Laura Schoch Farach (Laura Farach, Laura S Farach)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 11

Top Topics

Genome Wide Association

Dna Methylation

Histone Deacetylase

Top Venues

American journal of medical genetics. Part A

Clinical case reports

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

Publications

Melissa A Richard, Philip J Lupo, Erik A Ehli, Mustafa Sahin, Darcy A Krueger, Joyce Y Wu, Elizabeth M Bebin, Kit Sing Au, Hope Northrup, Laura Schoch Farach, null null
Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. American journal of medical genetics. Part A 194 (6) (2024)
Melissa A Richard, Philip J Lupo, Erik A Ehli, Mustafa Sahin, Darcy A Krueger, Joyce Y Wu, Elizabeth M Bebin, Kit Sing Au, Hope Northrup, Laura Schoch Farach, null null
Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. American journal of medical genetics. Part A 194 (6) (2024)
Melissa A Richard, Philip J Lupo, Erik A Ehli, Mustafa Sahin, Darcy A Krueger, Joyce Y Wu, Elizabeth M Bebin, Kit Sing Au, Hope Northrup, Laura Schoch Farach, null null
Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. American journal of medical genetics. Part A 194 (6) (2024)
Melissa A Richard, Philip J Lupo, Erik A Ehli, Mustafa Sahin, Darcy A Krueger, Joyce Y Wu, Elizabeth M Bebin, Kit Sing Au, Hope Northrup, Laura Schoch Farach, null null
Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. American journal of medical genetics. Part A (2024)
Melissa A Richard, Philip J Lupo, Erik A Ehli, Mustafa Sahin, Darcy A Krueger, Joyce Y Wu, Elizabeth M Bebin, Kit Sing Au, Hope Northrup, Laura Schoch Farach, null null
Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. American journal of medical genetics. Part A 194 (6) (2024)
Melissa A Richard, Philip J Lupo, Erik A Ehli, Mustafa Sahin, Darcy A Krueger, Joyce Y Wu, Elizabeth M Bebin, Kit Sing Au, Hope Northrup, Laura Schoch Farach, null null
Common epilepsy variants from the general population are not associated with epilepsy among individuals with tuberous sclerosis complex. American journal of medical genetics. Part A 194 (6) (2024)
Abigail Kacpura, Marta Frigeni, Kathryn A Gunther, Laura Schoch Farach
Clinical and biochemical outcomes in cobalamin C deficiency with use of high-dose hydroxocobalamin in the early neonatal period. American journal of medical genetics. Part A 188 (6) (2022)
Kathryn A Gunther, Kate Mowrey, Laura Schoch Farach
Two new reported cases of 16q22.3q23.3 duplication syndrome highlight intrafamilial variability and potential sex expression differences within a rare duplication syndrome. Clinical case reports 9 (3) (2021)
Stephanie M Baskin, Shaine Alaine Morris, Autumn Vara, Jacqueline T Hecht, Laura Schoch Farach
The first reported case of Loeys-Dietz syndrome in a patient with biallelic SMAD3 variants. American journal of medical genetics. Part A 182 (11) (2020)
Victoria F Wagner, Paul R Hillman, Allison D Britt, Joseph W Ray, Laura Schoch Farach
A De novo HDAC2 variant in a patient with features consistent with Cornelia de Lange syndrome phenotype. American journal of medical genetics. Part A 179 (5) (2019)
Laura Schoch Farach, Mary E Little, Angela L Duker, Clare V Logan, Andrew Jackson, Jaqueline T Hecht, Michael Bober
The expanding phenotype of RNU4ATAC pathogenic variants to Lowry Wood syndrome. American journal of medical genetics. Part A 176 (2) (2017)