Anastasia Fedick

671 total citations
20 papers, 426 citations indexed

About

Anastasia Fedick is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anastasia Fedick has authored 20 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anastasia Fedick's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Cystic Fibrosis Research Advances (3 papers). Anastasia Fedick is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Cystic Fibrosis Research Advances (3 papers). Anastasia Fedick collaborates with scholars based in United States, Israel and Germany. Anastasia Fedick's co-authors include Nathan R. Treff, Chaim Jalas, Richard T. Scott, Xin Tao, Batsal Devkota, Deanne Taylor, Simon Edvardson, Orly Elpeleg, Jing Su and Lesley E. Northrop and has published in prestigious journals such as PLoS ONE, Fertility and Sterility and Genomics.

In The Last Decade

Anastasia Fedick

20 papers receiving 417 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Anastasia Fedick 217 169 139 60 45 20 426
Roxana Kariminejad 231 1.1× 136 0.8× 258 1.9× 23 0.4× 31 0.7× 40 683
Masanaga Muto 362 1.7× 189 1.1× 131 0.9× 159 2.6× 33 0.7× 20 712
Filippo Zambelli 344 1.6× 92 0.5× 59 0.4× 187 3.1× 12 0.3× 24 561
Luciana Ribeiro Montenegro 512 2.4× 100 0.6× 483 3.5× 124 2.1× 15 0.3× 46 957
Mônica M. França 255 1.2× 50 0.3× 236 1.7× 192 3.2× 16 0.4× 28 541
Emilie Ait‐Yahya 171 0.8× 42 0.2× 151 1.1× 114 1.9× 14 0.3× 18 366
Gregor Schlüter 246 1.1× 37 0.2× 186 1.3× 82 1.4× 13 0.3× 25 486
Nick Giannoukakis 146 0.7× 42 0.2× 129 0.9× 15 0.3× 33 0.7× 14 362
Katie M. Lowther 241 1.1× 56 0.3× 45 0.3× 271 4.5× 23 0.5× 19 449
Mengwen Hu 371 1.7× 46 0.3× 102 0.7× 280 4.7× 138 3.1× 52 640

Countries citing papers authored by Anastasia Fedick

Since Specialization
Citations

This map shows the geographic impact of Anastasia Fedick's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Anastasia Fedick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anastasia Fedick more than expected).

Fields of papers citing papers by Anastasia Fedick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anastasia Fedick. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Anastasia Fedick. The network helps show where Anastasia Fedick may publish in the future.

Co-authorship network of co-authors of Anastasia Fedick

This figure shows the co-authorship network connecting the top 25 collaborators of Anastasia Fedick. A scholar is included among the top collaborators of Anastasia Fedick based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anastasia Fedick. Anastasia Fedick is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Fedick, Anastasia, Jinglan Zhang, Lisa Edelmann, & Ruth Kornreich. (2018). Prenatal Diagnosis of Cystic Fibrosis. Methods in molecular biology. 1885. 221–231. 2 indexed citations
2.
Nguyen, Alexandra, Diego Marín, Anbo Zhou, et al.. (2017). Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidy. Molecular Human Reproduction. 23(6). 406–416. 28 indexed citations
3.
Zhang, Jinglan, Anastasia Fedick, Geping Zhao, et al.. (2016). Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment. Journal of Molecular Diagnostics. 18(2). 260–266. 12 indexed citations
4.
Webb, Bryn D., et al.. (2016). Identification of a novel pathogenic <em>OTOF</em> variant causative of nonsyndromic hearing loss with high frequency in the Ashkenazi Jewish population. The Application of Clinical Genetics. Volume 9. 141–146. 11 indexed citations
5.
Edvardson, Simon, Jae Kyo Yi, Chaim Jalas, et al.. (2016). Deficiency of the alkaline ceramidase ACER3 manifests in early childhood by progressive leukodystrophy. Journal of Medical Genetics. 53(6). 389–396. 36 indexed citations
6.
Zimmerman, Rebekah, Chaim Jalas, Xin Tao, et al.. (2015). Development and validation of concurrent preimplantation genetic diagnosis for single gene disorders and comprehensive chromosomal aneuploidy screening without whole genome amplification. Fertility and Sterility. 105(2). 286–294. 40 indexed citations
7.
Edvardson, Simon, Shingo Kose, Chaim Jalas, et al.. (2015). Leukoencephalopathy and early death associated with an Ashkenazi-Jewish founder mutation in the Hikeshi gene. Journal of Medical Genetics. 53(2). 132–137. 22 indexed citations
8.
Tao, Xin, Chaim Jalas, Anastasia Fedick, et al.. (2014). Rapid and concurrent comprehensive chromosome screening (CCS) and single gene disorder (SGD) PGD. Fertility and Sterility. 102(3). e183–e183. 1 indexed citations
9.
Fedick, Anastasia, Katharine J. Thompson, Eric J. Forman, et al.. (2014). Lack of association of KATNAL1 gene sequence variants and azoospermia in humans. Journal of Assisted Reproduction and Genetics. 31(8). 1065–1071. 5 indexed citations
10.
Anderson, Sylvia L., Chaim Jalas, Anastasia Fedick, et al.. (2014). A founder mutation in the TCIRG1 gene causes osteopetrosis in the Ashkenazi Jewish population. Clinical Genetics. 88(1). 74–79. 7 indexed citations
11.
Fedick, Anastasia, Chaim Jalas, Nathan R. Treff, Michael R. Knowles, & Maimoona A. Zariwala. (2014). Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population. Molecular Genetics & Genomic Medicine. 3(2). 137–142. 12 indexed citations
12.
Fedick, Anastasia, Lijun Shi, Chaim Jalas, et al.. (2014). Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population. Clinical Genetics. 88(2). 177–181. 14 indexed citations
13.
Treff, Nathan R., Anastasia Fedick, Xin Tao, et al.. (2013). Evaluation of targeted next-generation sequencing–based preimplantation genetic diagnosis of monogenic disease. Fertility and Sterility. 99(5). 1377–1384.e6. 130 indexed citations
14.
Fedick, Anastasia, Jing Su, Chaim Jalas, et al.. (2013). High-Throughput Carrier Screening Using TaqMan Allelic Discrimination. PLoS ONE. 8(3). e59722–e59722. 20 indexed citations
15.
Fedick, Anastasia, et al.. (2013). Carrier frequency of two BBS2 mutations in the Ashkenazi population. Clinical Genetics. 85(6). 578–582. 9 indexed citations
16.
Fedick, Anastasia, Chaim Jalas, & Nathan R. Treff. (2013). A deleterious mutation in the PEX2 gene causes Zellweger syndrome in individuals of Ashkenazi Jewish descent. Clinical Genetics. 85(4). 343–346. 5 indexed citations
17.
Webb, Bryn D., Tracy Brandt, Chaim Jalas, et al.. (2013). A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population. Clinical Genetics. 86(2). 155–160. 12 indexed citations
18.
Edvardson, Simon, Angel Ashikov, Chaim Jalas, et al.. (2013). Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis. Journal of Medical Genetics. 50(11). 733–739. 46 indexed citations
19.
Fedick, Anastasia, Jing Su, & Nathan R. Treff. (2012). Development of TaqMan allelic discrimination based genotyping of large DNA deletions. Genomics. 99(3). 127–131. 7 indexed citations
20.
Fedick, Anastasia, Jing Su, Chaim Jalas, & Nathan R. Treff. (2012). High-throughput real-time PCR-based genotyping without DNA purification. BMC Research Notes. 5(1). 573–573. 7 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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