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Effect Modification by Social Determinants of Pharmacogenetic Medication Interactions on 90-Day Hospital Readmissions within an Integrated U.S. Healthcare System.
Published in:
Journal of Personalized Medicine, 2022, v. 12, n. 7, p. 1145, doi. 10.3390/jpm12071145
By:
- Saulsberry, Loren;
- Singh, Lavisha;
- Pruitt, Jaclyn;
- Ward, Christopher;
- Wake, Dyson T.;
- Gibbons, Robert D.;
- Meltzer, David O.;
- O'Donnell, Peter H.;
- Cruz-Knight, Wanda;
- Hulick, Peter J.;
- Dunnenberger, Henry M.;
- David, Sean P.
Publication type:
Article
Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment.
Published in:
Journal of Personalized Medicine, 2020, v. 10, n. 4, p. 165, doi. 10.3390/jpm10040165
By:
- Lemke, Amy A.;
- Amendola, Laura M.;
- Kuchta, Kristine;
- Dunnenberger, Henry M.;
- Thompson, Jennifer;
- Johnson, Christian;
- Ilbawi, Nadim;
- Oshman, Lauren;
- Hulick, Peter J.
Publication type:
Article
Utility of Polygenic Scores for Differentiating Diabetes Diagnosis Among Patients With Atypical Phenotypes of Diabetes.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 1, p. 107, doi. 10.1210/clinem/dgad456
By:
- Billings, Liana K;
- Shi, Zhuqing;
- Wei, Jun;
- Rifkin, Andrew S;
- Zheng, S Lilly;
- Helfand, Brian T;
- Ilbawi, Nadim;
- Dunnenberger, Henry M;
- Hulick, Peter J;
- Qamar, Arman;
- Xu, Jianfeng
Publication type:
Article
Flype: Software for enabling personalized medicine.
Published in:
American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2021, v. 187, n. 1, p. 37, doi. 10.1002/ajmg.c.31867
By:
- Helseth, Donald L.;
- Gulukota, Kamalakar;
- Miller, Nicholas;
- Yang, Mathew;
- Werth, Tom;
- Sabatini, Linda M.;
- Bouma, Mike;
- Dunnenberger, Henry M.;
- Wake, Dyson T.;
- Hulick, Peter J.;
- Kaul, Karen L.;
- Khandekar, Janaradan D.
Publication type:
Article
Implementation of a multidisciplinary pharmacogenomics clinic in a community health system.
Published in:
American Journal of Health-System Pharmacy, 2016, v. 73, n. 23, p. 1956, doi. 10.2146/ajhp160072
By:
- Dunnenberger, Henry M.;
- Biszewski, Matthew;
- Bell, Gillian C.;
- Sereika, Annette;
- May, Holley;
- Johnson, Samuel G.;
- Hulick, Peter J.;
- Khandekar, Janardan
Publication type:
Article
Hematologic toxicity in BRCA1 and BRCA2 mutation carriers during chemotherapy: A retrospective matched cohort study.
Published in:
Cancer Medicine, 2019, v. 8, n. 12, p. 5609, doi. 10.1002/cam4.2471
By:
- West, Allison H.;
- Knollman, Hayley;
- Dugan, James;
- Hedeker, Donald;
- Handorf, Elisabeth A.;
- Nielsen, Sarah M.;
- Bealin, Lisa C.;
- Goldblatt, Lindsay G.;
- Willems, Heather;
- Daly, Mary B.;
- Afghahi, Anosheh;
- Olopade, Olufunmilayo I.;
- Hulick, Peter J.;
- Shagisultanova, Elena;
- Huo, Dezheng;
- Obeid, Elias;
- Churpek, Jane E.
Publication type:
Article
Cystic fibrosis F508del carriers and cancer risk: Results from the UK Biobank.
Published in:
International Journal of Cancer, 2021, v. 148, n. 7, p. 1658, doi. 10.1002/ijc.33431
By:
- Shi, Zhuqing;
- Wei, Jun;
- Na, Rong;
- Resurreccion, W. Kyle;
- Zheng, S. Lilly;
- Hulick, Peter J.;
- Helfand, Brian T.;
- Talamonti, Mark S.;
- Xu, Jianfeng
Publication type:
Article
Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank.
Published in:
2020
By:
- Wei, Jun;
- Shi, Zhuqing;
- Na, Rong;
- Wang, Chi-Hsiung;
- Resurreccion, W. Kyle;
- Zheng, S. Lilly;
- Hulick, Peter J.;
- Cooney, Kathleen A.;
- Helfand, Brian T.;
- Isaacs, William B.;
- Xu, Jianfeng
Publication type:
journal article
Bernard-Soulier syndrome: Common ancestry in two African American families with the GP Ibα Leu129Pro mutation.
Published in:
American Journal of Hematology, 2000, v. 65, n. 2, p. 141, doi. 10.1002/1096-8652(200010)65:2<141::AID-AJH9>3.0.CO;2-H
By:
- Antonucci, John Vito;
- Martin, Eric S.;
- Hulick, Peter J.;
- Joseph, Abraham;
- Martin, S. Eric
Publication type:
Article
Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
Published in:
2021
By:
- Haverfield, Eden V.;
- Esplin, Edward D.;
- Aguilar, Sienna J.;
- Hatchell, Kathryn E.;
- Ormond, Kelly E.;
- Hanson-Kahn, Andrea;
- Atwal, Paldeep S.;
- Macklin-Mantia, Sarah;
- Hines, Stephanie;
- Sak, Caron W.-M.;
- Tucker, Steven;
- Bleyl, Steven B.;
- Hulick, Peter J.;
- Gordon, Ora K.;
- Velsher, Lea;
- Gu, Jessica Y. J.;
- Weissman, Scott M.;
- Kruisselbrink, Teresa;
- Abel, Christopher;
- Kettles, Michele
Publication type:
Journal Article
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
Published in:
BMC Medicine, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12916-021-01999-2
By:
- Haverfield, Eden V.;
- Esplin, Edward D.;
- Aguilar, Sienna J.;
- Hatchell, Kathryn E.;
- Ormond, Kelly E.;
- Hanson-Kahn, Andrea;
- Atwal, Paldeep S.;
- Macklin-Mantia, Sarah;
- Hines, Stephanie;
- Sak, Caron W.-M.;
- Tucker, Steven;
- Bleyl, Steven B.;
- Hulick, Peter J.;
- Gordon, Ora K.;
- Velsher, Lea;
- Gu, Jessica Y. J.;
- Weissman, Scott M.;
- Kruisselbrink, Teresa;
- Abel, Christopher;
- Kettles, Michele
Publication type:
Article
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
Published in:
BMC Medicine, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12916-021-01999-2
By:
- Haverfield, Eden V.;
- Esplin, Edward D.;
- Aguilar, Sienna J.;
- Hatchell, Kathryn E.;
- Ormond, Kelly E.;
- Hanson-Kahn, Andrea;
- Atwal, Paldeep S.;
- Macklin-Mantia, Sarah;
- Hines, Stephanie;
- Sak, Caron W.-M.;
- Tucker, Steven;
- Bleyl, Steven B.;
- Hulick, Peter J.;
- Gordon, Ora K.;
- Velsher, Lea;
- Gu, Jessica Y. J.;
- Weissman, Scott M.;
- Kruisselbrink, Teresa;
- Abel, Christopher;
- Kettles, Michele
Publication type:
Article
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
Published in:
2021
By:
- Haverfield, Eden V.;
- Esplin, Edward D.;
- Aguilar, Sienna J.;
- Hatchell, Kathryn E.;
- Ormond, Kelly E.;
- Hanson-Kahn, Andrea;
- Atwal, Paldeep S.;
- Macklin-Mantia, Sarah;
- Hines, Stephanie;
- Sak, Caron W.-M.;
- Tucker, Steven;
- Bleyl, Steven B.;
- Hulick, Peter J.;
- Gordon, Ora K.;
- Velsher, Lea;
- Gu, Jessica Y. J.;
- Weissman, Scott M.;
- Kruisselbrink, Teresa;
- Abel, Christopher;
- Kettles, Michele
Publication type:
journal article
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
Published in:
BMC Medicine, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12916-021-01999-2
By:
- Haverfield, Eden V.;
- Esplin, Edward D.;
- Aguilar, Sienna J.;
- Hatchell, Kathryn E.;
- Ormond, Kelly E.;
- Hanson-Kahn, Andrea;
- Atwal, Paldeep S.;
- Macklin-Mantia, Sarah;
- Hines, Stephanie;
- Sak, Caron W.-M.;
- Tucker, Steven;
- Bleyl, Steven B.;
- Hulick, Peter J.;
- Gordon, Ora K.;
- Velsher, Lea;
- Gu, Jessica Y. J.;
- Weissman, Scott M.;
- Kruisselbrink, Teresa;
- Abel, Christopher;
- Kettles, Michele
Publication type:
Article
Observed evidence for guideline‐recommended genes in predicting prostate cancer risk from a large population‐based cohort.
Published in:
Prostate, 2021, v. 81, n. 13, p. 1002, doi. 10.1002/pros.24195
By:
- Wei, Jun;
- Yang, Wancai;
- Shi, Zhuqing;
- Lu, Lucy;
- Wang, Qiang;
- Resurreccion, W. Kyle;
- Engelmann, Valentina;
- Zheng, S. Lilly;
- Hulick, Peter J.;
- Cooney, Kathleen A.;
- Isaacs, William B.;
- Helfand, Brian T.;
- Lu, Jim;
- Xu, Jianfeng
Publication type:
Article
BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry.
Published in:
Human Mutation, 2019, v. 40, n. 10, p. 1781, doi. 10.1002/humu.23804
By:
- Friebel, Tara M.;
- Andrulis, Irene L.;
- Balmaña, Judith;
- Blanco, Amie M.;
- Couch, Fergus J.;
- Daly, Mary B.;
- Domchek, Susan M.;
- Easton, Douglas F.;
- Foulkes, William D.;
- Ganz, Patricia A.;
- Garber, Judy;
- Glendon, Gord;
- Greene, Mark H.;
- Hulick, Peter J.;
- Isaacs, Claudine;
- Jankowitz, Rachel C.;
- Karlan, Beth Y.;
- Kirk, Judy;
- Kwong, Ava;
- Lee, Annette
Publication type:
Article
Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.
Published in:
Human Mutation, 2016, v. 37, n. 1, p. 84, doi. 10.1002/humu.22920
By:
- Capuano, Alessandra;
- Bucciotti, Francesco;
- Farwell, Kelly D.;
- Tippin Davis, Brigette;
- Mroske, Cameron;
- Hulick, Peter J.;
- Weissman, Scott M.;
- Gao, Qingshen;
- Spessotto, Paola;
- Colombatti, Alfonso;
- Doliana, Roberto
Publication type:
Article

Found: 17