Sarah B. Emery - Concepedia

Author

Sarah B. Emery

Also Known As

Alissa M. D’Gama, Changuk Chung, David W. Craig, Emery, Sarah, Emery, Sarah B., Huira C. Kopera, Ryan E. Mills, Ryan Mills, Sara Bizzotto, Sarah B Emery

Publications

44K

Citations

H-Index

Concepts

All Affiliations

University of Michigan Michigan Medicine Université de Rennes Centre National de la Recherche Scientifique Institut de génétique et de développement de Rennes

About

Sarah B. Emery is an author at University of Michigan specializing in medicine, genetics, and evolutionary biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	913
2	Natural Sciences	2	2	287
3	Biology	2	2	287
4	Public Health	1	1	54
5	Social Sciences	1	1	317

Sarah B. Emery

Publications

4.8K

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
A global reference for human genetic variation Adam Auton, Gonçalo R. Abecasis, David Altshuler, Civil War Book Review	2015	612
Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice Jérôme Ruel, Sarah B. Emery, Régis Nouvian, The American Journal of Human Genetics Knockout MouseNull MiceMolecular NeuroscienceMolecular PhysiologyDegenerative Disease	2008	317
The genomic landscape of polymorphic human nuclear mitochondrial insertions Gargi Dayama, Sarah B. Emery, Jeffrey M. Kidd, Nucleic Acids Research DnaGeneticsStatic Reference GenomesMolecular BiologyGenomics	2014	270
Comparison of village dog and wolf genomes highlights the role of the neural crest in dog domestication Amanda L. Pendleton, Feichen Shen, Angela M. Taravella Oill, BMC Biology	2018	169
Increased activity of <i>Diaphanous homolog 3</i> ( <i>DIAPH3</i> )/ <i>diaphanous</i> causes hearing defects in humans with auditory neuropathy and in <i>Drosophila</i> Cynthia J. Schoen, Sarah B. Emery, Marc C. Thorne, Proceedings of the National Academy of Sciences	2010	122
Identification of p.A684V missense mutation in the <i>WFS1</i> gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment Nanna Dahl Rendtorff, Marianne Lodahl, Houda Boulahbel, American Journal of Medical Genetics Part A Optic Atrophy-1 GeneMendelian DisorderGenetic DisorderGeneticsP.a684v Missense Mutation	2011	119
Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology Weichen Zhou, Sarah B. Emery, Diane A. Flasch, Nucleic Acids Research	2019	105
A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome Mark J. Rieder, Glenn E. Green, Sarah S. Park, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderHuman Homeotic TransformationGenetic Disorder	2012	96
Long-read assembly of a Great Dane genome highlights the contribution of GC-rich sequence and mobile elements to canine genomes Julia V. Halo, Amanda L. Pendleton, Feichen Shen, Proceedings of the National Academy of Sciences	2021	61

Page 1