Lawrence C. Layman
Affiliations: | Molecular Medicine and Genetics | Georgia Regents University |
Area:
Genetics, Neuroscience Biology, Endocrinology Biology, Human DevelopmentGoogle:
"Lawrence Layman"Mean distance: 53433
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Publications
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| Ben-Mahmoud A, Kishikawa S, Gupta V, et al. (2023) 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. 13: 12984 |
| Ben-Mahmoud A, Kishikawa S, Gupta V, et al. (2023) 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 |
| Louden ED, Poch A, Kim HG, et al. (2021) Genetics of Hypogonadotropic Hypogonadism-Human and Mouse Genes, Inheritance, Oligogenicity, and Genetic Counseling. Molecular and Cellular Endocrinology. 111334 |
| Brakta S, Chorich LP, Kim HG, et al. (2020) Long-Term Follow Up and Treatment of a Female with Complete Estrogen Insensitivity. The Journal of Clinical Endocrinology and Metabolism |
| Labonne JDJ, Driessen TM, Harris ME, et al. (2020) Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp22.31. Journal of Clinical Medicine. 9 |
| Theisen JG, Sundaram V, Filchak MS, et al. (2019) The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants. Scientific Reports. 9: 20099 |
| Kim HG, Rosenfeld JA, Scott DA, et al. (2019) Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism. Molecular Autism. 10: 35 |
| Louden E, Ko EK, Chorich L, et al. (2019) SAT-404 Effect of Nsmf Knockout upon Hypothalamic and Pituitary Gene Expression in the Nsmf KO Mouse Journal of the Endocrine Society. 3 |
| Brakta S, Chorich L, Kim H, et al. (2019) OR15-4 Long-Term Follow-Up of a Female with a Mutation in the Estrogen Receptor Alpha (ESR1) Gene Journal of the Endocrine Society. 3 |
| Demir Eksi D, Shen Y, Erman M, et al. (2018) Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia. Molecular Cytogenetics. 11: 13 |