Christopher W. Whelan

Author

Also Known As

Byrnes, Andrea, C Whelan, Christopher W Whelan, Christopher W. Whelan, Christopher Whelan, Mark Walker, Nicholas A. Watts, Whelan, Christopher, Whelan, Christopher W.

Publications

3.2K

Citations

H-Index

Concepts

All Affiliations

Broad Institute Harvard University Massachusetts General Hospital University of Bari Aldo Moro Oregon Health & Science University

About

Christopher W. Whelan is an author at Broad Institute specializing in genetics, medicine, and systems biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	947
2	Education	1	1	50
3	Engineering	1	1	12
4	Public Health	1	1	113
5	Biology	1	1	12

Christopher W. Whelan

Publications

3.1K

Citations

H-Index

Page 1

	Year	Citations
A structural variation reference for medical and population genetics Ryan L. Collins, Harrison Brand, Konrad J. Karczewski, Nature	2020	1.1K
Gibbon genome and the fast karyotype evolution of small apes Lucia Carbone, R. Alan Harris, Sante Gnerre, Nature	2014	388
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing Srinivas R. Viswanathan, Gavin Ha, Andreas Hoff, Cell Long-read SequencingLinked-read Genome SequencingUrologyFunctional GenomicsNext-generation Sequencing	2018	368
Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice Melis Yilmaz, Esra Yalçın, Jessy Présumey, Nature Neuroscience	2020	314
Complement genes contribute sex-biased vulnerability in diverse disorders Nolan Kamitaki, Aswin Sekar, Robert E. Handsaker, Nature Complement SystemGenetic DisorderGeneticsImmunologyHost Genetics	2020	253
GATK PathSeq: a customizable computational tool for the discovery and identification of microbial sequences in libraries from eukaryotic hosts Mark Walker, Chandra Sekhar Pedamallu, Akinyemi I. Ojesina, Bioinformatics	2018	128
A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica Karol Estrada, Christopher W. Whelan, Fengmei Zhao, Nature Communications	2018	122
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population Andrea Ganna, Giulio Genovese, Daniel P. Howrigan, Nature Neuroscience Genetic TestingGenetic DisorderDamaging MutationsGeneticsMedicine	2016	113
Genomic organization and evolution of double minutes/homogeneously staining regions with<i>MYC</i>amplification in human cancer Alberto L’Abbate, Gemma Macchia, Pietro D’Addabbo, Nucleic Acids Research GeneticsMolecular BiologyGenomicsCancer BiologyEpigenetics	2014	108
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies Chelsea Lowther, Elise Valkanas, Jessica L. Giordano, The American Journal of Human Genetics Autistic WomanMedicineGeneticsNext-generation SequencingPediatrics	2023	50

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