1. Matching Two Independent Cohorts Validates DPH1 as a Gene Responsible for Autosomal Recessive Intellectual Disability with Short Stature, Craniofacial, and Ectodermal Anomalies. Issue 10 (17th August 2015) Authors: Loucks, Catrina M.; Parboosingh, Jillian S.; Shaheen, Ranad; Bernier, Francois P.; McLeod, D. Ross; Seidahmed, Mohammed Z.; Puffenberger, Erik G.; Ober, Carole; Hegele, Robert A.; Boycott, Kym M.; Alkuraya, Fowzan S.; Innes, A. Micheil Journal: Human mutation Issue: Volume 36:Issue 10(2015:Oct.) Page Start: 1015 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Patient‐specific genetic factors predict treatment failure in sofosbuvir‐treated patients with chronic hepatitis C. (21st February 2022) Authors: Loucks, Catrina M.; Lin, Jennifer J.; Trueman, Jessica N.; Drögemöller, Britt I.; Wright, Galen E. B.; Chang, Wan‐Chun; Li, Kathy H.; Yoshida, Eric M.; Ford, Jo‐Ann; Lee, Samuel S.; Crotty, Pam; Kim, Richard B.; Al‐Judaibi, Bandar; Schwarz, Ute I.; Ramji, Alnoor; Farivar, Jeanette F.; Tam, Edward... Journal: Liver international Issue: Volume 42:Number 4(2022) Page Start: 796 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Pharmacogenetic testing to guide therapeutic decision‐making and improve outcomes for children undergoing anthracycline‐based chemotherapy. (11th May 2021) Authors: Loucks, Catrina M.; Yan, Kevin; Tanoshima, Reo; Ross, Colin J. D.; Rassekh, Shahrad R.; Carleton, Bruce C. Other Names: Pottegård Anton guestEditor.; Stage Tore B. guestEditor. Journal: Basic & clinical pharmacology & toxicology Issue: Volume 130:Supplement 1(2022) Page Start: 95 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗