Christina Tise

Assistant Professor

Stanford University School of Medicine

United States

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About

Christina Tise is an Assistant Professor at Stanford University School of Medicine in the United States. Her research primarily focuses on newborn screening, genetic disorders, and molecular testing, as evidenced by her recent publications on conditions such as X-Linked Adrenoleukodystrophy and Zellweger spectrum disorder. Additionally, she has investigated the implications of genetic variants and their diagnosis in both clinical and biochemical contexts.

Articles (13)

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2021

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2021

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2021

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2020

Collaborators (3)

Richard Chang

Associate Professor

University of California Irvine School of Medicine

UNITED STATES

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José Andrés Morales Corado

Assistant Professor

Columbia University Irving Medical Center

UNITED STATES

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Ethylin Jabs

Professor and Director of Center for Craniofacial Developmental and Disorders

Johns Hopkins University School of Medicine

UNITED STATES

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Christina Tise

Research Interests

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Articles (13)

Molecular testing in newborn screening: VUS burden among true positives and secondary reproductive limitations via expanded carrier screening panels

Newborn Screening for X-Linked Adrenoleukodystrophy (X-ALD): Biochemical, Molecular, and Clinical Characteristics of Other Genetic Conditions

Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome

A homozygous Gly470Ala variant in PEX6 causes severe Zellweger spectrum disorder

MT‐ATP6 mitochondrial disease identified by newborn screening reveals a distinct biochemical phenotype

Neonatal lupus is a novel cause of positive newborn screening for X‐linked adrenoleukodystrophy

Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel SLC6A8 Variant Causing a Treatable but Likely Underdiagnosed Genetic Disorder

Recent tPA administration can cause pseudo‐hyperargininemia and may mimic arginase deficiency or arginine supplementation

Short Bones, Renal Stones, and Diagnostic Moans: Hypercalcemia in a Girl Found to Have Coffin-Lowry Syndrome

Medical genetics training in the COVID‐19 era: A resident's perspective

Genetics of recurrent pregnancy loss: a review.

Aicardi-Goutières syndrome may present with positive newborn screen for X-linked adrenoleukodystrophy.

Case 1: Rapidly Rising Bilirubin Level in a 3-day-old Term Infant.

Collaborators (3)

Richard Chang

José Andrés Morales Corado

Ethylin Jabs

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