Kerry K. Brown - Concepedia

Concepedia

Author

Kerry K. Brown

Brigham and Women's Hospital

Also Known As

Brown, Kerry K., Kerry Brown, Kerry K Brown, Kerry K. Brown

18

Publications

3.2K

Citations

10

H-Index

52

Concepts

All Affiliations

Brigham and Women's Hospital Harvard University Mass General Brigham Boston Children's Hospital University of Utah

KK

About

Kerry K. Brown is an author at Brigham and Women's Hospital specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	2.2K
2	Public Health	2	2	967
3	Arts	1	1	82
4	Health Sciences	1	1	51
5	Natural Sciences	1	1	150

Kerry K. Brown

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10

Publications

3.2K

Citations

10

H-Index

	Year	Citations
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants Hutton M. Kearney, Erik C. Thorland, Kerry K. Brown, Genetics in Medicine Genetic TestingGenetic DisorderMedicineGeneticsAmerican College	2011	949
De novo mutations in histone-modifying genes in congenital heart disease Samir Zaidi, Murim Choi, Hiroko Wakimoto, Nature	2013	949
ACMG clinical laboratory standards for next-generation sequencing Heidi L. Rehm, Sherri J. Bale, Pınar Bayrak‐Toydemir, Genetics in Medicine Translational MedicineDna SequencingSequencingMedicineNext-generation Sequencing	2013	910
Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project Anne W. Higgins, Fowzan S. Alkuraya, Amy F. Bosco, The American Journal of Human Genetics BiologyChromatinChromosome DynamicsDevelopmental BiologyCell Division	2008	150
Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35) Kerry K. Brown, Jacob A. Reiss, Kate Crow, Human Genetics AudiologyNeurotologyCraniofacial DefectsCochlear ImplantArts	2009	82
<scp><i>HOXA</i></scp><i>2</i>Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss Kerry K. Brown, Lucas Moura Viana, Cecilia C. Helwig, Human Mutation Bilateral MicrotiaGeneticsNeurotologyMolecular GeneticsEpigenetics	2013	51
<i>NR2F1</i> deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness Kerry K. Brown, Fowzan S. Alkuraya, Michael Matos, American Journal of Medical Genetics Part A Paracentric InversionCytogeneticsGeneticsEpigeneticsTranslational Biology	2009	46
Molecular Diagnosis of Hearing Loss Kerry K. Brown, Heidi L. Rehm Current Protocols in Human Genetics	2012	28
X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of <i>POU3F4</i> G Anger, Susan Crocker, Kyle McKenzie, American Journal of Audiology	2014	22
Loss of <i>LDAH</i> associated with prostate cancer and hearing loss Benjamin Currall, Ming Chen, Richard Sallari, Human Molecular Genetics GeneticsGene DiscoveryDisease Gene IdentificationEpigeneticsGenetic Analysis	2018	18

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