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Christine Kobelka

Showing results (1-10 of 11) with videos related to

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Prenatal Diagnosis|February 27, 2009
An evaluation of the decision-making process regarding amniocentesis following a screen-positive maternal serum screen resultChristine Kobelka, André Mattman, Sylvie Langlois
Gynecologic Oncology|June 5, 2019
Clinical characteristics and outcomes in elderly women with BRCA1 and BRCA2 mutationsChelsea Salyer, Christine Kobelka, Allison Barrie, et al.
NEJM Evidence|October 28, 2025
Direct-to-Consumer Genetic TestingJulianne M O'Daniel, Christine Kobelka, Kimberly Foss, et al.
Familial Cancer|February 9, 2010
Assessment of clinical practices among cancer genetic counselorsDeborah Wham, Thuy Vu, Gayun Chan-Smutko, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality|June 12, 2021
Electronic Family History Screening Tool for Detection of Inherited Cancer Risk: A Prospective Pilot StudyAmy Le, Emily Valice, Christine Kobelka, et al.
Clinical Genetics|December 20, 2021
Factors influencing genetic counseling and testing for hereditary breast and ovarian cancer syndrome in a large US health care systemC Bethan Powell, Cecile Laurent, Christine Garcia, et al.
Gynecologic Oncology|October 11, 2022
Management of ovarian and breast cancer risk in non-BRCA HBOC pathogenic variant carriers in a large California health care systemC Bethan Powell, Cecile Laurent, Christine Garcia, et al.
Gynecologic Oncology|August 12, 2020
Streamlining genetic testing for women with ovarian cancer in a Northern California health care systemC Bethan Powell, Cecile Laurent, Giuseppe Ciaravino, et al.
Prenatal Diagnosis|July 7, 2015
Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomaliesChristina L Alamillo, Zöe Powis, Kelly Farwell, et al.
Nature Genetics|December 24, 2013
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomasArkadiusz Piotrowski, Jing Xie, Ying F Liu, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Prenatal Diagnosis|February 27, 2009
An evaluation of the decision-making process regarding amniocentesis following a screen-positive maternal serum screen resultChristine Kobelka, André Mattman, Sylvie Langlois
Gynecologic Oncology|June 5, 2019
Clinical characteristics and outcomes in elderly women with BRCA1 and BRCA2 mutationsChelsea Salyer, Christine Kobelka, Allison Barrie, et al.
NEJM Evidence|October 28, 2025
Direct-to-Consumer Genetic TestingJulianne M O'Daniel, Christine Kobelka, Kimberly Foss, et al.
Familial Cancer|February 9, 2010
Assessment of clinical practices among cancer genetic counselorsDeborah Wham, Thuy Vu, Gayun Chan-Smutko, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality|June 12, 2021
Electronic Family History Screening Tool for Detection of Inherited Cancer Risk: A Prospective Pilot StudyAmy Le, Emily Valice, Christine Kobelka, et al.
Clinical Genetics|December 20, 2021
Factors influencing genetic counseling and testing for hereditary breast and ovarian cancer syndrome in a large US health care systemC Bethan Powell, Cecile Laurent, Christine Garcia, et al.
Gynecologic Oncology|October 11, 2022
Management of ovarian and breast cancer risk in non-BRCA HBOC pathogenic variant carriers in a large California health care systemC Bethan Powell, Cecile Laurent, Christine Garcia, et al.
Gynecologic Oncology|August 12, 2020
Streamlining genetic testing for women with ovarian cancer in a Northern California health care systemC Bethan Powell, Cecile Laurent, Giuseppe Ciaravino, et al.
Prenatal Diagnosis|July 7, 2015
Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomaliesChristina L Alamillo, Zöe Powis, Kelly Farwell, et al.
Nature Genetics|December 24, 2013
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomasArkadiusz Piotrowski, Jing Xie, Ying F Liu, et al.
Pageof 2