Anastasia Fedick - Concepedia

Author

Anastasia Fedick

Reproductive Medicine Associates of New Jersey

Also Known As

A. Fedick, A.M. Fedick, Anastasia Fedick, Anastasia M Fedick, Anastasia M. Fedick, Knowles, Michael R.

Publications

668

Citations

H-Index

Concepts

All Affiliations

Reproductive Medicine Associates of New Jersey Johnson University Kingsbrook Jewish Medical Center Icahn School of Medicine at Mount Sinai Rutgers, The State University of New Jersey

About

Anastasia Fedick is an author at Reproductive Medicine Associates of New Jersey specializing in genetics, medicine, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	332
2	Public Health	3	3	232
3	Health Sciences	1	1	15
4	Epidemiology	1	1	12
5	Genetic Medicine	1	1	12

Anastasia Fedick

Publications

622

Citations

H-Index

Page 1

	Year	Citations
Evaluation of targeted next-generation sequencing–based preimplantation genetic diagnosis of monogenic disease Nathan R. Treff, Anastasia Fedick, Xin Tao, Fertility and Sterility SequencingPrenatal Genetic TestingMedicineGeneticsNext-generation Sequencing	2013	169
A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects Jinglan Zhang, Véronik Lachance, Adam Schaffner, PLoS Genetics Vps11 CausesGenetic LeukoencephalopathiesGeneticsPathologyDisease Gene Identification	2016	68
Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis Simon Edvardson, Angel Ashikov, Chaim Jalas, Journal of Medical Genetics	2013	66
Deficiency of the alkaline ceramidase ACER3 manifests in early childhood by progressive leukodystrophy Simon Edvardson, Jae Kyo Yi, Chaim Jalas, Journal of Medical Genetics	2016	53
Development and validation of concurrent preimplantation genetic diagnosis for single gene disorders and comprehensive chromosomal aneuploidy screening without whole genome amplification Rebekah Zimmerman, Chaim Jalas, Xin Tao, Fertility and Sterility Genetic TestingPrenatal Genetic TestingGenetic DisorderGeneticsPrenatal Genetic Screening	2015	51
Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population Anastasia Fedick, Chaim Jalas, Nathan R. Treff, Molecular Genetics & Genomic Medicine	2014	37
Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidy Alexandra Nguyen, Diego Marín, Anbo Zhou, Molecular Human Reproduction	2017	36
Leukoencephalopathy and early death associated with an Ashkenazi-Jewish founder mutation in the Hikeshi gene Simon Edvardson, Shingo Kose, Chaim Jalas, Journal of Medical Genetics	2015	34
High-Throughput Carrier Screening Using TaqMan Allelic Discrimination Anastasia Fedick, Jing Su, Chaim Jalas, PLoS ONE	2013	29
Carrier screening of <i>RTEL1</i> mutations in the Ashkenazi Jewish population Anastasia Fedick, Lijun Shi, Chaim Jalas, Clinical Genetics	2014	21

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