Priyanka Ahimaz

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 9

Top Topics

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

Journal of genetic counseling

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Priyanka Ahimaz, Meredith Ross, Jennah Foltz, Monisha Sebastin, Ketki Naik, Tamar Kramer, Kelsie Bogyo, Michelle Primiano
Future Frontiers: Exploration of practices, challenges, and educational needs of genetic counselors in emerging subspecialties. Journal of genetic counseling (2023)
Andrew Freiman, Aisha Rekab, Amanda L Bergner, Elaine Maria Pereira, Yuhuan Lin, Priyanka Ahimaz
Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine. American journal of medical genetics. Part A 194 (4) (2023)
Andrew Freiman, Aisha Rekab, Amanda L Bergner, Elaine Maria Pereira, Yuhuan Lin, Priyanka Ahimaz
Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine. American journal of medical genetics. Part A (2023)
Andrew Freiman, Aisha Rekab, Amanda L Bergner, Elaine Maria Pereira, Yuhuan Lin, Priyanka Ahimaz
Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine. American journal of medical genetics. Part A 194 (4) (2023)
Priyanka Ahimaz, Amanda L Bergner, Michelle E Florido, Nina Harkavy, Sriya Bhattacharyya
Genetic counselors' utilization of ChatGPT in professional practice: A cross-sectional study. American journal of medical genetics. Part A (2023)
Andrew Freiman, Aisha Rekab, Amanda L Bergner, Elaine Maria Pereira, Yuhuan Lin, Priyanka Ahimaz
Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine. American journal of medical genetics. Part A 194 (4) (2023)
Mythily Ganapathi, Leticia S Matsuoka, Michael March, Dong Li, Elly Brokamp, Sara Benito-Sanz, Susan M White, Katherine Lachlan, Priyanka Ahimaz, Anshuman Sewda, Lisa Bastarache, Amanda Thomas-Wilson, Joan M Stoler, Nuria C Bramswig, Júlia Baptista, Karen L Stals, Florence Demurger, Benjamin Cogné, Bertrand Isidor, Maria Francesca Bedeschi, Angela Peron, Jeanne Amiel, Elaine H Zackai, John P Schacht, Alejandro D Iglesias, Jenny Morton, Ariane Schmetz, null null, Verónica Seidel, Stephanie Lucia, Stephanie M Baskin, Isabelle Thiffault, Joy D Cogan, Christopher T Gordon, Wendy K Chung, Sarah Bowdin, Elizabeth Joyce Bhoj
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. European journal of human genetics : EJHG (2023)
Priyanka Ahimaz, Tamar Kramer, Pooja Swaroop, McKenzie Mitchell, Rebecca Hernan, Kwame Anyane-Yeboa, Elaine Maria Pereira
Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers-Danlos syndrome. American journal of medical genetics. Part A 188 (11) (2022)
Priyanka Ahimaz, Jessica Giordano, Michele Disco, Elizabeth Harrington, Elana Levinson, Erica Spiegel, Carli Andrews, Emily Griffin, Rebecca Hernan, Julia Wynn
COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies. Journal of genetic counseling 30 (4) (2021)