Kevin M. Bowling

7.2k total citations · 1 hit paper
24 papers, 1.4k citations indexed

About

Kevin M. Bowling is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Kevin M. Bowling has authored 24 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 9 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Kevin M. Bowling's work include Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (7 papers) and BRCA gene mutations in cancer (3 papers). Kevin M. Bowling is often cited by papers focused on Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (7 papers) and BRCA gene mutations in cancer (3 papers). Kevin M. Bowling collaborates with scholars based in United States, Mexico and France. Kevin M. Bowling's co-authors include R Myers, Jason Gertz, Katherine E. Varley, Timothy E. Reddy, Florencia Pauli, Stephanie Parker, Devin Absher, Marie K. Cross, J Stamatoyannopoulos and Gregory E. Crawford and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Kevin M. Bowling

21 papers receiving 1.3k 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.

Dynamic DNA methylation across diverse human cell lines and tissues

2013 512 citations Katherine E. Varley, Jason Gertz et al. Genome Research profile →

Peers

Countries citing papers authored by Kevin M. Bowling

Since Specialization

Citations

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

Fields of papers citing papers by Kevin M. Bowling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kevin M. Bowling. 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 Kevin M. Bowling. The network helps show where Kevin M. Bowling may publish in the future.

Co-authorship network of co-authors of Kevin M. Bowling

This figure shows the co-authorship network connecting the top 25 collaborators of Kevin M. Bowling. A scholar is included among the top collaborators of Kevin M. Bowling 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 Kevin M. Bowling. Kevin M. Bowling 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

#	Work	Indexed citations
1	Survey of Demographics, Training, Duties, and Professional Development for Variant Scientists in Genomic Medicine 2025 ·Journal of Molecular Diagnostics ·Alexa Dickson, (unknown), Barbara K. Fortini, Jennifer Goldstein, Michelle L. Thompson, (unknown), Anna Hurst, Molly C. Schroeder, Katarzyna Polonis, Kevin M. Bowling	0
2	Age, Sex, and Anatomical Location Patterns in Cutaneous Pyogenic Granuloma Cases 2025 ·JAMA Dermatology ·Umber Dube, (unknown), Kevin M. Bowling, Jonathan W. Heusel, Carrie C. Coughlin	0
3	Evaluating pathogenicity of variants of unknown significance in APP, PSEN1, and PSEN2 2025 ·Neurotherapeutics ·Jacob Marsh, Guangming Huang, Kevin M. Bowling, Alan E. Renton, (unknown), T. Blake Ball, Cyril Pottier, Carlos Cruchaga, Gregory S. Day, Randall J. Bateman, Jorge J. Llibre‐Guerra, Eric McDade, Celeste M. Karch	1
4	Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism 2024 ·Clinical Genetics ·(unknown), Kevin M. Bowling, Alexa Dickson, (unknown), Molly C. Schroeder, Julie Neidich, Jonathan W. Heusel, Kilannin Krysiak, Katarzyna Polonis, Bijal A. Parikh, (unknown)	3
5	Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations 2024 ·Clinical Genetics ·Reza Ghasemi, (unknown), Kevin M. Bowling, Kilannin Krysiak, Jason Walker, Alexa Dickson, Molly C. Schroeder, Bijal A. Parikh, Julie Neidich, Katarzyna Polonis, (unknown)	0
6	Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing 2023 ·Genetics in Medicine ·(unknown), James M.J. Lawlor, Susan M. Hiatt, Michelle L. Thompson, Donald R. Latner, Candice R. Finnila, Kevin M. Bowling, (unknown), (unknown), Nicole Kelly, Whitley V. Kelley, (unknown), (unknown), Melissa Kelly, Ghunwa Nakouzi, Laura G. Hendon, E. Martina Bebin, Eimear E. Kenny, Gregory M. Cooper	8
7	Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing 2022 ·Genome Medicine ·Kevin M. Bowling, Michelle L. Thompson, Melissa Kelly, Sarah Scollon, Anne Slavotinek, Bradford C. Powell, Brian Kirmse, Laura G. Hendon, Kyle B. Brothers, Bruce R. Korf, Gregory M. Cooper, John M. Greally, Anna Hurst	10
8	Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders 2021 ·SHILAP Revista de lepidopterología ·Susan M. Hiatt, James M.J. Lawlor, Lori H. Handley, Ryne C. Ramaker, Brianne B. Rogers, E. Christopher Partridge, Lori Beth Boston, Melissa Williams, Christopher Plott, Jerry Jenkins, Stacy W. Gray, James Holt, Kevin M. Bowling, E. Martina Bebin, Jane Grimwood, Jeremy Schmutz, Gregory M. Cooper	30
9	Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls 2020 ·Genetics in Medicine ·Kevin M. Bowling, Michelle L. Thompson, Stacy W. Gray, James M.J. Lawlor, Kelly L. Williams, Kelly M. East, Whitley V. Kelley, (unknown), Devin Absher, E. Christopher Partridge, Anna Hurst, Jeffrey C. Edberg, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper	9
10	Fibulin-5 mutation featuring Charcot-Marie-Tooth disease, joint hyperlaxity, and scoliosis 2020 ·Neurology Genetics ·Mohamed Kazamel, Michael A. Lopez, Martina Bebin, Kevin M. Bowling, Bruce R. Korf, Gregory S. Barsh, Gregory M. Cooper, Anna Hurst, Eroboghene E. Ubogu	1
11	Complexities of genetic diagnosis illustrated by an atypical case of congenital hypoplastic anemia 2018 ·Molecular Case Studies ·David Claassen, (unknown), Kevin M. Bowling, Gregory M. Cooper, (unknown), Michael S. Hershfield, Sara Lewis, (unknown), Mitchell J. Weiss, Jeremie H. Estepp	10
12	Genomic sequencing identifies secondary findings in a cohort of parent study participants 2018 ·Genetics in Medicine ·Michelle L. Thompson, Candice R. Finnila, Kevin M. Bowling, Kyle B. Brothers, Matthew B. Neu, Michelle D. Amaral, Susan M. Hiatt, Kelly M. East, Stacy W. Gray, James M.J. Lawlor, Whitley V. Kelley, Edward J. Lose, Carla A. Rich, Shirley Simmons, Shawn Levy, R Myers, Gregory S. Barsh, E. Martina Bebin, Gregory M. Cooper	19
13	Post-mortem molecular profiling of three psychiatric disorders 2017 ·Genome Medicine ·Ryne C. Ramaker, Kevin M. Bowling, Brittany N. Lasseigne, Megan Hastings Hagenauer, Andrew A. Hardigan, Nicholas S. Davis, Jason Gertz, Preston Cartagena, David Walsh, Marquis P. Vawter, Edward G. Jones, Alan F. Schatzberg, Jack D. Barchas, Stanley J. Watson, Blynn G. Bunney, Huda Akil, William E. Bunney, Jun Z. Li, Sara J. Cooper, R Myers	132
14	Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results 2016 ·Genetics in Medicine ·Kyle B. Brothers, Kelly M. East, Whitley V. Kelley, (unknown), (unknown), Carla A. Rich, Kevin M. Bowling, Edward J. Lose, E. Martina Bebin, Shirley Simmons, John Myers, Gregory S. Barsh, R Myers, Gregory M. Cooper, Jill M. Pulley, Mark A. Rothstein, Ellen Wright Clayton	29
15	Recurrent read-through fusion transcripts in breast cancer 2014 ·Breast Cancer Research and Treatment ·Katherine E. Varley, Jason Gertz, Brian S. Roberts, Nicholas S. Davis, Kevin M. Bowling, Marie K. Kirby, (unknown), Patsy G. Oliver, William E. Grizzle, Andres Forero, Donald J. Buchsbaum, Albert F. LoBuglio, R Myers	128
16	Dynamic DNA methylation across diverse human cell lines and tissues breakdown → 2013 ·Genome Research ·Katherine E. Varley, Jason Gertz, Kevin M. Bowling, Stephanie Parker, Timothy E. Reddy, Florencia Pauli, Marie K. Cross, Brian A. Williams, J Stamatoyannopoulos, Gregory E. Crawford, Devin Absher, B Wold, R Myers	512
17	Analysis of DNA Methylation in a Three-Generation Family Reveals Widespread Genetic Influence on Epigenetic Regulation 2011 ·PLoS Genetics ·Jason Gertz, Katherine E. Varley, Timothy E. Reddy, Kevin M. Bowling, Florencia Pauli, Stephanie Parker, Katerina S. Kucera, Huntington F. Willard, R Myers	213
18	Direct Binding of GTP Cyclohydrolase and Tyrosine Hydroxylase 2008 ·Journal of Biological Chemistry ·Kevin M. Bowling, Zhinong Huang, Dong Xu, (unknown), Christopher D. Funderburk, (unknown), Wendi S. Neckameyer, Janis M. O’Donnell	36
19	Interaction of Genetic and Environmental Factors in aDrosophilaParkinsonism Model 2007 ·Journal of Neuroscience ·Anathbandhu Chaudhuri, Kevin M. Bowling, Christopher D. Funderburk, Hakeem O. Lawal, Arati A. Inamdar, Zhe Wang, Janis M. O’Donnell	155
20	A typical N-terminal Extensions Confer Novel Regulatory Properties on GTP Cyclohydrolase Isoforms in Drosophila melanogaster 2006 ·Journal of Biological Chemistry ·Christopher D. Funderburk, Kevin M. Bowling, Dong Xu, Zhinong Huang, Janis M. O’Donnell	22

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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