S. L. Sherman

1.4k total citations
18 papers, 1.0k citations indexed

About

S. L. Sherman is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, S. L. Sherman has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in S. L. Sherman's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (4 papers). S. L. Sherman is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (4 papers). S. L. Sherman collaborates with scholars based in United States, United Kingdom and Australia. S. L. Sherman's co-authors include Terry Hassold, Sallie B. Freeman, Dorothy Pettay, Neil E. Lamb, Michelle Merrill, P. A. Jacobs, David C. Page, Allison E. Ashley‐Koch, Paula W. Yoon and W. Dana Flanders and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Epidemiologic Reviews.

In The Last Decade

S. L. Sherman

18 papers receiving 996 citations

Peers

Countries citing papers authored by S. L. Sherman

Since Specialization

Citations

This map shows the geographic impact of S. 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 S. 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 S. L. Sherman more than expected).

Fields of papers citing papers by S. L. Sherman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of S. L. Sherman. A scholar is included among the top collaborators of S. 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 S. L. Sherman. S. 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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18 of 18 papers shown

#	Work	Indexed citations
1	Co‐occurring diagnoses among FMR1 premutation allele carriers 2010 ·Clinical Genetics ·(unknown), (unknown), S. L. Sherman	71
2	Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome Projects 2009 ·Clinical Genetics ·(unknown), (unknown), (unknown), (unknown), Charlotte M. Druschel, (unknown), S. L. Sherman	70
3	Effect of meiotic recombination on the production of aneuploid gametes in humans 2005 ·Cytogenetic and Genome Research ·Neil E. Lamb, S. L. Sherman, Terry Hassold	121
4	Analytic strategies for stroke genetics 2002 ·(unknown), Barney J. Stern, S. L. Sherman	1
5	FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? 2000 ·The American Journal of Human Genetics ·(unknown), Frédéric Rousseau, (unknown), (unknown), (unknown), (unknown), Helle Hjalgrim, Elke Holinski‐Feder, R. Frank Kooy, John Longshore, Janet L. Macpherson, J.-L. Mandel, Gert Matthijs, S. L. Sherman, Peter Steinbach, (unknown), Harriet von Koskull, (unknown)	2
6	Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1 1998 ·Human Molecular Genetics ·Chris Gunter, William Paradee, Dana C. Crawford, (unknown), Jane Newman, Catherine B. Kunst, David L. Nelson, Charles E. Schwartz, Anna Murray, John MacPherson, S. L. Sherman, Stephen T. Warren	59
7	A branching non‐linear autoregressive model for the transmission of the fragile X dynamic repeat mutation 1998 ·Annals of Human Genetics ·Richard Huggins, Danuta Z. Loesch, S. L. Sherman	2
8	Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome 1998 ·Chromosoma ·Joseph Shen, S. L. Sherman, Terry Hassold	14
9	Evolving Methods in Genetic Epidemiology. IV. Approaches to Non-Mendelian Inheritance 1997 ·Epidemiologic Reviews ·S. L. Sherman	7
10	Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. 1996 ·PubMed ·Paula W. Yoon, Sallie B. Freeman, S. L. Sherman, Lisa F. Taft, Yan Gu, Dorothy Pettay, W. Dana Flanders, Muin J. Khoury, Terry Hassold	145
11	Familial transmission of the FMR1 CGG repeat. 1996 ·PubMed ·Sarah L. Nolin, F A Lewis, (unknown), George E. Houck, Anne Glicksman, Pornprot Limprasert, (unknown), Ning Zhong, Allison E. Ashley‐Koch, (unknown), S. L. Sherman, W. Ted Brown	146
12	Statistical models for trisomic phenotypes. 1996 ·PubMed ·Neil E. Lamb, Eleanor Feingold, S. L. Sherman	4
13	Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. 1995 ·PubMed ·Terry Hassold, Michelle Merrill, (unknown), Sallie B. Freeman, S. L. Sherman	177
14	Population dynamics of a meiotic/mitotic expansion model for the fragile X syndrome. 1995 ·PubMed ·Allison E. Ashley‐Koch, S. L. Sherman	29
15	XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. 1991 ·PubMed ·Terry Hassold, S. L. Sherman, Dorothy Pettay, David C. Page, P. A. Jacobs	148
16	Investigation of the twinning rate in families with the fragile X syndrome 1988 ·American Journal of Medical Genetics ·S. L. Sherman, Gillian Turner, Leslie J. Sheffield, Susan T. Laing, Hazel M. Robinson	6
17	A strategy for multipoint ordering: Example of the 11p markers 1986 ·Genetic Epidemiology ·D. Timothy Bishop, S. L. Sherman	1
18	A revised map of chromosome 1 1984 ·Annals of Human Genetics ·S. L. Sherman, Jaime S. King, E.B. Robson, S Yee	21

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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