Gail E. Herman

12.2k total citations · 3 hit papers
102 papers, 5.7k citations indexed

About

Gail E. Herman is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Gail E. Herman has authored 102 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 51 papers in Genetics and 13 papers in Cell Biology. Recurrent topics in Gail E. Herman's work include Genetics and Neurodevelopmental Disorders (18 papers), Cholesterol and Lipid Metabolism (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Gail E. Herman is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Cholesterol and Lipid Metabolism (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Gail E. Herman collaborates with scholars based in United States, United Kingdom and Canada. Gail E. Herman's co-authors include Forbes D. Porter, Paul Modrich, Richard I. Kelley, Matthew Pastore, Thomas W. Prior, Michael S. Watson, Kim L. McBride, Kent D. McKelvey, C. Sue Richards and David T. Miller and has published in prestigious journals such as New England Journal of Medicine, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Gail E. Herman

102 papers receiving 5.6k 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.

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

2016 1.0k citations Sarah S. Kalia, Sherri J. Bale et al. Genetics in Medicine profile →
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

2021 302 citations David T. Miller, Kristy Lee et al. Genetics in Medicine profile →
EFFECTS OF HIGH LEVELS OF DNA ADENINE METHYLATION ON METHYL-DIRECTED MISMATCH REPAIR IN ESCHERICHIA COLI

1983 245 citations Gail E. Herman et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gail E. Herman United States	33	3.2k	2.6k	688	534	517	102	5.7k
Harald H.H. Göring United States	40	2.2k 0.7×	2.1k 0.8×	399 0.6×	272 0.5×	582 1.1×	147	5.9k
Elizabeth Baker Australia	44	3.4k 1.0×	2.9k 1.1×	234 0.3×	318 0.6×	473 0.9×	116	6.7k
Arif B. Ekici Germany	42	2.6k 0.8×	1.6k 0.6×	308 0.4×	569 1.1×	311 0.6×	195	5.1k
Grant R. Sutherland Australia	58	7.0k 2.2×	4.9k 1.9×	542 0.8×	726 1.4×	493 1.0×	164	13.2k
Richard R. Meehan United Kingdom	49	6.8k 2.1×	2.7k 1.0×	460 0.7×	610 1.1×	360 0.7×	111	8.4k
Bruce D. Weintraub United States	52	2.5k 0.8×	1.4k 0.5×	782 1.1×	238 0.4×	478 0.9×	166	8.6k
Giulio Genovese United States	33	2.6k 0.8×	1.8k 0.7×	208 0.3×	434 0.8×	334 0.6×	67	6.8k
Carmen Ayuso Spain	50	5.7k 1.8×	2.2k 0.8×	507 0.7×	337 0.6×	210 0.4×	351	9.0k
Kirby D. Smith United States	39	4.6k 1.4×	1.5k 0.6×	389 0.6×	355 0.7×	900 1.7×	93	6.3k
Jean-Marc Lalouel United States	41	2.1k 0.6×	2.2k 0.8×	1.1k 1.6×	394 0.7×	404 0.8×	111	7.2k

Countries citing papers authored by Gail E. Herman

Since Specialization

Citations

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

Fields of papers citing papers by Gail E. Herman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gail E. Herman

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

Miller, David T., Kristy Lee, Allan Gordon, et al.. (2021). Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(8). 1391–1398. 142 indexed citations

Kalia, Sarah S., Sherri J. Bale, Wendy K. Chung, et al.. (2016). Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. Genetics in Medicine. 19(2). 249–255. 1023 indexed citations breakdown →

Gabitova, Linara, Diana Restifo, Andrey Gorin, et al.. (2015). Endogenous Sterol Metabolites Regulate Growth of EGFR/KRAS-Dependent Tumors via LXR. Cell Reports. 12(11). 1927–1938. 61 indexed citations

Scheuner, Maren T., Judith Benkendorf, Bruce Bowdish, et al.. (2014). Reporting genomic secondary findings: ACMG members weigh in. Genetics in Medicine. 17(1). 27–35. 39 indexed citations

Pastore, Matthew, et al.. (2010). A tale of two deletions: A report of two novel 20p13 → pter deletions. American Journal of Medical Genetics Part A. 152A(4). 1000–1007. 11 indexed citations

Varga, Liz, Matthew Pastore, Thomas W. Prior, Gail E. Herman, & Kim L. McBride. (2009). The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly. Genetics in Medicine. 11(2). 111–117. 219 indexed citations

Cunningham, David, et al.. (2009). Developmental expression pattern of the cholesterogenic enzyme NSDHL and negative selection of NSDHL-deficient cells in the heterozygous Bpa1H/+ mouse. Molecular Genetics and Metabolism. 98(4). 356–366. 13 indexed citations

Herman, Gail E., et al.. (2007). Genetic testing in autism: how much is enough?. Genetics in Medicine. 9(5). 268–274. 81 indexed citations

Herman, Gail E.. (2003). Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes. Human Molecular Genetics. 12(90001). 75R–88. 138 indexed citations

10.

Herman, Gail E., Richard I. Kelley, David Glenn Smith, et al.. (2002). Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome). Genetics in Medicine. 4(6). 434–438. 42 indexed citations

11.

Herman, Gail E., et al.. (2002). Characterization of mutations in fifty North American patients with X-linked myotubular myopathy. Human Mutation. 19(2). 114–121. 59 indexed citations

12.

Boyd, Yvonne, et al.. (1998). Mouse chromosome X. Mammalian Genome. 8(S1). S361–S377. 5 indexed citations

13.

Levin, Michael, Arnab Chatterjee, Antonella Pragliola, et al.. (1996). A comparative transcription map of the murine bare patches (Bpa) and striated (Str) critical regions and human Xq28.. Genome Research. 6(6). 465–477. 36 indexed citations

14.

Blair, Helen J., et al.. (1996). The Mouse X-Linked Developmental Mutant, Tattered, Lies betweenDXMit55andXkhand Is Associated with Hyperkeratinization. Genomics. 37(2). 238–241. 9 indexed citations

15.

Chatterjee, Arnab, Toshihiro Tanaka, Julia Parrish, & Gail E. Herman. (1995). Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X Chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions. Mammalian Genome. 6(11). 802–804. 10 indexed citations

16.

Gariboldi, Manuela, Elena Maestrini, Federico Canzian, et al.. (1994). Comparative Mapping of the Actin-Binding Protein 280 Genes in Human and Mouse. Genomics. 21(2). 428–430. 16 indexed citations

17.

Craigen, William J., Cornelis Jakobs, Elizabeth A. Sekul, et al.. (1994). d-2-Hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction. Pediatric Neurology. 10(1). 49–53. 26 indexed citations

18.

Brown, S.D.M., P. Avner, & Gail E. Herman. (1992). Mouse X Chromosome. Mammalian Genome. 3(S1). S274–S288. 12 indexed citations

19.

Arn, Pamela, Elizabeth R. Hauser, George H. Thomas, et al.. (1990). Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus. New England Journal of Medicine. 322(23). 1652–1655. 140 indexed citations

20.

Herman, Gail E., et al.. (1990). Close linkage of the murine locus bare patches to the X-linked visual pigment gene: Implications for mapping human X-linked dominant chondrodysplasia punctata. Genomics. 7(3). 307–312. 24 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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