Lina Gonzalez

7PUBLICATIONS
2CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesGlycoconjugates
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Publications (7)

|Aug 20, 2026
The SMYD1 p.Asn101Ser is a partial loss-of-function variant that impairs mitochondrial function and leads to early-onset cardiomyopathy.

|Mar 08, 2026
Unusual Recombinant Chromosome 6 Derived From a Parental Rearrangement With Complex Paracentric Inversions.

Melanie Babcock, Marwa Daghsni, Jessica Sebastian

|Jan 22, 2025
Genomic sequencing: the case for equity of care in the era of personalized medicine.

Lina Ghaloul-Gonzalez, Lisa S Parker, Jonathan M Davis

|Apr 18, 2024
Clinical case report of intractable paroxysmal sympathetic hyperactivity in TANGO2 deficiency disorder.

Kaitlin Morrison, Hitoshi Koshiya, Robert Safier

|May 05, 2021
Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach.

Rachel M Wolfe, Al-Walid Mohsen, Cate Walsh Vockley

|Apr 05, 2021
Under-referral of Plain community members for genetic services despite being qualified for genetic evaluation.

Sarah Ehrenberg, Catherine Walsh Vockley, Erica Nelson

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Frequent Collaborators

1 joint publications

Svetlana A Yatsenko

1 joint publications

Marta W Szulik