Suchergebnisse - "Ahimaz, Priyanka"

PubPharm (40)

21

Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID-19 pandemic

enthalten in: Journal of genetic counseling | 2021

von Ma, D. | Ahimaz, P. | Mirocha, J. | +4

22

A novel homozygous variant in TRAPPC2L results in a neurodevelopmental disorder and disrupts TRAPP complex function

enthalten in: Journal of medical genetics | 2021

von Al-Deri, N. | Okur, V. | Ahimaz, P. | +7

23

COVID contingencies : Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies

enthalten in: Journal of genetic counseling | 2021

von Ahimaz, P. | Giordano, J. | Disco, M. | +7

24

Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics : A Study of Parents and Adolescents

enthalten in: Circulation. Genomic and precision medicine | 2021

von Ahimaz, P. | Sabatello, M. | Qian, M. | +15

25

Novel candidate genes in esophageal atresia/tracheoesophageal fistula identified by exome sequencing

enthalten in: European journal of human genetics : EJHG | 2021

von Wang, J. | Ahimaz, P. | Hashemifar, S. | +7

26

COVID contingencies : Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies

enthalten in: Journal of Genetic Counseling | 2021

von Ahimaz, P. | Giordano, J. | Disco, M. | +7

27

Clinical genetic counselor experience in the adoption of telehealth in the United States and Canada during the COVID‐19 pandemic

enthalten in: Journal of Genetic Counseling | 2021

von Ma, D. | Ahimaz, P. | Mirocha, J. | +4

28

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis

enthalten in: Human genetics | 2020

von Ganapathi, M. | Argyriou, L. | Martínez-Azorín, F. | +21

29

COVID-19's Impact on Genetics at One Medical Center in New York

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2020

von Pereira, E. | Columbia University Clinical Genetics Professionals | Chung, W. | +33

30

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis

enthalten in: Human genetics | 2020

von Ganapathi, M. | Argyriou, L. | Martínez-Azorín, F. | +21