Haley Streff

5PUBLICATIONS
75CO-AUTHORS
Central nervous systemEpigenetics (incl. genome methylation and epigenomics)Gene mappingInfant and child healthDevelopmental genetics (incl. sex determination)
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Publications (5)

|Oct 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC.

Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan

|Sep 25, 2023
A familial deletion of 10p12.1 associated with thrombocytopenia.

Sujal Manohar, Yoel Gofin, Haley Streff

|Feb 27, 2023
A novel de novo pathogenic variant in TBL1XR1 as a new proposed cause of Pierpont syndrome.

Poornima L Tamma, Haley Streff, Chaya N Murali

|Jan 21, 2021
Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics.

Hadley Stevens Smith, Rachel Franciskovich, Andrea M Lewis

|Jan 31, 2020
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder.

Tiana M Scott, Hui Guo, Evan E Eichler

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Frequent Collaborators

2 joint publications

Chaya N Murali

1 joint publications

Tiana M Scott

1 joint publications

Hui Guo

1 joint publications

Jill A Rosenfeld