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Kevin M. Bowling

washington university (wustl)

30H-index
131Paper Count
7.2KCitation Count
Published Papers 38
Publication Date
Developing a genetic return of results service core
err2025-11-17
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errMckenzie, Jennifer A.; Mcroy, Erin; Bowling, Kevin M.; De Luque, Jorge Luis Granadillo; Mozersky, Jessica; Linnenbringer, Erin; Baldridge, Dustin; Heusel, Jonathan W.; Neidich, Julie A.; Cashen, Amanda F.; Bierut, Laura J.; Hartz, Sarah M.; Gurnett, Christina A.
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High depth targeted next-generation sequencing in vascular malformations
err2025-11-01
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PREAI
errPakhathirathien, Pattima; Wongkittichote, Parith; Wittayakornrerk, Sanchawan; Treesit, Tharintorn; Feinggumloon, Sasikorn; Pichipichatkul, Kaewpitcha; Bua-Ngam, Chinnarat; Sarovath, Ajchariya; Thanachatchairattana, Pornsri; Dumrongwongsiri, Sarayuth; Bowling, Kevin M.; Corliss, Meagan M.; Cao, Yang; Tim-Aroon, Thipwimol; Khongkraparn, Arthaporn; Noojaroen, Saisuda; Wattanasirichaigoon, Duangrurdee
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Survey of Demographics, Training, Duties, and Professional Development for Variant Scientists in Genomic Medicine
err2025-07-22
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errOAAI
errAlexa Dickson; Kelsey R. Cone; Barbara K. Fortini; Jennifer Goldstein; Michelle L. Thompson; Matheus V.M.B. Wilke; Anna C.E. Hurst; Molly C. Schroeder; Katarzyna Polonis; Kevin M. Bowling
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Evaluating pathogenicity of variants of unknown significance in APP, PSEN1, and PSEN2
err2025-01-01
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errOAAI
errMarsh, Jacob A.; Huang, Guangming; Bowling, Kevin; Renton, Alan E.; Ziegemeier, Ellen; Ball, Torri; Pottier, Cyril; Cruchaga, Carlos; Day, Gregory S.; Bateman, Randall J.; Llibre-Guerra, Jorge J.; McDade, Eric
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Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing
err2023-08-01
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errOAAI
errFelker, Stephanie A.; Lawlor, James M. J.; Hiatt, Susan M.; Thompson, Michelle L.; Latner, Donald R.; Finnila, Candice R.; Bowling, Kevin M.; Bonnstetter, Zachary T.; Bonini, Katherine E.; Kelly, Nicole R.; V. Kelley, Whitley; Hurst, Anna C. E.; Rashid, Salman; Kelly, Melissa A.; Nakouzi, Ghunwa; Hendon, Laura G.; Bebin, E. Martina; Kenny, Eimear E.; Cooper, Gregory M.
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Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
err2023-06-21
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errOAAI
errLemke, Amy A.; Thompson, Michelle L.; Gimpel, Emily C.; McNamara, Katelyn C.; Rich, Carla A.; Finnila, Candice R.; Cochran, Meagan E.; Lawlor, James M. J.; East, Kelly M.; Bowling, Kevin M.; Latner, Donald R.; Hiatt, Susan M.; Amaral, Michelle D.; Kelley, Whitley V.; Greve, Veronica; Gray, David E.; Felker, Stephanie A.; Meddaugh, Hannah; Cannon, Ashley; Luedecke, Amanda; Jackson, Kelly E.; Hendon, Laura G.; Janani, Hillary M.; Johnston, Marla; Merin, Lee Ann; Deans, Sarah L.; Tuura, Carly; Hughes, Trent; Williams, Heather; Laborde, Kelly; Neu, Matthew B.; Patrick-Esteve, Jessica; Hurst, Anna C. E.; Kirmse, Brian M.; Savich, Renate; Spedale, Steven B.; Knight, Sara J.; Barsh, Gregory S.; Korf, Bruce R.; Cooper, Gregory M.; Brothers, Kyle B.
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Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing
err2022-11-21
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errOAAI
errBowling, Kevin M.; Thompson, Michelle L.; Kelly, Melissa A.; Scollon, Sarah; Slavotinek, Anne M.; Powell, Bradford C.; Kirmse, Brian M.; Hendon, Laura G.; Brothers, Kyle B.; Korf, Bruce R.; Cooper, Gregory M.; Greally, John M.; Hurst, Anna C. E.
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Genome sequencing as a first-line diagnostic test for hospitalized infants
err2022-04-01
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errBowling, Kevin M.; Thompson, Michelle L.; Finnila, Candice R.; Hiatt, Susan M.; Latner, Donald R.; Amaral, Michelle D.; Lawlor, James M. J.; East, Kelly M.; Cochran, Meagan E.; Greve, Veronica; Kelley, Whitley, V; Gray, David E.; Felker, Stephanie A.; Meddaugh, Hannah; Cannon, Ashley; Luedecke, Amanda; Jackson, Kelly E.; Hendon, Laura G.; Janani, Hillary M.; Johnston, Marla; Merin, Lee Ann; Deans, Sarah L.; Tuura, Carly; Williams, Heather; Laborde, Kelly; Neu, Matthew B.; Patrick-Esteve, Jessica; Hurst, Anna C. E.; Kandasamy, Jegen; Carlo, Wally; Brothers, Kyle B.; Kirmse, Brian M.; Savich, Renate; Superneau, Duane; Spedale, Steven B.; Knight, Sara J.; Barsh, Gregory S.; Korf, Bruce R.; Cooper, Gregory M.
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Parental impact of genome sequencing during the neonatal period
err2022-03-01
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errOAAI
errBrothers, Kyle; Rich, Carla; Gimpel, Emily; East, Kelly; Cochran, Meagan; Greve, Veronica; Kelley, Whitley V.; Jackson, Kelly; Hendon, Laura; Luedecke, Amanda; Janani, Hillary; Meddaugh, Hannah; Latner, Donald; Bowling, Kevin; Thompson, Michelle; Finnila, Candice; Hiatt, Susan; Amaral, Michelle; Lawlor, James; Gray, David; Felker, Stephanie; Cannon, Ashley; Johnston, Marla; Merin, Lee Ann; Deans, Sarah; Tuura, Carly; Williams, Heather; Laborde, Kelly; Neu, Matthew; Patrick-Esteve, Jessica; Hurst, Anna; Kandasamy, Jegen; Carlo, Waldemar; Kirmse, Brian; Savich, Renate; Superneau, Duane; Spedale, Steven; Knight, Sara; Barsh, Gregory; Korf, Bruce; Cooper, Gregory
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Integration of genomics into primary care via the Alabama Genomic Health Initiative
err2022-03-01
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errOAAI
errKorf, Bruce; Absher, Devin; Asif, Irfan; Bateman, Lori; Barsh, Gregory; Bowling, Kevin; Cooper, Gregory; Davis, Brittney; East, Kelly; Finnila, Candice; Goff, Blake; Kelly, Melissa; Kelley, Whitley; Latner, Donald; Lawlor, James; Limdi, Nita; May, Thomas; Might, Matthew; Moss, Irene; Nakano, Mariko; Osborne, Tiffany; Sodeke, Stephen; Stout, Adriana; Thompson, Michelle
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The clinical significance of poisoned splicing variants in early-onset neurodevelopmental disorders
err2022-03-01
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errOAAI
errFelker, Stephanie; Lawlor, James; Latner, Donald; Thompson, Michelle; Bowling, Kevin; Hiatt, Susan; Finnila, Candice; Cooper, Gregory
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Expansion of long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders and multiple congenital anomalies
err2022-03-01
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errOAAI
errHiatt, Susan; Lawlor, James; Handley, Lori; Bonnstetter, Zachary; Jenkins, Jerry; Lovell, John; Holt, James; Finnila, Candice; Thompson, Michelle; Latner, Donald; Partridge, Christopher; Plott, Christopher; Boston, Lori Beth; Williams, Melissa; Bowling, Kevin; Grimwood, Jane; Schmutz, Jeremy; Cooper, Gregory
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SouthSeq: Genome sequencing for a diverse population of hospitalized infants
err2022-03-01
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errOAAI
errLatner, Donald; Bowling, Kevin; Thompson, Michelle; Finnila, Candice; Hiatt, Susan; Amaral, Michelle; Lawlor, James; East, Kelly; Cochran, Meagan; Greve, Veronica; Kelley, Whitley V.; Gray, David; Felker, Stephanie; Meddaugh, Hannah; Cannon, Ashley; Luedecke, Amanda; Jackson, Kelly; Hendon, Laura; Janani, Hillary; Johnston, Marla; Merin, Lee Ann; Deans, Sarah; Tuura, Carly; Williams, Heather; Laborde, Kelly; Neu, Matthew; Patrick-Esteve, Jessica; Hurst, Anna; Kandasamy, Jegen; Carlo, Waldemar; Brothers, Kyle; Kirmse, Brian; Savich, Renate; Superneau, Duane; Spedale, Steven; Knight, Sara; Barsh, Gregory; Korf, Bruce; Cooper, Gregory
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A state-based approach to genomics for rare disease and population screening
err2021-04-01
err22
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errEast, Kelly M.; Kelley, Whitley V.; Cannon, Ashley; Cochran, Meagan E.; Moss, Irene P.; May, Thomas; Nakano-Okuno, Mariko; Sodeke, Stephen O.; Edberg, Jeffrey C.; Cimino, James J.; Fouad, Mona; Curry, William A.; Hurst, Anna C. E.; Bowling, Kevin M.; Thompson, Michelle L.; Bebin, E. Martina; Johnson, Robert D.; Acemgil, Aras; Acemgil, Aras; Crossman, David K.; Finnila, Candice R.; Gray, David E.; Greve, Veronica; Hardy, Sharonda; Hiatt, Susan M.; Latner, Donald R.; Lawlor, James M. J.; Miskell, Edrika L.; Narmore, Whitney; Schach, Julie H.; Cooper, Gregory M.; Might, Matthew; Barsh, Gregory S.; Korf, Bruce R.
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Long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders
err2021-04-01
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errHiatt, Susan M.; Lawlor, James M. J.; Handley, Lori H.; Ramaker, Ryne C.; Rogers, Brianne B.; Partridge, E. Christopher; Boston, Lori Beth; Williams, Melissa; Plott, Christopher B.; Jenkins, Jerry; Gray, David E.; Holt, James M.; Bowling, Kevin M.; Bebin, E. Martina; Grimwood, Jane; Schmutz, Jeremy; Cooper, Gregory M.
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Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls
err2021-02-01
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errOAAI
errBowling, Kevin M.; Thompson, Michelle L.; Gray, David E.; Lawlor, James M. J.; Williams, Kelly; East, Kelly M.; Kelley, Whitley V.; Moss, Irene P.; Absher, Devin M.; Partridge, E. Christopher; Hurst, Anna C. E.; Edberg, Jeffrey C.; Barsh, Gregory S.; Korf, Bruce R.; Cooper, Gregory M.
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Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies
err2020-11-01
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errAmendola, Laura M.; Muenzen, Kathleen; Biesecker, Leslie G.; Bowling, Kevin M.; Cooper, Greg M.; Dorschner, Michael O.; Driscoll, Catherine; Foreman, Ann Katherine M.; Golden-Grant, Katie; Greally, John M.; Hindorff, Lucia; Kanavy, Dona; Jobanputra, Vaidehi; Johnston, Jennifer J.; Kenny, Eimear E.; McNulty, Shannon; Murali, Priyanka; Ou, Jeffrey; Powell, Bradford C.; Rehm, Heidi L.; Rolf, Bradley; Roman, Tamara S.; Van Ziffle, Jessica; Guha, Saurav; Abhyankar, Avinash; Crosslin, David; Venner, Eric; Yuan, Bo; Zouk, Hana; Jarvik, Gail P.
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Fibulin-5 mutation featuring Charcot-Marie-Tooth disease, joint hyperlaxity, and scoliosis
err2020-08-01
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errOAAI
errKazamel, Mohamed; Lopez, Michael A.; Bebin, Martina; Bowling, Kevin; Korf, Bruce R.; Barsh, Gregory S.; Cooper, Gregory M.; Hurst, Anna C. E.; Ubogu, Eroboghene E.
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Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature
err2019-09-01
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errTorti, Erin; Keren, Boris; Palmer, Elizabeth E.; Zhu, Zehua; Afenjar, Alexandra; Anderson, Ilse J.; Andrews, Marisa, V; Atkinson, Celia; Au, Margaret; Berry, Susan A.; Bowling, Kevin M.; Boyle, Jackie; Buratti, Julien; Cathey, Sara S.; Charles, Perrine; Cogne, Benjamin; Courtin, Thomas; Escobar, Luis F.; Finley, Sabra Ledare; Graham, John M., Jr.; Grange, Dorothy K.; Heron, Delphine; Hewson, Stacy; Hiatt, Susan M.; Hibbs, Kathleen A.; Jayakar, Parul; Kalsner, Louisa; Larcher, Lise; Lesca, Gaetan; Mark, Paul R.; Miller, Kathryn; Nava, Caroline; Nizon, Mathilde; Pai, G. Shashidhar; Pappas, John; Parsons, Gretchen; Payne, Katelyn; Putoux, Audrey; Rabin, Rachel; Sabatier, Isabelle; Shinawi, Marwan; Shur, Natasha; Skinner, Steven A.; Valence, Stephanie; Warren, Hannah; Whalen, Sandra; Crunk, Amy; Douglas, Ganka; Monaghan, Kristin G.; Person, Richard E.; Willaert, Rebecca; Solomon, Benjamin D.; Juusola, Jane
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