Brian E. Ward

3.5k total citations · 1 hit paper
41 papers, 2.6k citations indexed

About

Brian E. Ward is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Brian E. Ward has authored 41 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 15 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Brian E. Ward's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (12 papers) and BRCA gene mutations in cancer (9 papers). Brian E. Ward is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (12 papers) and BRCA gene mutations in cancer (9 papers). Brian E. Ward collaborates with scholars based in United States, Germany and Denmark. Brian E. Ward's co-authors include Thomas Scholl, Amie M. Deffenbaugh, Julia Reid, Wayne W. Grody, Elaine Lyon, Soma Das, C. Sue Richards, Daniel B. Bellissimo, Madhuri Hegde and Sherri J. Bale and has published in prestigious journals such as JAMA, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Brian E. Ward

40 papers receiving 2.5k 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.

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

2008 569 citations C. Sue Richards, Sherri J. Bale et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brian E. Ward United States	25	1.6k	870	485	446	406	41	2.6k
Marjan M. Weiss Netherlands	29	992 0.6×	1.0k 1.2×	737 1.5×	362 0.8×	715 1.8×	87	2.9k
Peter Papenhausen United States	20	706 0.4×	872 1.0×	158 0.3×	319 0.7×	205 0.5×	63	1.8k
Aliza Amiel Israel	27	613 0.4×	814 0.9×	236 0.5×	874 2.0×	130 0.3×	159	2.6k
B A Ponder United Kingdom	25	1.3k 0.8×	1.1k 1.2×	483 1.0×	79 0.2×	444 1.1×	39	2.7k
Michelle M. LeBeau United States	24	568 0.4×	2.1k 2.4×	413 0.9×	187 0.4×	357 0.9×	43	5.4k
Akira Yajima Japan	30	475 0.3×	689 0.8×	168 0.3×	433 1.0×	181 0.4×	174	3.0k
Eileen Bryant United States	42	523 0.3×	1.3k 1.5×	209 0.4×	309 0.7×	179 0.4×	82	5.3k
Stephen Francis United States	23	797 0.5×	834 1.0×	1.0k 2.1×	210 0.5×	373 0.9×	73	3.3k
Janette Lamb United States	24	487 0.3×	838 1.0×	147 0.3×	211 0.5×	159 0.4×	45	2.6k
Vaidehi Jobanputra United States	23	521 0.3×	456 0.5×	207 0.4×	221 0.5×	211 0.5×	79	1.3k

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-authorship network of co-authors of Brian E. Ward

This figure shows the co-authorship network connecting the top 25 collaborators of Brian E. Ward. A scholar is included among the top collaborators of Brian E. Ward 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 Brian E. Ward. Brian E. Ward 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

Hall, Michael J., Julia Reid, Lynn Anne Burbidge, et al.. (2009). BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer. Cancer. 115(10). 2222–2233. 275 indexed citations

Richards, C. Sue, Sherri J. Bale, Daniel B. Bellissimo, et al.. (2008). ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007. Genetics in Medicine. 10(4). 294–300. 569 indexed citations breakdown →

Balmañà, Judith, David H. Stockwell, Ewout W. Steyerberg, et al.. (2006). Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome. JAMA. 296(12). 1469–1469. 135 indexed citations

Ward, Benjamin D., Brant C. Hendrickson, Thaddeus Judkins, et al.. (2005). A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with Widely Dispersed Primer Sets. Journal of Molecular Diagnostics. 7(1). 139–142. 8 indexed citations

Hendrickson, Brant C., Thaddeus Judkins, Benjamin D. Ward, et al.. (2005). Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families. Genes Chromosomes and Cancer. 43(3). 309–313. 43 indexed citations

Nielsen, David R., Brant C. Hendrickson, Michael T. Pyne, et al.. (2003). A Biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A→C is a mutation. Journal of Human Genetics. 48(8). 399–403. 13 indexed citations

Frank, Thomas, Amie M. Deffenbaugh, Julia Reid, et al.. (2002). Clinical Characteristics of Individuals With Germline Mutations in BRCA1 and BRCA2: Analysis of 10,000 Individuals. Journal of Clinical Oncology. 20(6). 1480–1490. 455 indexed citations

Pyne, Michael T., et al.. (1999). A characterization of genetic variants in BRCA1 intron 8 identifies a mutation and a polymorphism. PubMed. 406(2-4). 101–107. 5 indexed citations

Sampson, Jone E., et al.. (1997). Fetal origin of amniotic fluid polymorphonuclear leukocytes. American Journal of Obstetrics and Gynecology. 176(1). 77–81. 124 indexed citations

10.

D’Alton, Mary E., Fergal D. Malone, David Chelmow, Brian E. Ward, & Diana W. Bianchi. (1997). Defining the role of fluorescence in situ hybridization on uncultured amniocytes for prenatal diagnosis of aneuploidies. American Journal of Obstetrics and Gynecology. 176(4). 769–776. 31 indexed citations

11.

Winsor, E.J.T., et al.. (1996). MATERNAL CELL CONTAMINATION IN UNCULTURED AMNIOTIC FLUID. Prenatal Diagnosis. 16(1). 49–54. 45 indexed citations

12.

Gersen, Steven L., et al.. (1995). Rapid prenatal diagnosis of 14 cases of triploidy using fish with multiple probes. Prenatal Diagnosis. 15(1). 1–5. 12 indexed citations

13.

Skupski, Daniel, et al.. (1994). Rapid Exclusion of Chromosomal Aneuploidies by Fluorescence in situ Hybridization prior to Fetal Surgery for Obstructive Uropathy – A Case Report. Fetal Diagnosis and Therapy. 9(5). 353–356. 4 indexed citations

14.

Isada, Nelson B., Roderick F. Hume, Mark P. Johnson, et al.. (1994). Fluorescent in situ Hybridization and Second-Trimester Sonographic Anomalies: Uses and Limitations. Fetal Diagnosis and Therapy. 9(6). 367–370. 7 indexed citations

15.

Ward, Brian E., et al.. (1992). Papillary immature metaplasia of the cervix: a distinct subset of exophytic cervical condyloma associated with HPV-6/11 nucleic acids.. PubMed. 5(4). 391–5. 24 indexed citations

16.

Ward, Brian E., et al.. (1990). Cytologic Correlates of Cervical Papillomavirus Infection. International Journal of Gynecological Pathology. 9(4). 297–305. 15 indexed citations

17.

Ward, Brian E., Robert E. Fechner, & Stacey E. Mills. (1990). Carcinoma Arising in Oncocytic Schneiderian Papilloma. The American Journal of Surgical Pathology. 14(4). 364–369. 25 indexed citations

18.

Crum, Christopher P., et al.. (1989). Topography of early HPV 16 transcription in high-grade genital precancers.. PubMed. 134(6). 1183–8. 27 indexed citations

19.

Franquemont, Douglas W., Brian E. Ward, Willie A. Andersen, & Christopher P. Crum. (1989). Prediction of ‘High-Risk’ Cervical Papillomavirus Infection by Biopsy Morphology. American Journal of Clinical Pathology. 92(5). 577–582. 29 indexed citations

20.

Ward, Brian E., et al.. (1988). Isochromosome 12p mosaicism (Pallister‐Killian syndrome): Newborn diagnosis by direct bone marrow analysis. American Journal of Medical Genetics. 31(4). 835–839. 47 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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