Susan H. Black

2.3k total citations
41 papers, 1.2k citations indexed

About

Susan H. Black is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Susan H. Black has authored 41 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Pediatrics, Perinatology and Child Health, 15 papers in Genetics and 9 papers in Molecular Biology. Recurrent topics in Susan H. Black's work include Prenatal Screening and Diagnostics (15 papers), Assisted Reproductive Technology and Twin Pregnancy (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Susan H. Black is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Assisted Reproductive Technology and Twin Pregnancy (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Susan H. Black collaborates with scholars based in United States, United Kingdom and France. Susan H. Black's co-authors include Joseph D. Schulman, Edward F. Fugger, Keyvan Keyvanfar, Andrew Dorfmann, JosephD. Schulman, David H. Ledbetter, Gene Levinson, G. Harton, P. N. Howard‐Peebles and Susan B. Olson and has published in prestigious journals such as New England Journal of Medicine, Neurology and The Journal of Pediatrics.

In The Last Decade

Susan H. Black

40 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Susan H. Black United States 20 632 505 275 166 159 41 1.2k
E.J.T. Winsor Canada 20 596 0.9× 450 0.9× 283 1.0× 242 1.5× 16 0.1× 46 1.2k
Joseph Shen United States 16 481 0.8× 598 1.2× 678 2.5× 85 0.5× 81 0.5× 26 1.3k
Kenneth L. Garver United States 11 225 0.4× 260 0.5× 160 0.6× 187 1.1× 43 0.3× 24 712
R. Penketh United Kingdom 19 485 0.8× 238 0.5× 375 1.4× 145 0.9× 145 0.9× 49 1.1k
Ilse Feenstra Netherlands 19 377 0.6× 731 1.4× 479 1.7× 69 0.4× 20 0.1× 45 1.3k
Jos Dreesen Netherlands 17 382 0.6× 314 0.6× 372 1.4× 107 0.6× 78 0.5× 32 898
Helene Stroh United States 14 251 0.4× 170 0.3× 244 0.9× 84 0.5× 31 0.2× 20 671
I. Liebaers Belgium 34 1.7k 2.6× 964 1.9× 818 3.0× 246 1.5× 1.1k 7.0× 80 3.0k
M O Rethoré France 21 395 0.6× 754 1.5× 599 2.2× 115 0.7× 24 0.2× 62 1.5k
M. Ray Canada 15 377 0.6× 731 1.4× 391 1.4× 73 0.4× 61 0.4× 36 1.1k

Countries citing papers authored by Susan H. Black

Since Specialization
Citations

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

Fields of papers citing papers by Susan H. Black

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan H. Black

This figure shows the co-authorship network connecting the top 25 collaborators of Susan H. Black. A scholar is included among the top collaborators of Susan H. Black 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 H. Black. Susan H. Black 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
3.
Stern, H., et al.. (2002). Non‐disclosing preimplantation genetic diagnosis for Huntington disease. Prenatal Diagnosis. 22(6). 503–507. 34 indexed citations
4.
Opsahl, Michael S., et al.. (2001). Clinical Assisted Reproduction: The Number of Embryos Available for Transfer Predicts Successful Pregnancy Outcome in Women over 39 Years with Normal Ovarian Hormonal Reserve Testing. Journal of Assisted Reproduction and Genetics. 18(10). 551–556. 18 indexed citations
5.
Toudjarska, Iva, M W Kilpatrick, Peter Lembessis, et al.. (2001). Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis. American Journal of Medical Genetics. 99(4). 294–302. 11 indexed citations
8.
Christian, Susan L., Ann C. M. Smith, Michelle Macha, et al.. (1996). PRENATAL DIAGNOSIS OF UNIPARENTAL DISOMY 15 FOLLOWING TRISOMY 15 MOSAICISM. Prenatal Diagnosis. 16(4). 323–332. 55 indexed citations
9.
Kilpatrick, M W, G. Harton, Leonidas A. Phylactou, et al.. (1996). Preimplantation Genetic Diagnosis in Marfan Syndrome. Fetal Diagnosis and Therapy. 11(6). 402–406. 8 indexed citations
10.
Black, Susan H., Lee Fallon, Anne Maddalena, et al.. (1996). Molecular fragile X screening in normal populations. American Journal of Medical Genetics. 64(1). 181–183. 4 indexed citations
11.
Harton, G., Petros Tsipouras, Edward F. Fugger, et al.. (1996). Preimplantation genetic testing for Marfan syndrome. Molecular Human Reproduction. 2(9). 713–715. 33 indexed citations
12.
Huffman, J.L., Jianfeng Wu, Frances T. Palmer, et al.. (1995). Diagnosing and preventing inherited disease: Nucleated erythrocytes in maternal blood: quantity and quality of fetal cells in enriched populations. Human Reproduction. 10(9). 2510–2515. 42 indexed citations
13.
Black, Susan H.. (1994). Preimplantation genetic diagnosis. Current Opinion in Pediatrics. 6(6). 712–716. 9 indexed citations
14.
Levinson, Gene, Anne Maddalena, Frances T. Palmer, et al.. (1994). Improved sizing of fragile X CCG repeats by nested polymerase chain reaction. American Journal of Medical Genetics. 51(4). 527–534. 35 indexed citations
15.
Huang, Bing, Bonnie Anne Salbert, J.A. Brown, et al.. (1994). Mental retardation and Ullrich‐Turner syndrome in cases with 45,X/46,X,+ mar: Additional support for the loss of the X‐inactivation center hypothesis. American Journal of Medical Genetics. 52(2). 136–145. 19 indexed citations
16.
Pergament, Eugene, JosephD. Schulman, Karen L. Copeland, et al.. (1992). The risk and efficacy of chorionic villus sampling in multiple gestations. Prenatal Diagnosis. 12(5). 377–384. 53 indexed citations
17.
Kalousek, Dagmar K., P. N. Howard‐Peebles, Susan B. Olson, et al.. (1991). Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism. Prenatal Diagnosis. 11(10). 743–750. 153 indexed citations
18.
Costakos, Deborah M., et al.. (1990). Chorionic villus sampling mosaicism: counseling issues.. PubMed. 26(3). 64–8. 1 indexed citations
19.
Sidransky, Ellen, et al.. (1990). Transvaginal chorionic villus sampling. Prenatal Diagnosis. 10(9). 583–586. 6 indexed citations
20.
Rizzo, William B., Debra A. Craft, Susan H. Black, et al.. (1989). Sjögren-Larsson syndrome: Inherited defect in the fatty alcohol cycle. The Journal of Pediatrics. 115(2). 228–234. 53 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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