Stephanie L. Sherman

22.6k total citations · 1 hit paper
208 papers, 11.6k citations indexed

About

Stephanie L. Sherman is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Stephanie L. Sherman has authored 208 papers receiving a total of 11.6k indexed citations (citations by other indexed papers that have themselves been cited), including 149 papers in Genetics, 71 papers in Cognitive Neuroscience and 68 papers in Molecular Biology. Recurrent topics in Stephanie L. Sherman's work include Genetics and Neurodevelopmental Disorders (100 papers), Autism Spectrum Disorder Research (71 papers) and Genomic variations and chromosomal abnormalities (51 papers). Stephanie L. Sherman is often cited by papers focused on Genetics and Neurodevelopmental Disorders (100 papers), Autism Spectrum Disorder Research (71 papers) and Genomic variations and chromosomal abnormalities (51 papers). Stephanie L. Sherman collaborates with scholars based in United States, United Kingdom and Netherlands. Stephanie L. Sherman's co-authors include Emily G. Allen, Terry Hassold, Sallie B. Freeman, Dana C. Crawford, Juan Acuña, Eleanor Feingold, Lisa F. Taft, Ann Abramowitz, Lora Bean and Gillian Turner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and JAMA.

In The Last Decade

Stephanie L. Sherman

206 papers receiving 11.2k citations

Hit Papers

align trajectories

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.

Down syndrome

2020 491 citations Stephanie L. Sherman, Roger H. Reeves et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephanie L. Sherman United States	55	6.8k	4.2k	3.6k	2.2k	2.1k	208	11.6k
Merlin G. Butler United States	60	10.4k 1.5×	5.8k 1.4×	1.9k 0.5×	3.0k 1.4×	509 0.2×	382	14.5k
Allison E. Ashley‐Koch United States	48	1.8k 0.3×	2.2k 0.5×	1.6k 0.4×	802 0.4×	517 0.2×	210	8.3k
Ignatia B. Van den Veyver United States	30	4.7k 0.7×	3.4k 0.8×	1.9k 0.5×	1.6k 0.7×	421 0.2×	105	6.7k
Bengt Hagberg Sweden	55	4.9k 0.7×	3.0k 0.7×	3.5k 1.0×	4.2k 1.9×	326 0.2×	236	12.1k
Dale R. Nyholt Australia	47	4.6k 0.7×	2.5k 0.6×	938 0.3×	498 0.2×	446 0.2×	178	10.9k
Joachim Hallmayer United States	56	3.7k 0.5×	3.9k 0.9×	4.0k 1.1×	604 0.3×	286 0.1×	174	11.7k
Rosanna Weksberg Canada	55	5.5k 0.8×	7.2k 1.7×	703 0.2×	3.1k 1.4×	482 0.2×	235	11.2k
Judith L. Ross United States	59	5.9k 0.9×	4.3k 1.0×	1.4k 0.4×	1.4k 0.6×	500 0.2×	212	10.0k
Eden R. Martin United States	57	4.1k 0.6×	4.4k 1.0×	1.5k 0.4×	250 0.1×	748 0.4×	241	11.2k
Stacey S. Cherny Hong Kong	45	5.3k 0.8×	3.3k 0.8×	677 0.2×	395 0.2×	347 0.2×	164	11.2k

Countries citing papers authored by Stephanie L. Sherman

Since Specialization

Citations

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

Fields of papers citing papers by Stephanie L. Sherman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephanie L. Sherman. 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 Stephanie L. Sherman. The network helps show where Stephanie L. Sherman may publish in the future.

Co-authorship network of co-authors of Stephanie L. Sherman

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie L. Sherman. A scholar is included among the top collaborators of Stephanie L. Sherman 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 Stephanie L. Sherman. Stephanie L. Sherman 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

Ali, Nadia, et al.. (2022). The diagnostic experience of women with fragile X–associated primary ovarian insufficiency (FXPOI). Journal of Assisted Reproduction and Genetics. 40(1). 179–190. 8 indexed citations

Albizua, Igor, Krista Charen, Lisa Shubeck, et al.. (2022). Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Molecular Genetics & Genomic Medicine. 10(8). e2001–e2001. 4 indexed citations

Charen, Krista, Lisa Shubeck, Allyn McConkie‐Rosell, et al.. (2021). Men with an FMR1 premutation and their health education needs. Journal of Genetic Counseling. 30(4). 1156–1167. 1 indexed citations

Abbeduto, Leonard, Elizabeth Berry‐Kravis, Audra Sterling, et al.. (2020). Expressive language sampling as a source of outcome measures for treatment studies in fragile X syndrome: feasibility, practice effects, test-retest reliability, and construct validity. Journal of Neurodevelopmental Disorders. 12(1). 10–10. 39 indexed citations

Nolin, Sarah L., Anne Glicksman, Emily G. Allen, et al.. (2019). Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles. American Journal of Medical Genetics Part A. 179(7). 1148–1156. 47 indexed citations

Rambo‐Martin, Benjamin L., David J. Cutler, Lora Jh Bean, et al.. (2017). Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 Genes Genomes Genetics. 8(1). 105–111. 11 indexed citations

Kaufmann, Walter E., Sharon A. Kidd, Howard Andrews, et al.. (2017). Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment. PEDIATRICS. 139(Supplement_3). S194–S206. 186 indexed citations

Mailick, Marsha R., Jinkuk Hong, Jan S. Greenberg, Leann E. Smith, & Stephanie L. Sherman. (2014). Curvilinear association of CGG repeats and age at menopause in women with FMR1 premutation expansions. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(8). 705–711. 49 indexed citations

Li, Huiqing, Donna Klinedinst, Valerie B. DeLeon, et al.. (2012). Genetic Modifiers Predisposing to Congenital Heart Disease in the Sensitized Down Syndrome Population. Circulation Cardiovascular Genetics. 5(3). 301–308. 42 indexed citations

10.

Abrams, Liane, Amy Cronister, W. Ted Brown, et al.. (2012). Newborn, Carrier, and Early Childhood Screening Recommendations for Fragile X. PEDIATRICS. 130(6). 1126–1135. 29 indexed citations

11.

Allen, Emily G., Jessica Ezzell Hunter, Jorge L. Juncos, et al.. (2011). Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.. Neuropsychology. 25(3). 404–411. 15 indexed citations

12.

Coffee, Bradford, et al.. (2009). Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA. The American Journal of Human Genetics. 85(4). 503–514. 304 indexed citations

13.

Allen, Emily G., Krista Charen, James R. Giles, et al.. (2008). Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study. Human Reproduction. 23(5). 1220–1225. 64 indexed citations

14.

Hunter, Jessica Ezzell, Michael P. Epstein, Stuart W. Tinker, Krista Charen, & Stephanie L. Sherman. (2008). Fragile X‐associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. Genetic Epidemiology. 32(6). 553–559. 28 indexed citations

15.

Hunter, Jessica Ezzell, Emily G. Allen, Ann Abramowitz, et al.. (2008). No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50. The American Journal of Human Genetics. 83(6). 692–702. 61 indexed citations

16.

McConkie‐Rosell, Allyn, Liane Abrams, Brenda Finucane, et al.. (2007). Recommendations from Multi‐disciplinary Focus Groups on Cascade Testing and Genetic Counseling for Fragile X‐associated Disorders. Journal of Genetic Counseling. 16(5). 593–606. 48 indexed citations

17.

Wittenberger, Michael D., Randi J. Hagerman, Stephanie L. Sherman, et al.. (2006). The FMR1 premutation and reproduction. Fertility and Sterility. 87(3). 456–465. 297 indexed citations

18.

Sullivan, Amy K., Michele Marcus, Michael P. Epstein, et al.. (2004). Association of FMR1 repeat size with ovarian dysfunction. Human Reproduction. 20(2). 402–412. 345 indexed citations

19.

Crawford, Dana C., Kellen L. Meadows, James L. Newman, et al.. (2002). Prevalence of the fragile X syndrome in African‐Americans. American Journal of Medical Genetics. 110(3). 226–233. 113 indexed citations

20.

Crawford, Dana C., Juan Acuña, & Stephanie L. Sherman. (2001). FMR1 and the fragile X syndrome: Human genome epidemiology review. Genetics in Medicine. 3(5). 359–371. 477 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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