Sharon L. Wenger

3.0k citations
83 papers · 1.6k indexed · h-index 24
Topics
Genomic variations and chromosomal abnormalities (30 papers)Genetics and Neurodevelopmental Disorders (15 papers)Prenatal Screening and Diagnostics (12 papers)
Journals
Proceedings of the National Academy of SciencesThe LancetSHILAP Revista de lepidopterología

In The Last Decade

Sharon L. Wenger

83 papers receiving 1.5k citations

Peers

Sharon L. Wenger
Comparison fields: 5 of 108
  • Genetics 985
  • Molecular Biology 790
  • Plant Science 243
  • Pediatrics, Perinatology and Child Health 231
  • Cognitive Neuroscience 155
Replace Andreas Rump with:
Andreas Rump Germany
Zohra Rahmani France
Toni R. Prezant United States
Young‐Wook Cho United States
Claudia Gonzaga‐Jauregui United States
Valentina Massa Italy
Birgit Carlsson Sweden
Nader Ghebranious United States
F. Arwert Netherlands
Nobuaki Wakamatsu Japan
Sharon L. Wenger relative to Andreas Rump Germany Andreas Rump's profile →
Citations per field
00.5×7.4×
Andreas Rump · 1×
Citations per year

Countries citing papers authored by Sharon L. Wenger

Since Specialization
Citations

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

Fields of papers citing papers by Sharon L. Wenger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sharon L. Wenger

This figure shows the co-authorship network connecting the top 25 collaborators of Sharon L. Wenger. A scholar is included among the top collaborators of Sharon L. Wenger 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 Sharon L. Wenger. Sharon L. Wenger 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
#WorkIndexed citations
1 5
2 22
3
Unusual Pattern of Bone Marrow Somatic Mutation in Pediatric Patients Referred for Cytogenetic Analysis
1
4 7
5 85
6 7
7 43
8 29
9 17
10 7
11 1
12 25
13 7
14 25
15 15
16 11
17 15
18 41
19 23
20 5

About Sharon L. Wenger

Sharon L. Wenger is a scholar working on Genetics, Developmental Biology and Hematology, having authored 83 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Genetics and Neurodevelopmental Disorders (15 papers) and Prenatal Screening and Diagnostics (12 papers). The work is most often cited by research in Genetics (985 citations), Pediatrics, Perinatology and Child Health (231 citations) and Developmental Biology (25 citations). Sharon L. Wenger has collaborated with scholars based in United States, Austria and India. Frequent co-authors include Mark W. Steele, Stephen G. Grant, Marybeth Hummel, James H. Cummins, Jennifer A. Scott, Aravinda Chakravarti, Linda M. Sargent, Wendy L. Golden, Narendra K. Bairwa and R. Bamezai. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Lancet and SHILAP Revista de lepidopterología.

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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