Matthew C. Dulik - Concepedia

Author

Matthew C. Dulik

Also Known As

Amendola, Laura M., Bowling, Kevin M., Conlin, Laura K., Hisama, Fuki M., M. C. Dulik, Matthew C Dulik, Matthew C. Dulik, Matthew Dulik, Matthew C. Dulik, McMullen, Carmit

Publications

3.7K

Citations

H-Index

Concepts

All Affiliations

University of Pennsylvania Children's Hospital of Philadelphia Harvard University University of Washington University of North Carolina at Chapel Hill

About

Matthew C. Dulik is an author at University of Pennsylvania specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	2.6K
2	Public Health	7	7	1.7K
3	Natural Sciences	3	3	264
4	Arts	1	1	39
5	Language Studies	1	1	17

Matthew C. Dulik

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium Laura M. Amendola, Gail P. Jarvik, Michael C. Leo, The American Journal of Human Genetics SequencingMedicineGeneticsNext-generation SequencingGenetic Epidemiology	2016	564
Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between Gail P. Jarvik, Laura M. Amendola, Jonathan S. Berg, The American Journal of Human Genetics Genomic ResultsGenetic TestingResearch ParticipantsGeneticsStatistical Genetics	2014	368
Actionable exomic incidental findings in 6503 participants: challenges of variant classification Laura M. Amendola, Michael O. Dorschner, Peggy D. Robertson, Genome Research Genome-wide Association StudyEpidemiologySequencingExome SequencingGenetics	2015	356
Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans Paul Brotherton, Wolfgang Haak, Jennifer E.L. Templeton, Nature Communications GeneticsEvolutionary BiologyPaleoanthropologyHuman OriginArchaeology	2013	227
Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation Elizabeth M. McCormick, Marie T. Lott, Matthew C. Dulik, Human Mutation Acmg/amp StandardsDnaGeneticsGenetic EpidemiologyDna Analysis	2020	169
Mitochondrial DNA and Y Chromosome Variation Provides Evidence for a Recent Common Ancestry between Native Americans and Indigenous Altaians Matthew C. Dulik, Sergey Zhadanov, L. P. Osipova, The American Journal of Human Genetics Human VariationNatural SciencesGeneticsEvolutionary BiologyMedicine	2012	162
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik, The American Journal of Human Genetics EpidemiologySequencingMedicineNext-generation SequencingGenomics	2016	161
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study Ragan Hart, Barbara B. Biesecker, Carrie L. Blout Zawatsky, Genetics in Medicine Genetic TestingClinical Genomic SequencingNext-generation SequencingGenetic EpidemiologyGenomics	2018	154
Germline gain-of-function mutations in AFF4 cause a developmental syndrome functionally linking the super elongation complex and cohesin Kosuke Izumi, Ryuichiro Nakato, Zhe Zhang, Nature Genetics Developmental AnomalyDevelopmental BiologyGenetic DisorderDevelopmental GeneticsGenetics	2015	144
Aboriginal Australian mitochondrial genome variation – an increased understanding of population antiquity and diversity Nano Nagle, Mannis van Oven, Stephen Wilcox, Scientific Reports	2017	117

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