functional regulatory mutations in breast cancer.	Nature	2017
28652578	Rare germline variants in ATM are associated with chronic lymphocytic leukemia.	Leukemia	2017
29051179	Analysis of <i>ITGB2</i> rare germ line variants in chronic lymphocytic leukemia.	Blood	2017
27535533	Analysis of protein-coding genetic variation in 60,706 humans.	Nature	2016
26372948	Comprehensive analysis of cancer-associated somatic mutations in class I HLA genes.	Nat Biotechnol	2015
26638776	Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution.	Nat Commun	2015
22314356	Rapid microbial response to the presence of an ancient relic in the Antarctic Dry Valleys.	Nature Communications	2012
17229284	Insights into the gyrification of developing ferret brain by magnetic resonance imaging.	J Anat	2007
16320251	Overlapping expression of ARFGEF2 and Filamin A in the neuroependymal lining of the lateral ventricles: insights into the cause of periventricular heterotopia.	J Comp Neurol	2006