Brian E. Ward

3.5k citations
42 papers · 2.6k · 1 hit paper · h-index 25

Impact in

  • Genetics top 1%
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Cancer Genomics and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 13
    • BRCA gene mutations in cancer 9
    • CRISPR and Genetic Engineering 7
    • Molecular Biology Techniques and Applications 4

Brian E. Ward

40 papers receiving 2.6k citations

Brian E. Ward's Hit Papers

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 2008 · 574 citations
5740+6+12Years since publication100200300400500

Peers

Brian E. Ward
Comparison fields: 5 of 108
  • Genetics 1.4k
  • Cancer Research 325
  • Pediatrics, Perinatology and Child Health 383
  • Pathology and Forensic Medicine 320
  • Oncology 270
Replace Thomas Wagner with:
Thomas Wagner Austria
Marjan M. Weiss Netherlands
Kathleen Claes Belgium
Philip M. Iannaccone United States
Andrew J. Wallace United Kingdom
Curtis Gumbs United States
Ginevra Guanti Italy
Naofumi Ishikawa Japan
Karen E. Heath Spain
Wendy N. Cooper United Kingdom
Brian E. Ward relative to Thomas Wagner Austria Thomas Wagner's profile →
Citations per field
00.5×3.3×
Thomas Wagner · 1×
Citations per year

Countries citing papers authored by Brian E. Ward

Since Specialization
Citations

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

Fields of papers citing papers by Brian E. Ward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian E. Ward. 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 Brian E. Ward. The network helps show where Brian E. Ward may publish in the future.

Co-authors

The 25 scholars most cited alongside Brian E. Ward, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Brian E. Ward Line = papers co-authored together Brian E. Ward links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#Work
1
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
Hit paper breakdown →
2008574
2 2002456
3 2009278
4
Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens.
1993164
5 2006136
6 1997124
7 197988
8 199977
9 199466
10 200552
11 198847
12 199645
13 200543
14 197940
15
Cytogenetic studies in 100 couples with recurrent spontaneous abortions.
198035
16
Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH.
199634
17 199731
18 199031
19 198929
20 198929

About Brian E. Ward

Brian E. Ward is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Epidemiology and Plant Science, having authored 42 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (13 papers), BRCA gene mutations in cancer (9 papers), CRISPR and Genetic Engineering (7 papers), Chromosomal and Genetic Variations (6 papers), Cervical Cancer and HPV Research (5 papers), Molecular Biology Techniques and Applications (4 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Genetics (1.4k citations), Cancer Research (325 citations), Pediatrics, Perinatology and Child Health (383 citations), Pathology and Forensic Medicine (320 citations) and Oncology (270 citations). Brian E. Ward has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Thomas Scholl, Amie M. Deffenbaugh, Julia Reid, Soma Das, Madhuri Hegde, Daniel B. Bellissimo, Wayne W. Grody, C. Sue Richards, Sherri J. Bale and Elaine Lyon. Their work appears in journals such as Journal of Clinical Oncology, Prenatal Diagnosis, American Journal of Clinical Pathology, Fetal Diagnosis and Therapy and American Journal of Obstetrics and Gynecology.

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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