Maria C. Manotas

Bogota, DC, Colombia

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications

Building a hereditary cancer program in Colombia: analysis of germline pathogenic and likely pathogenic variants spectrum in a high-risk cohort.

Building a hereditary cancer program in Colombia: analysis of germline pathogenic and likely pathogenic variants spectrum in a high-risk cohort.

Journal: European journal of human genetics : EJHG
Published: July 05, 2024

Epigenetic control of SOX9 gene by the histone acetyltransferase P300 in human Sertoli cells.

Epigenetic control of SOX9 gene by the histone acetyltransferase P300 in human Sertoli cells.

Journal: Heliyon
Published: January 01, 2024

SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas.

SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas.

Journal: Frontiers in genetics
Published: July 20, 2022

Variant curation and interpretation in hereditary cancer genes: An institutional experience in Latin America.

Variant curation and interpretation in hereditary cancer genes: An institutional experience in Latin America.

Journal: Molecular genetics & genomic medicine
Published: July 18, 2022

Preimplantation genetic testing in assisted reproduction.

Preimplantation genetic testing in assisted reproduction.

Journal: Minerva obstetrics and gynecology
Published: July 30, 2021

Genetic and Epigenetic Control of Puberty.

Genetic and Epigenetic Control of Puberty.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Published: August 15, 2020

Clinical and Molecular Cytogenetic Characteristics of Five Cases with Isodicentric Y Chromosome.

Clinical and Molecular Cytogenetic Characteristics of Five Cases with Isodicentric Y Chromosome.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Published: April 30, 2020

Identification of common differentially expressed genes in Turner (45,X) and Klinefelter (47,XXY) syndromes using bioinformatics analysis.

Identification of common differentially expressed genes in Turner (45,X) and Klinefelter (47,XXY) syndromes using bioinformatics analysis.

Journal: Molecular genetics & genomic medicine
Published: April 08, 2020

New findings in disorders of sex development: role of DMRT3 and OAS3.

New findings in disorders of sex development: role of DMRT3 and OAS3.

Journal: Fertility and sterility
Published: March 27, 2020

Disorders of sex development: Genetic characterization of a patient cohort.

Disorders of sex development: Genetic characterization of a patient cohort.

Journal: Molecular medicine reports
Published: March 28, 2019

Risk factors associated with congenital defects that alter hearing or vision in children born in the city of Bogotá between 2002 and 2016.

Risk factors associated with congenital defects that alter hearing or vision in children born in the city of Bogotá between 2002 and 2016.

Journal: International journal of pediatric otorhinolaryngology
Published: February 05, 2019
Showing 1-11 of 11

Last Updated: 09/26/2026