Sarah Alliman

876 total citations
9 papers, 540 citations indexed

About

Sarah Alliman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Sarah Alliman has authored 9 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 2 papers in Molecular Biology. Recurrent topics in Sarah Alliman's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic Syndromes and Imprinting (2 papers). Sarah Alliman is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic Syndromes and Imprinting (2 papers). Sarah Alliman collaborates with scholars based in United States, Australia and Canada. Sarah Alliman's co-authors include Lisa G. Shaffer, Bassem A. Bejjani, Allen N. Lamb, Blake C. Ballif, Justine Coppinger, Ryan N. Traylor, Jill A. Rosenfeld, Sangeetha Mahadevan, Beth S. Torchia and Richard Person and has published in prestigious journals such as European Journal of Human Genetics, Obstetrical & Gynecological Survey and Clinical Genetics.

In The Last Decade

Sarah Alliman

9 papers receiving 497 citations

Peers

Countries citing papers authored by Sarah Alliman

Since Specialization

Citations

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

Fields of papers citing papers by Sarah Alliman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Alliman

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

#	Work	Indexed citations
1	The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes 2011 ·Prenatal Diagnosis ·Lisa G. Shaffer, Justine Coppinger, (unknown), Sarah Alliman, (unknown), Ryan N. Traylor, (unknown), (unknown), Allen N. Lamb, Roger A. Schultz, J. Britt Ravnan, Catherine D. Kashork, Beth S. Torchia, (unknown), Kyle Sundin, (unknown), (unknown), Stephanie Dallaire, Blake C. Ballif	33
2	Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array‐based comparative genomic hybridization 2011 ·American Journal of Medical Genetics Part A ·(unknown), Josiane Souza, Fábio R. Faucz, Vanessa Santos Sotomaior, Barbara R. DuPont, Frank Bartel, (unknown), Charles E. Schwartz, Cindy Skinner, Sarah Alliman, Salmo Raskin	22
3	A tale of two deletions: A report of two novel 20p13 → pter deletions 2010 ·American Journal of Medical Genetics Part A ·(unknown), Matthew Pastore, Gail E. Herman, Sarah Alliman, Jill A. Rosenfeld, David D. Weaver	11
4	Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome 2010 ·European Journal of Human Genetics ·Angela L. Duker, Blake C. Ballif, Erawati V. Bawle, Richard Person, Sangeetha Mahadevan, Sarah Alliman, (unknown), Ryan N. Traylor, Bassem A. Bejjani, Lisa G. Shaffer, Jill A. Rosenfeld, Allen N. Lamb, Trilochan Sahoo	236
5	Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2 2010 ·Clinical Genetics ·Sarah Alliman, Justine Coppinger, Janet Marcadier, Heidi Thiese, Pamela Brock, (unknown), Christine A. Weaver, Alexander Asamoah, Kathleen A. Leppig, Sarah Dyack, (unknown), Roger A. Schultz, (unknown), (unknown), (unknown)	20
6	Whole‐genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray 2009 ·Prenatal Diagnosis ·Justine Coppinger, Sarah Alliman, Allen N. Lamb, Beth S. Torchia, Bassem A. Bejjani, Lisa G. Shaffer	97
7	A Comparative Analysis of Ethical and Professional Challenges Experienced by Australian and U.S. Genetic Counselors 2009 ·Journal of Genetic Counseling ·Sarah Alliman, Patricia McCarthy Veach, Dianne M. Bartels, (unknown), (unknown), Bonnie S. LeRoy	17
8	Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens 2008 ·Prenatal Diagnosis ·Lisa G. Shaffer, Justine Coppinger, Sarah Alliman, Beth A. Torchia, Aaron Theisen, Blake C. Ballif, Bassem A. Bejjani	102
9	Comparison of Microarray-Based Detection Rates for Cytogenetic Abnormalities in Prenatal and Neonatal Specimens 2008 ·Obstetrical & Gynecological Survey ·Lisa G. Shaffer, Justine Coppinger, Sarah Alliman, Beth A. Torchia, Aaron Theisen, Blake C. Ballif, Bassem A. Bejjani	2

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.

Explore authors with similar magnitude of impact