Lawrence C Layman
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Explore the profile of Lawrence C Layman including associated specialties, affiliations and a list of published articles.
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96
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1649
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Recent Articles
1.
Ghasemi M, Tehrani Fateh S, Ben-Mahmoud A, Gupta V, Stuhn L, Lesca G, et al.
Am J Med Genet A
. 2024 Dec;
:e63963.
PMID: 39707601
The Houge type of X-linked syndromic intellectual developmental disorder (MRXSHG) encompasses a spectrum of neurodevelopmental disorders characterized by intellectual disability (ID), language/speech delay, attention issues, and epilepsy. These conditions arise...
2.
Theisen J, Draheim A, Darosh A, Layman L, Stepleman L
Int J Transgend Health
. 2024 Oct;
25(4):971-984.
PMID: 39465081
There is growing interest in investigating genetic explanations for transgender identity. In the spirit of a Community-Engaged Research Framework, which highlights the importance of involving community members who would be...
3.
Navitski A, Sehgal S, Ballur K, Layman L, Higgins R
Gynecol Oncol Rep
. 2024 Oct;
56:101515.
PMID: 39391706
Disorders of sexual development (DSDs) represent a spectrum of conditions characterized by atypical gonadal and/or genital development. The incidence is 1 in 5,000 live births. Patients with DSD may be...
4.
Ghasemi M, Sadeghi H, Hashemi-Gorji F, Mirfakhraie R, Gupta V, Ben-Mahmoud A, et al.
BMC Med Genomics
. 2024 Aug;
17(1):196.
PMID: 39103847
Background And Objective: Autosomal recessive genetic disorders pose significant health challenges in regions where consanguineous marriages are prevalent. The utilization of exome sequencing as a frequently employed methodology has enabled...
5.
Theisen J, Chorich L, Xu H, Knight J, Kim H, Layman L
F S Sci
. 2024 Jun;
5(3):283-292.
PMID: 38942387
Objective: To study the identification of rare genetic variants in the PCDH genetic family in a cohort of transgender women (TGW) and their potential role in gender identity. Design: Exome...
6.
Brakta S, Du Q, Chorich L, Hawkins Z, Sullivan M, Ko E, et al.
Mol Cell Endocrinol
. 2024 Apr;
589:112237.
PMID: 38599276
The molecular basis of mullerian aplasia, also known as Mayer-Rokitansky-Kuster Hauser (MRKH) or congenital absence of the uterus and vagina, is largely unknown. We applied a multifaceted genetic approach to...
7.
Poch A, Dougherty M, Roman R, Chorich L, Hawkins Z, Kim S, et al.
Mol Cell Endocrinol
. 2024 Apr;
589:112224.
PMID: 38593951
Background: Hypogonadotropic hypogonadism (HH) is due to impaired gonadotropin releasing hormone (GnRH) action resulting in absent puberty and infertility. At least 44 genes have been identified to possess genetic variants...
8.
Gupta V, Ben-Mahmoud A, Ku B, Velayutham D, Jan Z, Yousef Aden A, et al.
Front Psychiatry
. 2023 Nov;
14:1251884.
PMID: 38025430
This study investigated the genetic underpinnings of autism spectrum disorder (ASD) in a Middle Eastern cohort in Qatar using exome sequencing. The study identified six candidate autism genes in independent...
9.
Simon A, Derella C, Blackburn M, Thomas J, Layman L, Nicholson M, et al.
Cardiovasc Diabetol
. 2023 Sep;
22(1):243.
PMID: 37679748
Background: Endogenous estrogen is cardio-protective in healthy premenopausal women. Despite this favorable action of estrogen, animal models depict a detrimental effect of estradiol on vascular function in the presence of...
10.
Ben-Mahmoud A, Kishikawa S, Gupta V, Leach N, Shen Y, Moldovan O, et al.
Sci Rep
. 2023 Aug;
13(1):12984.
PMID: 37563198
In a patient diagnosed with both Kallmann syndrome (KS) and intellectual disability (ID), who carried an apparently balanced translocation t(7;12)(q22;q24)dn, array comparative genomic hybridization (aCGH) disclosed a cryptic heterozygous 4.7...