Susan Klugman

5.2k total citations · 4 hit papers
57 papers, 2.2k citations indexed

About

Susan Klugman is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Susan Klugman has authored 57 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Pediatrics, Perinatology and Child Health, 27 papers in Genetics and 10 papers in Molecular Biology. Recurrent topics in Susan Klugman's work include Prenatal Screening and Diagnostics (32 papers), BRCA gene mutations in cancer (13 papers) and Genomic variations and chromosomal abnormalities (13 papers). Susan Klugman is often cited by papers focused on Prenatal Screening and Diagnostics (32 papers), BRCA gene mutations in cancer (13 papers) and Genomic variations and chromosomal abnormalities (13 papers). Susan Klugman collaborates with scholars based in United States, Canada and United Kingdom. Susan Klugman's co-authors include Anthony R. Gregg, Robert G. Best, Komal Bajaj, Kristin G. Monaghan, Brian G. Skotko, Ilan E. Timor‐Tritsch, Christine H. Comstock, Lorraine Dugoff, Sabrina Craigo and Honor M. Wolfe and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Obstetrics and Gynecology and PLoS Genetics.

In The Last Decade

Susan Klugman

51 papers receiving 2.1k citations

Hit Papers

Impact of Maternal Age on Obstetric Outcome 2005 2026 2012 2019 2005 2016 2021 2022 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Impact of Maternal Age on Obstetric Outcome
    2005 629 citations Fergal D. Malone, John Vidaver et al. profile →
  2. Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics
    2016 472 citations Anthony R. Gregg, Brian G. Skotko et al. Genetics in Medicine profile →
  3. Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)
    2021 221 citations Anthony R. Gregg, Mahmoud Aarabi et al. Genetics in Medicine profile →
  4. Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
    2022 101 citations J.S. Dungan, Susan Klugman et al. Genetics in Medicine profile →

Peers

Susan Klugman
Philip Wyatt Canada
Sylvie Langlois Canada
Lauren Lynch United States
Lisa Hui Australia
Karin J. Blakemore United States
Jo-Ann Johnson Canada
Ron Maymon Israel
Nanette Okun Canada
Mireille N. Bekker Netherlands
Eugene Pergament United States
Philip Wyatt Canada
Susan Klugman
Citations per year, relative to Susan Klugman Susan Klugman (= 1×) peers Philip Wyatt

Countries citing papers authored by Susan Klugman

Since Specialization
Citations

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

Fields of papers citing papers by Susan Klugman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Klugman

This figure shows the co-authorship network connecting the top 25 collaborators of Susan Klugman. A scholar is included among the top collaborators of Susan Klugman 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 Susan Klugman. Susan Klugman 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.
Pal, Tuya, Katherine Schon, Judith Balmañà, et al.. (2024). Management of individuals with heterozygous germline pathogenic variants in ATM: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(1). 101243–101243. 6 indexed citations
2.
Hanson, Helen, Laura M. Amendola, Judith Balmañà, et al.. (2023). Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(10). 100870–100870. 29 indexed citations
3.
Doulaveris, Georgios, et al.. (2022). Impact of introducing cell‐free DNA screening into clinical care on first trimester ultrasound. Prenatal Diagnosis. 42(2). 254–259. 7 indexed citations
4.
Gregg, Anthony R., Mahmoud Aarabi, Susan Klugman, et al.. (2022). Screening for Autosomal Recessive and X-Linked Conditions During Pregnancy and Preconception: A Practice Resource of the American College of Medical Genetics and Genomics (ACMG). Obstetrical & Gynecological Survey. 77(4). 193–196. 2 indexed citations
5.
Doulaveris, Georgios, et al.. (2021). Patient attitudes toward prenatal diagnostic testing during antenatal care in an urban population. Prenatal Diagnosis. 41(7). 888–895. 1 indexed citations
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8.
Gregg, Anthony R., Mahmoud Aarabi, Susan Klugman, et al.. (2021). Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(10). 1793–1806. 221 indexed citations breakdown →
9.
Skotko, Brian G., Megan Allyse, Komal Bajaj, et al.. (2019). Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations. Genetics in Medicine. 21(10). 2285–2292. 22 indexed citations
10.
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Goldwaser, Tamar & Susan Klugman. (2018). Cell-free DNA for the detection of fetal aneuploidy. Fertility and Sterility. 109(2). 195–200. 19 indexed citations
12.
King, Jennifer R. & Susan Klugman. (2018). Ethnicity-Based Carrier Screening. Obstetrics and Gynecology Clinics of North America. 45(1). 83–101. 18 indexed citations
13.
Gregg, Anthony R., Brian G. Skotko, Judith Benkendorf, et al.. (2017). Noninvasive Prenatal Screening for Fetal Aneuploidy, 2016 Update: A Position Statement of the American College of Medical Genetics and Genomics. Obstetrical & Gynecological Survey. 72(1). 6–8. 11 indexed citations
14.
Greb, Anne, et al.. (2016). Patient Perspectives on Intimate Partner Violence Discussion during Genetic Counseling Sessions. Journal of Genetic Counseling. 26(2). 261–271. 3 indexed citations
15.
Shani, Hagit, Tamar Goldwaser, Jennifer L. Keating, & Susan Klugman. (2015). Chromosomal abnormalities not currently detected by cell-free fetal DNA: a retrospective analysis at a single center. American Journal of Obstetrics and Gynecology. 214(6). 729.e1–729.e11. 29 indexed citations
16.
Klugman, Susan, Nicole Schreiber‐Agus, Shivani Nazareth, & Eric A. Evans. (2013). Detection of Carriers in the Ashkenazi Jewish Population: An Objective Comparison of High-Throughput Genotyping Versus Gene-by-Gene Testing. Genetic Testing and Molecular Biomarkers. 17(10). 763–767. 2 indexed citations
17.
Gross, Susan J., Komal Bajaj, David Garry, et al.. (2011). Rapid and novel prenatal molecular assay for detecting aneuploidies and microdeletion syndromes. Prenatal Diagnosis. 31(3). 259–266. 39 indexed citations
18.
Eddleman, Keith, Fergal D. Malone, Lisa Sullivan, et al.. (2007). Pregnancy Loss Rates After Midtrimester Amniocentesis. Obstetrical & Gynecological Survey. 62(3). 163–164. 11 indexed citations
19.
Lambert‐Messerlian, Geralyn, Lorraine Dugoff, John Vidaver, et al.. (2006). First- and Second-Trimester Down Syndrome Screening Markers in Pregnancies Achieved Through Assisted Reproductive Technologies (ART): A FASTER Trial Study. Obstetrical & Gynecological Survey. 61(12). 767–768. 1 indexed citations
20.
Cordero, Dwight R., Yael Goldberg, Donald Basel, et al.. (2006). Prenatal Sonographic Diagnosis of Grebe Syndrome. Journal of Ultrasound in Medicine. 25(1). 115–118. 1 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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