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K

Kathryn E. Hatchell

University of California System

17H-index
83Paper Count
1.2KCitation Count
Published Papers 30
Publication Date
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Using patient-reported outcomes from the PROCLAIM trial to assess the impact of universal germline genetic testing for prostate cancer patients
errProstate Cancer and Prostatic Diseases
IF5.8
err2025-09-22
err0
errOAAI
errNeal D. Shore; Christopher M. Pieczonka; Sean Heron; Mukaram Gazi; David J. Cahn; Laurence H. Belkoff; Aaron D. Berger; Brian Mazzarella; Joseph Veys; David Morris; Richard Bevan-Thomas; Alexander Engelman; Paul Dato; David R. Wise; Mary Kay Hardwick; Kerry W. Aradhya; Brandie Heald; Robert L. Nussbaum; Kathryn E. Hatchell; Brianna Bucknor; Edward D. Esplin; Sarah M. Nielsen
errShare
errSave
Experience using conventional compared to ancestry-based population descriptors in clinical genomics laboratories
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2025-01-01
err1
errOAAI
errHatchell, Kathryn E.; Poll, Sarah R.; Russell, Emily M.; Williams, Trevor J.; Ellsworth, Rachel E.; Facio, Flavia M.; Aguilar, Sienna; Esplin, Edward D.; Popejoy, Alice B.; Nussbaum, Robert L.; Aradhya, Swaroop
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errSave
Clinician-Reported Management Recommendations in Response to Universal Germline Genetic Testing in Patients With Prostate Cancer
errJOURNAL OF UROLOGY
IF6.8
err2024-12-01
err3
PREAI
errShore, Neal; Pieczonka, Christopher; Heron, Sean; Gazi, Mukaram; Cahn, David; Belkoff, Laurence H.; Berger, Aaron; Mazzarella, Brian; Veys, Joseph; Idom, Charles; Morris, David; Jayram, Gautam; Engelman, Alexander; Dato, Paul; Bevan-Thomas, Richard; Wise, David R.; Hardwick, Mary Kay; Rojahn, Susan; Layman, Paige; Heald, Brandie; Ellsworth, Rachel E.; Hatchell, Kathryn E.; Nussbaum, Robert L.; Nielsen, Sarah M.; Esplin, Edward D.
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errSave
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy
errJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
IF3.2
err2024-08-14
err0
errOAAI
errRoggenbuck, Jennifer; Morales, Ana; Ellis, Colin A.; Dratch, Laynie; Stetler, Molly; Tan, Christopher A.; Bucknor, Brianna; Hatchell, Kathryn E.; Aradhya, Swaroop; Esplin, Edward D.; Ting, Yi-Lee; Scherer, Steven S.
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errSave
Real-World Genetic Testing Utilization Among Patients With Cardiomyopathy
errCIRCULATION-GENOMIC AND PRECISION MEDICINE
IF5.5
err2024-02-01
err1
PREAI
errMorales, Ana; Moretz, Chad; Ren, Sheng; Smith, Elizabeth; Callis, Thomas E.; Hall, Taryn; Hatchell, Kathryn E.; Nussbaum, Robert L.; Regalado, Ellen; Rojahn, Susan; Vatta, Matteo; Esplin, Edward D.; Murillo, Jaime
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The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change
errGENETICS IN MEDICINE
IF6.2
err2023-12-01
err36
errOAAI
errRehm, Heidi L.; Alaimo, Joseph T.; Aradhya, Swaroop; Bayrak-Toydemir, Pinar; Best, Hunter; Brandon, Rhonda; Buchan, Jillian G.; Chao, Elizabeth C.; Chen, Elaine; Clifford, Jacob; Cohen, Ana S. A.; Conlin, Laura K.; Das, Soma; Davis, Kyle W.; del Gaudio, Daniela; Del Viso, Florencia; Divincenzo, Christina; Eisenberg, Marcia; Guidugli, Lucia; Hammer, Monia B.; Harrison, Steven M.; Hatchell, Kathryn E.; Dyer, Lindsay Havens; Hoang, Lily U.; Holt, James M.; Jobanputra, Vaidehi; Karbassi, Izabela D.; Kearney, Hutton M.; Kelly, Melissa A.; Kelly, Jacob M.; Kluge, Michelle L.; Komala, Timothy; Kruszka, Paul; Lau, Lynette; Lebo, Matthew S.; Marshall, Christian R.; Mcknight, Dianalee; Mcwalter, Kirsty; Meng, Yan; Nagan, Narasimhan; Neckelmann, Christian S.; Neerman, Nir; Niu, Zhiyv; Paolillo, Vitoria K.; Paolucci, Sarah A.; Perry, Denise; Pesaran, Tina; Radtke, Kelly; Rasmussen, Kristen J.; Retterer, Kyle; Saunders, Carol J.; Spiteri, Elizabeth; Stanley, Christine; Szuto, Anna; Taft, Ryan J.; Thiffault, Isabelle; Thomas, Brittany C.; Thomas-Wilson, Amanda; Thorpe, Erin; Tidwell, Timothy J.; Towne, Meghan C.; Zouk, Hana
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errSave
Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing
errJAMA NETWORK OPEN
IF9.7
err2023-10-25
err43
errOAAI
errChen, Elaine; Facio, Flavia M.; Aradhya, Kerry W.; Rojahn, Susan; Hatchell, Kathryn E.; Aguilar, Sienna; Ouyang, Karen; Saitta, Sulagna; Hanson-Kwan, Andrea K.; Capurro, Nicole Nakousi; Takamine, Eriko; Jamuar, Saumya Shekhar; McKnight, Dianalee; Johnson, Britt; Aradhya, Swaroop
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errSave
Testing and Management of Iron Overload After Genetic Screening-Identified Hemochromatosis
errJAMA NETWORK OPEN
IF9.7
err2023-10-23
err6
errOAAI
errSavatt, Juliann M.; Johns, Alicia; Schwartz, Marci L. B.; McDonald, Whitney S.; Salvati, Zachary M.; Oritz, Nicole M.; Masnick, Max; Hatchell, Kathryn; Hao, Jing; Buchanan, Adam H.; Williams, Marc S.
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errSave
Efficacy of National Comprehensive Cancer Network Guidelines in Identifying Pathogenic Germline Variants Among Unselected Patients with Prostate Cancer: The PROCLAIM Trial
errEUROPEAN UROLOGY ONCOLOGY
IF9.3
err2023-10-01
err8
errOAAI
errShore, Neal; Gazi, Mukaram; Pieczonka, Christopher; Heron, Sean; Modh, Rishi; Cahn, David; Belkoff, Laurence H.; Berger, Aaron; Mazzarella, Brian; Veys, Joseph; Idom, Charles; Morris, David; Jayram, Gautam; Engelman, Alexander; Bukkapatnam, Raviender; Dato, Paul; Bevan-Thomas, Richard; Cornell, Robert; Wise, David R.; Hardwick, Mary Kay; Hernandez, Ryan D.; Rojahn, Susan; Layman, Paige; Hatchell, Kathryn E.; Heald, Brandie; Nussbaum, Robert L.; Nielsen, Sarah M.; Esplin, Edward D.
errShare
errSave
Racial disparities in cascade testing for cancer predisposition genes
errPREVENTIVE MEDICINE
IF3.2
err2023-07-01
err9
PREAI
errKassem, Nawal M.; Althouse, Sandra K.; Monahan, Patrick O.; Hayes, Lisa; Nielsen, Sarah M.; Heald, Brandie; Esplin, Edward D.; Hatchell, Kathryn E.; Ballinger, Tarah J.
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errSave
Comparison of Germline Genetic Testing Before and After a Medical Policy Covering Universal Testing Among Patients With Colorectal Cancer
errJAMA NETWORK OPEN
IF9.7
err2022-10-24
err9
errOAAI
errMoretz, Chad; Byfield, Stacey DaCosta; Hatchell, Kathryn E.; Dalton, Joline; Onglao, Peter Nicholas; Hang, Lillian; Hansen, Pamela; Radford, Cristi; Nielsen, Sarah M.; Heald, Brandie; Munro, Sandra B.; Nussbaum, Robert L.; Esplin, Edward D.
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Cancer risks associated with heterozygous ATM loss of function and missense pathogenic variants based on multigene panel analysis
errBREAST CANCER RESEARCH AND TREATMENT
IF3
err2022-09-12
err6
PREAI
errLaitman, Yael; Nielsen, Sarah M.; Bernstein-Molho, Rinat; Heald, Brandie; Hatchell, Kathryn E.; Esplin, Edward D.; Friedman, Eitan
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errSave
Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing
errJAMA CARDIOLOGY
IF14.1
err2022-09-01
err34
errOAAI
errDellefave-Castillo, Lisa M.; Cirino, Allison L.; Callis, Thomas E.; Esplin, Edward D.; Garcia, John; Hatchell, Kathryn E.; Johnson, Britt; Morales, Ana; Regalado, Ellen; Rojahn, Susan; Vatta, Matteo; Nussbaum, Robert L.; McNally, Elizabeth M.
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errSave
Germline Pathogenic Variant Prevalence Among Latin American and US Hispanic Individuals Undergoing Testing for Hereditary Breast and Ovarian Cancer: A Cross-Sectional Study
errJCO GLOBAL ONCOLOGY
IF3
err2022-07-01
err13
errOAAI
errOssa Gomez, Carlos Andres; Achatz, Maria Isabel; Hurtado, Mabel; Sanabria-Salas, Maria Carolina; Sullcahuaman, Yasser; Chavarri-Guerra, Yanin; Dutil, Julie; Nielsen, Sarah M.; Esplin, Edward D.; Michalski, Scott T.; Bristow, Sara L.; Hatchell, Kathryn E.; Nussbaum, Robert L.; Pineda-Alvarez, Daniel E.; Ashton-Prolla, Patricia
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errSave
Germline alterations among Hispanic men with prostate cancer (April, 10.1038/s41391-022-00539-0, 2022)
errPROSTATE CANCER AND PROSTATIC DISEASES
IF5.8
err2022-04-29
err1
errOAAI
errPan, Elizabeth; Shaya, Justin; Madlensky, Lisa; Randall, J. Michael; Javier-Desloges, Juan; Millard, Frederick E.; Rose, Brent; Parsons, J. Kellogg; Nielsen, Sarah M.; Hatchell, Kathryn E.; Esplin, Edward D.; Nussbaum, Robert L.; Weise, Nicole; Murphy, James; Martinez, Maria Elena; McKay, Rana R.
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errSave
Clinical validation of genomic functional screen data: Analysis of observed BRCA1 variants in an unselected population cohort
errHUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
err2022-04-01
err5
errOAAI
errBarrett, Kelly M. Schiabor; Masnick, Max; Hatchell, Kathryn E.; Savatt, Juliann M.; Banet, Natalie; Buchanan, Adam; Willard, Huntington F.
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errSave
The impact of proband indication for genetic testing on the uptake of cascade testing among relatives
errGENETICS IN MEDICINE
IF6.2
err2022-03-01
err0
errOAAI
errSchmidlen, Tara; Hatchell, Kathryn; Bristow, Sara L.; Haverfield, Eden
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errSave
Germline alterations among Hispanic men with prostate cancer
errPROSTATE CANCER AND PROSTATIC DISEASES
IF5.8
err2022-02-28
err6
PREAI
errPan, Elizabeth; Shaya, Justin; Madlensky, Lisa; Randall, J. Michael; Millard, Frederick E.; Rose, Brent; Parsons, J. Kellogg; Nielsen, Sarah M.; Hatchell, Kathryn E.; Esplin, Edward D.; Nussbaum, Robert L.; Weise, Nicole; Murphy, James; Martinez, Maria Elena; Mckay, Rana R.
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errSave
CDH1 germline variants are enriched in patients with colorectal cancer, gastric cancer, and breast cancer
errBRITISH JOURNAL OF CANCER
IF6.8
err2021-12-23
err19
errOAAI
errAdib, Elio; El Zarif, Talal; Nassar, Amin H.; Akl, Elie W.; Abou Alaiwi, Sarah; Mouhieddine, Tarek H.; Esplin, Edward D.; Hatchell, Kathryn; Nielsen, Sarah M.; Rana, Huma Q.; Choueiri, Toni K.; Kwiatkowski, David J.; Sonpavde, Guru
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errSave
Hereditary Cancer Risk Using a Genetic Chatbot Before Routine Care Visits
errOBSTETRICS AND GYNECOLOGY
IF4.7
err2021-11-04
err50
errOAAI
errNazareth, Shivani; Hayward, Laura; Simmons, Emilie; Snir, Moran; Hatchell, Kathryn E.; Rojahn, Susan; Slotnick, Robert Nathan; Nussbaum, Robert L.
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Research Directions

No research directions
Co-authors
Cooperation Journals
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Eric Boerwinkle
H-index: 215 · Papers: 2.0K
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Bruce M. Psaty
H-index: 207 · Papers: 1.8K
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Jerome I. Rotter
H-index: 176 · Papers: 1.8K
R
Ruth J. F. Loos
H-index: 171 · Papers: 1.2K
T
Tamara B. Harris
H-index: 168 · Papers: 905
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