Haley Streff

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Poornima L Tamma, Haley Streff, Chaya N Murali
A novel de novo pathogenic variant in TBL1XR1 as a new proposed cause of Pierpont syndrome. American journal of medical genetics. Part A (2023)
Poornima L Tamma, Haley Streff, Chaya N Murali
A novel de novo pathogenic variant in TBL1XR1 as a new proposed cause of Pierpont syndrome. American journal of medical genetics. Part A (2023)
Sujal Manohar, Yoel Gofin, Haley Streff, Liesbeth Vossaert, Pamela Camacho, Chaya N Murali
A familial deletion of 10p12.1 associated with thrombocytopenia. American journal of medical genetics. Part A (2023)
Hadley Stevens Smith, Rachel Franciskovich, Andrea M Lewis, Amanda Gerard, Rebecca O Littlejohn, Kimberly Nugent, Janah Rodriguez, Haley Streff
Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics. Genetics in medicine : official journal of the American College of Medical Genetics 23 (5) (2021)
Tiana M Scott, Hui Guo, Evan E Eichler, Jill Anne Rosenfeld, Kaifang Pang, Zhandong Liu, Seema Lalani, Weimin Bi, Yaping Yang, Carlos A Bacino, Haley Streff, Andrea M Lewis, Mary K Koenig, Isabelle Thiffault, Allison Bellomo, David B Everman, Julie R Jones, Roger E Stevenson, Raphael Bernier, Christian Gilissen, Rolph Pfundt, Susan M Hiatt, Gregory M Cooper, Jimmy L Holder, Daryl A Scott
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder. Human mutation 41 (5) (2020)