Robert L Nussbaum (Sara L Bristow)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 13

Top Topics

Postoperative Pain

Clinical Decision Support

Top Venues

Journal of personalized medicine

JCO precision oncology

Circulation. Genomic and precision medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Steven Mark Sorscher, Jaclyn LoPiccolo, Brandie H Leach, Elaine Chen, Robert L Nussbaum, Scott T Michalski, Sarah M Nielsen, Alix M B Lacoste, Emil Keyder, Hayan Lee, Robert Luke Nussbaum, Renato G Martins, Edward D Esplin
Rate of Pathogenic Germline Variants in Patients With Lung Cancer. JCO precision oncology 7 (2023)
Carlos Andrés Ossa Gomez, Maria Isabel Waddington Achatz, Mabel Hurtado, María Carolina Sanabria-Salas, Yasser Sullcahuaman, Yanin Chávarri-Guerra, Julie Dutil, Sarah M Nielsen, Edward D Esplin, Scott T Michalski, Robert L Nussbaum, Kathryn E Hatchell, Robert Luke Nussbaum, Daniel E Pineda-Alvarez, Patricia Ashton-Prolla
Germline Pathogenic Variant Prevalence Among Latin American and US Hispanic Individuals Undergoing Testing for Hereditary Breast and Ovarian Cancer: A Cross-Sectional Study. JCO global oncology 8 (2022)
Kristine C Ashcraft, Kendra Grande, Robert L Nussbaum, Nicolas Moyer, Tara Schmidlen, Chad Moretz, Jennifer A Wick, Burns C Blaxall
Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug-Gene, Drug-Drug-Gene, and Drug-Gene-Gene Interaction Risks in a Large Patient Population. Journal of personalized medicine 12 (12) (2022)
Fernanda Leal-Pardinas, Rebecca Truty, Dianalee A McKnight, Britt Johnson, Ana Morales, Robert L Nussbaum, Tiffany Yar Pang, Jessica Cohen-Pfeffer, Emanuela Izzo, Raman Sankar, Sookyong Koh, Elaine C Wirrell, John J Millichap, Swaroop Aradhya
Value of genetic testing for pediatric epilepsy: Driving earlier diagnosis of ceroid lipofuscinosis type 2 Batten disease. Epilepsia 63 (7) (2022)
Kristine C Ashcraft, Kendra Grande, Robert L Nussbaum, Nicolas Moyer, Tara Schmidlen, Chad Moretz, Jennifer A Wick, Burns C Blaxall
Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug-Gene, Drug-Drug-Gene, and Drug-Gene-Gene Interaction Risks in a Large Patient Population. Journal of personalized medicine 12 (12) (2022)
Kristine C Ashcraft, Kendra Grande, Robert L Nussbaum, Nicolas Moyer, Tara Schmidlen, Chad Moretz, Jennifer A Wick, Burns C Blaxall
Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug-Gene, Drug-Drug-Gene, and Drug-Gene-Gene Interaction Risks in a Large Patient Population. Journal of personalized medicine 12 (12) (2022)
Kristine C Ashcraft, Kendra Grande, Robert L Nussbaum, Nicolas Moyer, Tara Schmidlen, Chad Moretz, Jennifer A Wick, Burns C Blaxall
Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug-Gene, Drug-Drug-Gene, and Drug-Gene-Gene Interaction Risks in a Large Patient Population. Journal of personalized medicine 12 (12) (2022)
Edward D Esplin, Sarah M Nielsen, Robert L Nussbaum, Judy E Garber, Heather Hampel, Huma Q Rana, N Jewel Samadder, Neal D Shore, Robert Luke Nussbaum
Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer. JCO precision oncology 6 (2022)
Whitney F Espinel, Marjan Champine, Heather Hampel, Joanne Jeter, Kevin Sweet, Robert Pilarski, Rachel Pearlman, Kate Shane, Pamela Brock, Judith A Westman, Lindsay Kipnis, Jilliane Sotelo, Anu Chittenden, Samantha Culver, Jill E Stopfer, Katherine A Schneider, Rosalba Sacca, Diane R Koeller, Shraddha Gaonkar, Erica Vaccari, Sarah Kane, Scott T Michalski, Shan Yang, Sarah M Nielsen, Robert L Nussbaum, Stephen E Lincoln, Robert L Nussbaum, Edward D Esplin
Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients. Cancers 14 (10) (2022)
Keith Nykamp, Rebecca Truty, Darlene Riethmaier, Julia Wilkinson, Robert L Nussbaum, Sienna Aguilar, Dana Neitzel, Nicole Faulkner, Swaroop Aradhya
Elucidating clinical phenotypic variability associated with the polyT tract and TG repeats in CFTR. Human mutation 42 (9) (2021)
Barry H Trachtenberg, Sachin K Shah, Robert L Nussbaum, Ruthvik Malladi, Matteo Vatta
Presence of the V122I Variant of Hereditary Transthyretin-Mediated Amyloidosis Among Self-Reported White Individuals in a Sponsored Genetic Testing Program. Circulation. Genomic and precision medicine 14 (5) (2021)
Eric T Rush, Britt Johnson, Swaroop Aradhya, Daniel Beltran, Robert L Nussbaum, Scott Eisenbeis, Norma E Guerra, Stan Krolczyk, Nicole Miller, Ana Morales, Prameela Ramesan, Soodabeh Sarafrazi, Rebecca Truty, Kathryn Dahir
Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2021)
Moran Snir, Shivani Nazareth, Emilie Simmons, Laura Hayward, Kristine Ashcraft, Robert L Nussbaum, Edward D Esplin, Swaroop Aradhya
Democratizing genomics: Leveraging software to make genetics an integral part of routine care. American journal of medical genetics. Part C, Seminars in medical genetics 187 (1) (2020)