Yevgeniya Svyryd

Tlalpan, DIF 14080, Mexico

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Breakpoint-resolved balanced t(2;12)(q35;q24.31) disrupting HNF1A in multigenerational MODY-3: Diagnostic utility of long-read genome sequencing and therapeutic impact.

Breakpoint-resolved balanced t(2;12)(q35;q24.31) disrupting HNF1A in multigenerational MODY-3: Diagnostic utility of long-read genome sequencing and therapeutic impact.

Journal: Metabolism open

Published: October 01, 2025

Solid pseudopapillary tumor of the pancreas: Clinical, histopathological, and molecular findings in a cohort of Mexican patients.

Solid pseudopapillary tumor of the pancreas: Clinical, histopathological, and molecular findings in a cohort of Mexican patients.

Journal: Revista de gastroenterologia de Mexico (English)

Published: February 27, 2025

Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency.

Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency.

Journal: Research square

Published: July 23, 2024

Molecular and Clinical Characterization of a Founder Mutation Causing G6PC3 Deficiency.

Molecular and Clinical Characterization of a Founder Mutation Causing G6PC3 Deficiency.

Journal: Journal of clinical immunology

Published: June 17, 2024

Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency.

Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency.

Journal: medRxiv : the preprint server for health sciences

Published: May 27, 2024

Bayesian polygenic risk estimation approach to nuclear families with discordant sib-pairs for myelomeningocele.

Bayesian polygenic risk estimation approach to nuclear families with discordant sib-pairs for myelomeningocele.

Journal: PloS one

Published: May 03, 2024

Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population.

Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population.

Journal: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion

Published: December 22, 2022

Telomeres Length Variations in a Rheumatoid Arthritis Patients Cohort at Early Disease Onset and after Follow-Up.

Telomeres Length Variations in a Rheumatoid Arthritis Patients Cohort at Early Disease Onset and after Follow-Up.

Journal: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion

Published: September 10, 2022

PPP2R2B hypermethylation causes acquired apoptosis deficiency in systemic autoimmune diseases.

PPP2R2B hypermethylation causes acquired apoptosis deficiency in systemic autoimmune diseases.

Journal: JCI insight

Published: July 24, 2019

Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans.

Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans.

Journal: Scientific reports

Published: September 14, 2018

Using Genetic and Epigenetic Markers to Improve Differential Diagnosis of Prostate Cancer and Benign Prostatic Hyperplasia by Noninvasive Methods in Mexican Patients.

Using Genetic and Epigenetic Markers to Improve Differential Diagnosis of Prostate Cancer and Benign Prostatic Hyperplasia by Noninvasive Methods in Mexican Patients.

Journal: Clinical genitourinary cancer

Published: November 10, 2017

Clinical and Genetic Findings in Mexican Patients with Duane Anomaly and Radial Ray Malformations/Okihiro Syndrome.

Clinical and Genetic Findings in Mexican Patients with Duane Anomaly and Radial Ray Malformations/Okihiro Syndrome.

Journal: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion

Published: December 13, 2016

Showing 1-12 of 15

Last Updated: 09/26/2026