Sara S. Ellingwood

Sara S. Ellingwood

Allergy and Immunology

7500 Challis Rd
Entrance 1, Level 2
Brighton, MI 48116

Last Updated: 09/26/2026

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Found 10 publications

Effect of Gender and Special Considerations for Women in Mastocytosis and Anaphylaxis.

Effect of Gender and Special Considerations for Women in Mastocytosis and Anaphylaxis.

Journal: Immunology and allergy clinics of North America

Published: September 27, 2023

Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.

Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.

Journal: Science advances

Published: May 01, 2023

Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.

Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.

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

Published: October 20, 2021

BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy.

BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy.

Journal: EMBO molecular medicine

Published: December 04, 2020

A DNA repair disorder caused by de novo monoallelic DDB1 variants is associated with a neurodevelopmental syndrome.

A DNA repair disorder caused by de novo monoallelic DDB1 variants is associated with a neurodevelopmental syndrome.

Journal: American journal of human genetics

Published: October 26, 2020

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.

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

Published: July 24, 2020

De novo substitutions of TRPM3 cause intellectual disability and epilepsy.

De novo substitutions of TRPM3 cause intellectual disability and epilepsy.

Journal: European journal of human genetics : EJHG

Published: January 18, 2019

Biochemical and clinical aspects of glycogen storage diseases.

Biochemical and clinical aspects of glycogen storage diseases.

Journal: The Journal of endocrinology

Published: May 24, 2018

SYT1-associated neurodevelopmental disorder: a case series.

SYT1-associated neurodevelopmental disorder: a case series.

Journal: Brain : a journal of neurology

Published: November 02, 2017

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations.

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations.

Journal: American journal of human genetics

Published: July 27, 2015

Showing 1-10 of 10

Last Updated: 09/26/2026