Author details

Full Name

Adam Kiezun

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
30718883	Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes.	Eur J Hum Genet	2019
28854867	An Embryonic and Induced Pluripotent Stem Cell Model for Ovarian Granulosa Cell Development and Steroidogenesis.	Reprod Sci	2018
29051179	Analysis of <i>ITGB2</i> rare germ line variants in chronic lymphocytic leukemia.	Blood	2017
28652578	Rare germline variants in ATM are associated with chronic lymphocytic leukemia.	Leukemia	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
25751620	Efficient differentiation of steroidogenic and germ-like cells from epigenetically-related iPSCs derived from ovarian granulosa cells.	PLoS One	2015
25487149	Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.	Nature	2015
26638776	Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution.	Nat Commun	2015
24836576	Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.	Nat Med	2014
25512523	Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma.	Proc Natl Acad Sci U S A	2014
24909177	Exome sequencing of pleuropulmonary blastoma reveals frequent biallelic loss of TP53 and two hits in DICER1 resulting in retention of 5p-derived miRNA hairpin loop sequences.	Oncogene	2014
25186949	The genomic landscape of pediatric Ewing sarcoma.	Cancer Discov	2014
23334666	The genetic landscape of high-risk neuroblastoma.	Nat Genet	2013
23861739	Fine-scale patterns of population stratification confound rare variant association tests.	PLoS One	2013
23770567	Mutational heterogeneity in cancer and the search for new cancer-associated genes.	Nature	2013
23852170	An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers.	Nat Genet	2013
24185511	Somatic mutation of CDKN1B in small intestine neuroendocrine tumors.	Nat Genet	2013
23468643	Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency.	PLoS Genet	2013
23060611	Network-based inference from complex proteomic mixtures using SNIPE.	Bioinformatics	2012
22641211	Exome sequencing and the genetic basis of complex traits.	Nat Genet	2012
22330228	miRviewer: a multispecies microRNA homologous viewer.	BMC Research Notes	2012
21993625	Genome sequencing reveals insights into physiology and longevity of the naked mole rat.	Nature	2011
21310275	Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.	Am J Hum Genet	2011
21920052	Computational and statistical approaches to analyzing variants identified by exome sequencing.	Genome Biol	2011
19293999	Evaluation of optimization techniques for variable selection in logistic regression applied to diagnosis of myocardial infarction.		2009
18215311	miRNAminer: a tool for homologous microRNA gene search.	BMC Bioinformatics	2008