Lawrence C. Layman

Augusta University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

29h-index2.9kcitations99works0.92yr avg
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Research Topics

Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities(29), Sexual Differentiation and Disorders(28), Genetics and Neurodevelopmental Disorders(16), Reproductive Biology and Fertility(14), Hypothalamic control of reproductive hormones(14)

Publications99 total

THE PREVALENCE OF PATHOGENIC VARIANTS IN MEDICALLY ACTIONABLE GENES AMONG INDIVIDUALS WITH IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM/KALLMANN SYNDROME
Fertility and Sterility·2025
SUN-149 Low level Mosaic LHX1 Gene Deletion Contributes to Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome
Journal of the Endocrine Society·2025Open Access
Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of <scp><i>CNKSR2</i></scp> in the Houge Type of X‐Linked Syndromic Intellectual Development Disorder (<scp>MRXSHG</scp>)
American Journal of Medical Genetics Part A·2024Open Access
Ovotesticular Disorders of sexual development (DSD): A rare case of peritoneal carcinomatosis in an elderly DSD male patient
Gynecologic Oncology Reports·2024Open Access
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
BMC Medical Genomics·2024· 5 citedOpen Access
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)
Human Mutation·2024Open Access
Transgender identity genetic research: Attitudes, opinions &amp; beliefs among members of the transgender and gender diverse communities
International Journal of Transgender Health·2024· 2 citedOpen Access
Ovotesticular Disorders of Sexual Development (Dsd): A Rare Case of Peritoneal Carcinomatosis in an Elderly Dsd Male Patient
SSRN Electronic Journal·2024Open Access
Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing
Frontiers in Psychiatry·2023· 13 citedOpen Access
FRI410 ESR1 Variants Reduce Estrogen Receptor Alpha Expression In Women With Unexplained Infertility
Journal of the Endocrine Society·2023Open Access
R-SPONDIN 1 GENE VARIANT ASSOCIATED WITH 46,XX DIFFERENCE OF SEX DEVELOPMENT
Fertility and Sterility·2023Open Access
A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome
Scientific Reports·2023· 5 citedOpen Access
Coordination of canonical and noncanonical Hedgehog signalling pathways mediated by WDR11 during primordial germ cell development
Scientific Reports·2023· 6 citedOpen Access
Investigation of subfertility in the female Nsmf knockout mouse
F&S Science·2023Open Access
Digenic or oligogenic mutations in presumed monogenic disorders: A review
Journal of genetic medicine·2023· 5 citedOpen Access
A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome
Research Square (Research Square)·2023· 1 citedOpen Access
Identification of Rare Genetic Variants in the PCDH Genetic Family in a Cohort of Transgender Women
SSRN Electronic Journal·2023Open Access
OR06-3 ESR1 Pathogenic Variant With Incomplete Estrogen Insensitivity
Journal of the Endocrine Society·2022Open Access
A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders
Frontiers in Molecular Neuroscience·2022· 7 citedOpen Access
ESR1 HINGE REGION VARIANT IN A PATIENT WITH UNEXPLAINED INFERTILITY
Fertility and Sterility·2022
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Frequent Co-authors

Hyung‐Goo Kim(23), Paul G. McDonough(10), Jonathan D. J. Labonne(9), Lynn P. Chorich(6), Sandra P.T. Tho(6), Il‐Keun Kong(6), Yiping Shen(5), Cheol‐Hee Kim(5), Soo‐Hyun Kim(4), Julie R. Jones(4), Richard H. Reindollar(3), Jill A. Rosenfeld(3), Michael P. Diamond(3), David Bick(3), Leo Plouffe(3), Il‐Keun Kong(3), Franz Rüschendorf(3), Afif Ben‐Mahmoud(3), Kyungsoo Ha(3), Wolfgang Wenzel(3)