Lawrence C. Layman

Obstetrics and Gynecology

810 Chafee Ave
Augusta, GA 30904

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 78 publications

Sex differences in cardiovascular disease risk in type 1 diabetes: The vascular bed paradox in women.

Sex differences in cardiovascular disease risk in type 1 diabetes: The vascular bed paradox in women.

Journal: Diabetes & vascular disease research

Published: May 30, 2026

Genetics in Reproduction.

Genetics in Reproduction.

Journal: Seminars in reproductive medicine

Published: April 08, 2026

Clinical Genetics in Reproductive Medicine: Variant Classification, Medically Actionable Genes, and Carrier Screening.

Clinical Genetics in Reproductive Medicine: Variant Classification, Medically Actionable Genes, and Carrier Screening.

Journal: Seminars in reproductive medicine

Published: March 17, 2026

Clinical Testing for Genetic Conditions.

Clinical Testing for Genetic Conditions.

Journal: Seminars in reproductive medicine

Published: March 11, 2026

Overestimation of Pathogenic Variants in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome.

Overestimation of Pathogenic Variants in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome.

Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists

Published: December 17, 2025

Overestimation of Pathogenic Variants in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome.

Overestimation of Pathogenic Variants in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome.

Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists

Published: December 17, 2025

The prevalence of pathogenic variants in medically actionable genes among individuals with idiopathic hypogonadotropic hypogonadism/Kallmann syndrome.

The prevalence of pathogenic variants in medically actionable genes among individuals with idiopathic hypogonadotropic hypogonadism/Kallmann syndrome.

Journal: Journal of assisted reproduction and genetics

Published: September 12, 2025

Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.

Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.

Journal: Human genetics

Published: April 15, 2025

Transgender identity genetic research: Attitudes, opinions & beliefs among members of the transgender and gender diverse communities.

Transgender identity genetic research: Attitudes, opinions & beliefs among members of the transgender and gender diverse communities.

Journal: International journal of transgender health

Published: October 28, 2024

Ovotesticular Disorders of sexual development (DSD): A rare case of peritoneal carcinomatosis in an elderly DSD male patient.

Ovotesticular Disorders of sexual development (DSD): A rare case of peritoneal carcinomatosis in an elderly DSD male patient.

Journal: Gynecologic oncology reports

Published: June 24, 2024

Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG).

Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG).

Journal: American journal of medical genetics. Part A

Published: June 02, 2024

Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women.

Identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women.

Journal: F&S science

Published: April 01, 2024

Showing 1-12 of 78

Last Updated: 09/26/2026