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Joni L Rutter

Showing results (21-30 of 38) with videos related to

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JAMA|March 1, 2007
Genetic research and smoking behaviorLaura Jean Bierut, Joseph F Cubells, William G Iacono, et al.
Nature Reviews. Drug Discovery|February 6, 2024
The Bespoke Gene Therapy Consortium: facilitating development of AAV gene therapies for rare diseasesP J Brooks, Timothy M Miller, Frédéric Revah, et al.
Human Mutation|July 23, 2003
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individualsJoni L Rutter, Amelia M Smith, Michael R Dávila, et al.
Cancer|November 6, 2004
Heterogeneity of risk for melanoma and pancreatic and digestive malignancies: a melanoma case-control studyJoni L Rutter, Christina M Bromley, Alisa M Goldstein, et al.
Radiation Research|January 14, 2009
Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in KazakhstanAlice J Sigurdson, Charles E Land, Parveen Bhatti, et al.
Orphanet Journal of Rare Diseases|October 22, 2021
The IDeaS initiative: pilot study to assess the impact of rare diseases on patients and healthcare systemsAinslie Tisdale, Christine M Cutillo, Ramaa Nathan, et al.
Plos Medicine|August 3, 2018
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
Plos One|April 22, 2009
Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigmScott F Saccone, Laura J Bierut, Elissa J Chesler, et al.
Plos Medicine|August 17, 2018
Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
Plos One|July 2, 2020
Diversity and inclusion for the All of Us research program: A scoping reviewBrandy M Mapes, Christopher S Foster, Sheila V Kusnoor, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
JAMA|March 1, 2007
Genetic research and smoking behaviorLaura Jean Bierut, Joseph F Cubells, William G Iacono, et al.
Nature Reviews. Drug Discovery|February 6, 2024
The Bespoke Gene Therapy Consortium: facilitating development of AAV gene therapies for rare diseasesP J Brooks, Timothy M Miller, Frédéric Revah, et al.
Human Mutation|July 23, 2003
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individualsJoni L Rutter, Amelia M Smith, Michael R Dávila, et al.
Cancer|November 6, 2004
Heterogeneity of risk for melanoma and pancreatic and digestive malignancies: a melanoma case-control studyJoni L Rutter, Christina M Bromley, Alisa M Goldstein, et al.
Radiation Research|January 14, 2009
Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in KazakhstanAlice J Sigurdson, Charles E Land, Parveen Bhatti, et al.
Orphanet Journal of Rare Diseases|October 22, 2021
The IDeaS initiative: pilot study to assess the impact of rare diseases on patients and healthcare systemsAinslie Tisdale, Christine M Cutillo, Ramaa Nathan, et al.
Plos Medicine|August 3, 2018
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
Plos One|April 22, 2009
Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigmScott F Saccone, Laura J Bierut, Elissa J Chesler, et al.
Plos Medicine|August 17, 2018
Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
Plos One|July 2, 2020
Diversity and inclusion for the All of Us research program: A scoping reviewBrandy M Mapes, Christopher S Foster, Sheila V Kusnoor, et al.
Pageof 4