Ryan E. Mills - Concepedia

Author

Ryan E. Mills

Also Known As

1000 Genomes Project, Alan P Boyle, Caleb A. Lareau, Charles Lee, Jeffrey M. Kidd, Kenneth Kwan, Kenneth Y. Kwan, Mallory Romanovitch, Mills, Ryan, Mills, Ryan E.

184

Publications

40K

Citations

H-Index

104

Concepts

All Affiliations

University of Michigan Harvard University Brigham and Women's Hospital Broad Institute University of Maryland, Baltimore

About

Ryan E. Mills is an author at University of Michigan specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	30	6.2K
2	Natural Sciences	14	14	2.2K
3	Engineering	5	5	1.1K
4	Public Health	4	4	1.3K
5	Health Sciences	1	1	46

Ryan E. Mills

Publications

13.3K

Citations

H-Index

Page 1

	Year	Citations
An integrated map of structural variation in 2,504 human genomes Peter H. Sudmant, Tobias Rausch, Eugene J. Gardner, Nature	2015	2.6K
Multi-platform discovery of haplotype-resolved structural variation in human genomes Mark Chaisson, Ashley D. Sanders, Xuefang Zhao, Nature Communications	2019	983
Haplotype-resolved diverse human genomes and integrated analysis of structural variation Peter Ebert, Peter A. Audano, Qihui Zhu, Science Structural VariationGeneticsMolecular BiologyGenomicsHuman Phenotypes	2021	753
An initial map of insertion and deletion (INDEL) variation in the human genome Ryan E. Mills, Christopher T. Luttig, Christine E. Larkins, Genome Research GeneticsHuman PolymorphismInitial MapMolecular GeneticsGenomics	2006	690
A global reference for human genetic variation Adam Auton, Gonçalo R. Abecasis, David Altshuler, Civil War Book Review	2015	612
Natural Mutagenesis of Human Genomes by Endogenous Retrotransposons Rebecca C. Iskow, Michael T. McCabe, Ryan E. Mills, Cell Natural MutagenesisGeneticsGenomic MechanismMolecular GeneticsMedicine	2010	557
A map of human genome variation from population-scale sequencing Richard Durbin, David L. Altshuler, Gonçalo R. Abecasis, HAL (Le Centre pour la Communication Scientifique Directe)	2010	542
CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome Peter K. Todd, Seok Yoon Oh, Amy Krans, Neuron Neurodegenerative DiseasesNeurological ProgressFragile X SpectrumDegenerative DiseaseNeuroscience	2013	478
A robust benchmark for detection of germline large deletions and insertions Justin M. Zook, Nancy F. Hansen, Nathan D. Olson, Nature Biotechnology EngineeringData ScienceData MiningGermline Large DeletionsComputational Biology	2020	460
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel Olivier Delaneau, Jonathan Marchini, Gil McVean, Nature Communications Haplotype DeterminationNext-generation SequencingGeneticsGenomes ProjectArray Data	2014	441

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