Andrew K Sobering

13PUBLICATIONS
35CO-AUTHORS
NeonatologyCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Educational counsellingNeurology and neuromuscular diseases
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Publications (13)

|Apr 24, 2026
Clinical and Neurodevelopmental Course in a Case of EFNB1-Related Craniofrontonasal Syndrome With Unrepaired Craniosynostosis.

|Apr 29, 2025
Two New Cases Expand the Phenotypic Spectrum of TUBG1 Missense Variants.

Roser Urreizti, Jessica Vissicchio, Mohamed Idries

|Jul 15, 2024
Expanding the clinical phenotype and variant spectrum associated with RFX7.

Talia Sisroe, Attila Dos Santos, Alyssa L Rippert

|Oct 26, 2022
Teaching perspectives on the communication of difficult news of genetic conditions to medical students.

Ashley M Vanasse, Tracey Weiler, Elizabeth A Roth

|Sep 23, 2022
A novel SYNJ1 homozygous variant causing developmental and epileptic encephalopathy in an Afro-Caribbean individual.

Mary Maj, Christie L Taylor, Kevin Landau

|Feb 21, 2022
A novel unbalanced translocation between chromosomes 5p and 18q leading to dysmorphology and global developmental delay.

Giavanna Verdi, Dong Li, Sarah H Elsea

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Frequent Collaborators

6 joint publications

Elizabeth J Bhoj

3 joint publications

Dong Li

3 joint publications

Sarah H Elsea

3 joint publications

John C Carey