Judy Chernos

1.6k total citations
38 papers, 859 citations indexed

About

Judy Chernos is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Judy Chernos has authored 38 papers receiving a total of 859 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 15 papers in Pediatrics, Perinatology and Child Health and 14 papers in Molecular Biology. Recurrent topics in Judy Chernos's work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (14 papers) and Chromosomal and Genetic Variations (9 papers). Judy Chernos is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (14 papers) and Chromosomal and Genetic Variations (9 papers). Judy Chernos collaborates with scholars based in Canada, United States and Spain. Judy Chernos's co-authors include Renée H. Martin, Alfred Rademaker, Calvin Greene, Evelyn Ko, François P. Bernier, Leona Barclay, Michael K. Chan, Rebecca Sparkes, C. Templado and Martin J. Somerville and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Judy Chernos

37 papers receiving 785 citations

Peers

Judy Chernos

GENET

PPCH

PHEOH

Azzedine Aboura France

Susanne Ledig Germany

G. Lefort France

Ulrike Mau Germany

G. L. Terzoli Italy

Anahita Mohseni Meybodi Iran

Manuel Viotti United States

Liina Nagirnaja United States

Didier Theophile France

Frederick W. Luthardt United States

Azzedine Aboura France

Judy Chernos

525 ×1.0

GENET

311 ×0.8

258 ×0.9

PPCH

61 ×0.3

100 ×0.6

PHEOH

Citations per year, relative to Judy Chernos Judy Chernos (= 1×) peers Azzedine Aboura

Countries citing papers authored by Judy Chernos

Since Specialization

Citations

This map shows the geographic impact of Judy Chernos'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 Judy Chernos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judy Chernos more than expected).

Fields of papers citing papers by Judy Chernos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judy Chernos. 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 Judy Chernos. The network helps show where Judy Chernos may publish in the future.

Co-authorship network of co-authors of Judy Chernos

This figure shows the co-authorship network connecting the top 25 collaborators of Judy Chernos. A scholar is included among the top collaborators of Judy Chernos 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 Judy Chernos. Judy Chernos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lazier, Joanna, Deborah Fruitman, Julie Lauzon, et al.. (2016). Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies. Journal of Obstetrics and Gynaecology Canada. 38(7). 619–626. 11 indexed citations

Lazier, Joanna, Judy Chernos, & R. Brian Lowry. (2014). A 2q24.3q31.1 microdeletion found in a patient with Filippi‐like syndrome phenotype: A case report. American Journal of Medical Genetics Part A. 164(9). 2385–2387. 14 indexed citations

Lowry, R. Brian, et al.. (2013). Interstitial Deletions at 6q14.1q15 Associated with Developmental Delay and a Marfanoid Phenotype. Molecular Syndromology. 4(6). 280–284. 4 indexed citations

Dawson, Angelika J., Jean McGowan‐Jordan, Judy Chernos, et al.. (2011). Canadian College of Medical Geneticists Guidelines for the Indications, Analysis, and Reporting of Cancer Specimens. Current Oncology. 18(5). 250–255. 6 indexed citations

Khan, Faisal, Judy Chernos, Noureddine Berka, et al.. (2010). Nasal Epithelial Cells of Donor Origin after Allogeneic Hematopoietic Cell Transplantation are Generated at a Faster Rate in the First 3 Months Compared with Later Posttransplantation. Biology of Blood and Marrow Transplantation. 16(12). 1658–1664. 7 indexed citations

Sparkes, Rebecca, Shashirekha Shetty, Judy Chernos, Heather C Mefford, & A. Micheil Innes. (2009). Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling. Prenatal Diagnosis. 29(3). 283–286. 20 indexed citations

Meng, Guoliang, Shiying Liu, Roman Krawetz, et al.. (2008). A Novel Method for Generating Xeno-Free Human Feeder Cells for Human Embryonic Stem Cell Culture. Stem Cells and Development. 17(3). 413–422. 38 indexed citations

Sparkes, Rebecca, François P. Bernier, Judy Chernos, & Jo‐Ann Johnson. (2008). Suitability of Rapid Aneuploidy Detection for Prenatal Diagnosis. Journal of Obstetrics and Gynaecology Canada. 30(9). 781–787. 5 indexed citations

Innes, A. Micheil, et al.. (2008). An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier. American Journal of Medical Genetics Part A. 146A(8). 1067–1071.

10.

Somerville, Martin J., Lionel Willatt, Helen V. Firth, et al.. (2005). Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome. The American Journal of Human Genetics. 76(5). 865–876. 170 indexed citations

11.

McGillivray, Barbara, Sara Hamilton, Evelyn Ko, et al.. (2005). Unusual segregation products in sperm from a pericentric inversion 17 heterozygote. Human Genetics. 117(4). 357–365. 26 indexed citations

12.

Sparkes, Rebecca, et al.. (2005). Duplication of the 22q11.2 region associated with congenital cardiac disease. Cardiology in the Young. 15(2). 229–231. 17 indexed citations

13.

Ko, Evelyn, et al.. (2004). Analysis of chromosome segregation in sperm from a chromosome 2 inversion heterozygote and assessment of an interchromosomal effect. American Journal of Medical Genetics Part A. 127A(2). 139–143. 32 indexed citations

14.

Martin, Renée H., Alfred Rademaker, Calvin Greene, et al.. (2003). A Comparison of the Frequency of Sperm Chromosome Abnormalities in Men with Mild, Moderate, and Severe Oligozoospermia1. Biology of Reproduction. 69(2). 535–539. 83 indexed citations

15.

Martin, Renée H., Calvin Greene, Alfred Rademaker, Evelyn Ko, & Judy Chernos. (2003). Analysis of Aneuploidy in Spermatozoa From Testicular Biopsies From Men With Nonobstructive Azoospermia. Journal of Andrology. 24(1). 100–103. 32 indexed citations

16.

Hristova, Rositsa, Evelyn Ko, Calvin Greene, et al.. (2002). Chromosome Abnormalities in Sperm From Infertile Men with Asthenoteratozoospermia1. Biology of Reproduction. 66(6). 1781–1783. 54 indexed citations

17.

Yoon, Grace H., et al.. (2001). Association between congenital foot anomalies and gestational age at amniocentesis. Prenatal Diagnosis. 21(13). 1137–1141. 6 indexed citations

18.

Xu, Jie, Judy Chernos, François P. Bernier, & R. Brian Lowry. (2000). Characterization of an Interstitial Deletion del(13)(q22q32) Using Microdissection and Sequential FISH and G-Banding. Genetic Testing. 4(3). 279–282. 3 indexed citations

19.

Chernos, Judy, et al.. (1992). Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier. Clinical Genetics. 41(5). 266–269. 11 indexed citations

20.

Martin, Renée H., Judy Chernos, & Alfred Rademaker. (1991). Effect of cryopreservation on the frequency of chromosomal abnormalities and sex ratio in human sperm. Molecular Reproduction and Development. 30(2). 159–163. 33 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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