Suchergebnisse - "Ahimaz, Priyanka"

PubPharm (22)

1

Genetic counselors' utilization of ChatGPT in professional practice : A cross-sectional study

enthalten in: American journal of medical genetics. Part A | 2024

von Ahimaz, P. | Bergner, A. | Florido, M. | +2

2

Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine

enthalten in: American journal of medical genetics. Part A | 2024

von Freiman, A. | Rekab, A. | Bergner, A. | +3

3

Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics

enthalten in: Journal of genetic counseling | 2024

von Cheung, C. | Berger, S. | Ross, M. | +7

4

Future Frontiers : Exploration of practices, challenges, and educational needs of genetic counselors in emerging subspecialties

enthalten in: Journal of genetic counseling | 2023

von Ahimaz, P. | Ross, M. | Foltz, J. | +5

5

Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays

enthalten in: European journal of human genetics : EJHG | 2023

von Ganapathi, M. | Matsuoka, L. | March, M. | +35

6

Exploring the role of genetic counselors in immunology : A study of immunologist and allergist perspectives

enthalten in: The journal of allergy and clinical immunology. In practice | 2023

von Ahimaz, P. | Foltz, J. | Ross, M. | +3

7

Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von van Jaarsveld, R. | Reilly, J. | Cornips, M. | +56

8

A novel biallelic loss-of-function variant in DAND5 causes heterotaxy syndrome

enthalten in: Cold Spring Harbor molecular case studies | 2022

von Ganapathi, M. | Buchovecky, C. | Cristo, F. | +7

9

Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers-Danlos syndrome

enthalten in: American journal of medical genetics. Part A | 2022

von Ahimaz, P. | Kramer, T. | Swaroop, P. | +4

10

Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas

enthalten in: HGG advances | 2022

von Zhong, G. | Ahimaz, P. | Edwards, N. | +15

ErratumIn: HGG Adv. 2022 Jun 29;3(3):100126. - PMID 35800210