Michael H. Guo

Neurology

3400 Civic Center Boulevard
South Pavilion, 2nd Floor
Philadelphia, PA 19104

Last Updated: 09/26/2026

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Found 45 publications

Linking candidate causal autoimmune variants to T cell networks using genetic and epigenetic screens in primary human T cells.

Linking candidate causal autoimmune variants to T cell networks using genetic and epigenetic screens in primary human T cells.

Journal: bioRxiv : the preprint server for biology

Published: October 17, 2024

Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networks.

Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networks.

Journal: Nature genetics

Published: September 15, 2024

Ischemic stroke associated with amyloid-related imaging abnormalities in a patient treated with lecanemab.

Ischemic stroke associated with amyloid-related imaging abnormalities in a patient treated with lecanemab.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association

Published: July 02, 2024

Disparities in Genetic Testing for Neurologic Disorders.

Disparities in Genetic Testing for Neurologic Disorders.

Journal: Neurology

Published: March 06, 2024

The Importance of Offering Exome or Genome Sequencing in Adult Neuromuscular Clinics.

The Importance of Offering Exome or Genome Sequencing in Adult Neuromuscular Clinics.

Journal: Biology

Published: January 09, 2024

Polygenic burden of short tandem repeat expansions promote risk for Alzheimer's disease.

Polygenic burden of short tandem repeat expansions promote risk for Alzheimer's disease.

Journal: medRxiv : the preprint server for health sciences

Published: November 28, 2023

Polygenic burden of short tandem repeat expansions promotes risk for Alzheimer's disease.

Polygenic burden of short tandem repeat expansions promotes risk for Alzheimer's disease.

Journal: Nature communications

Published: November 16, 2023

Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts.

Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts.

Journal: Journal of neurology

Published: August 18, 2023

Inferring compound heterozygosity from large-scale exome sequencing data.

Inferring compound heterozygosity from large-scale exome sequencing data.

Journal: bioRxiv : the preprint server for biology

Published: March 30, 2023

Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG).

Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG).

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

Published: March 30, 2023

Inferring compound heterozygosity from large-scale exome sequencing data.

Inferring compound heterozygosity from large-scale exome sequencing data.

Journal: Nature genetics

Published: March 24, 2023

OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivity.

OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivity.

Journal: The Journal of clinical investigation

Published: May 13, 2022

Showing 1-12 of 45

Last Updated: 09/26/2026