Christina G Tise (Christina G Perry)

ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 15

Top Venues

American journal of medical genetics. Part A

Journal of investigative medicine high impact case reports

JIMD reports

G3 (Bethesda, Md.)

Stanford Hospital and Clinics

Virginia Polytechnic Institute and State University (BSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Stanford Hospital and Clinics

United States

Resident Physician :: Medical Genetics

Education History

Virginia Polytechnic Institute and State University

United States

BSC :: Biochemistry

Publications

Christina G Tise, Melinda J Palma, Kristina P Cusmano-Ozog, Dena R Matalon
Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel SLC6A8 Variant Causing a Treatable but Likely Underdiagnosed Genetic Disorder. Journal of investigative medicine high impact case reports 11 (2023)
Christina G Tise, Courtney P Verscaj, Bryce A Mendelsohn, Jeremy Woods, Chung U Lee, Gregory M Enns, Zinandré Stander, Patricia L Hall, Tina M Cowan, Kristina P Cusmano-Ozog
MT-ATP6 mitochondrial disease identified by newborn screening reveals a distinct biochemical phenotype. American journal of medical genetics. Part A (2023)
Carolina I Galarreta, Karen Wong, Jason Carmichael, Jeremy Woods, Christina G Tise, Annie D Niehaus, Alison J Schildt, Courtney P Verscaj, Kristina P Cusmano-Ozog
A homozygous Gly470Ala variant in PEX6 causes severe Zellweger spectrum disorder. American journal of medical genetics. Part A (2023)
Christina G Tise, Courtney P Verscaj, Bryce A Mendelsohn, Jeremy Woods, Chung U Lee, Gregory M Enns, Zinandré Stander, Patricia L Hall, Tina M Cowan, Kristina P Cusmano-Ozog
MT-ATP6 mitochondrial disease identified by newborn screening reveals a distinct biochemical phenotype. American journal of medical genetics. Part A (2023)
Christina G Tise, Melinda J Palma, Kristina P Cusmano-Ozog, Dena R Matalon
Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel SLC6A8 Variant Causing a Treatable but Likely Underdiagnosed Genetic Disorder. Journal of investigative medicine high impact case reports 11 (2023)
Christina G Tise, Melinda J Palma, Kristina P Cusmano-Ozog, Dena R Matalon
Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel SLC6A8 Variant Causing a Treatable but Likely Underdiagnosed Genetic Disorder. Journal of investigative medicine high impact case reports 11 (2023)
Christina G Tise, Melinda J Palma, Kristina P Cusmano-Ozog, Dena R Matalon
Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel SLC6A8 Variant Causing a Treatable but Likely Underdiagnosed Genetic Disorder. Journal of investigative medicine high impact case reports 11 (2023)
Annie D Niehaus, Bryce A Mendelsohn, Bree Zimmerman, Chung U Lee, Melanie A Manning, Kristina P Cusmano-Ozog, Christina G Tise
Neonatal lupus is a novel cause of positive newborn screening for X-linked adrenoleukodystrophy. American journal of medical genetics. Part A (2023)
Ryan W Gates, Susanna Balcells, David A Stevenson, Ethylin Wang Jabs, Colette DeFilippo, Maura R Z Ruzhnikov, Christina G Tise
Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome. American journal of medical genetics. Part A (2023)
Kristina P Cusmano-Ozog, Alicia K Renck, Christina G Tise
Recent tPA administration can cause pseudo-hyperargininemia and may mimic arginase deficiency or arginine supplementation. JIMD reports 63 (6) (2022)
Christina G Tise, Dena R Matalon, Melanie A Manning, Heather M Byers, Monica Grover
Short Bones, Renal Stones, and Diagnostic Moans: Hypercalcemia in a Girl Found to Have Coffin-Lowry Syndrome. Journal of investigative medicine high impact case reports 10 (2022)
Christina G Tise
Medical genetics training in the COVID-19 era: A resident's perspective. American journal of medical genetics. Part A 185 (10) (2021)
Christina G Tise, Jose Andres Morales, Ariel S Lee, Frances Velez-Bartolomei, Brendan J Floyd, Rebecca J Levy, Kristina P Cusmano-Ozog, Annette S Feigenbaum, Maura R Z Ruzhnikov, Chung U Lee, Gregory M Enns
Aicardi-Goutières syndrome may present with positive newborn screen for X-linked adrenoleukodystrophy. American journal of medical genetics. Part A 185 (6) (2021)
Christina G Tise, James A Perry, Leslie E Anforth, Mary A Pavlovich, Joshua D Backman, Kathleen A Ryan, Joshua P Lewis, Jeffrey R O'Connell, Laura M Yerges-Armstrong, Alan R Shuldiner
From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases. G3 (Bethesda, Md.) 6 (9) (2016)
Christina G Tise, Katherine G Holmes, Ann L Gruber-Baldini, Karen E Anderson, Lisa M Shulman, William J Weiner, Stephen G Reich
Are Patients with Psychogenic Movement Disorders More Likely to be Healthcare Workers? Movement disorders clinical practice 4 (1) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Christina G Tise (Christina G Perry)