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Lawrence C Layman

Section Chief

  • 3300 Citations
  • 33 h-Index
1985 …2019

Research output per year

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Projects

Genetics of Mullerian Development

Layman, L. C.

National Institutes of Health

Project: Research project

    • Genotype /phenotype correlations in infertility

    Layman, L. C.

    National Institutes of Health

    8/14/02 → 7/31/08

    Project: Research project

    • GENETICS OF DELAYED PUBERTY

    Layman, L. C.

    National Institutes of Health

    7/1/97 → 3/31/16

    Project: Research project

    • Research Output

    Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism

    Kim, H. G., Rosenfeld, J. A., Scott, D. A., Bénédicte, G., Labonne, J. D., Brown, J., McGuire, M., Mahida, S., Naidu, S., Gutierrez, J., Lesca, G., Des Portes, V., Bruel, A. L., Sorlin, A., Xia, F., Capri, Y., Muller, E., McKnight, D., Torti, E., Rüschendorf, F. & 8 others, Hummel, O., Islam, Z., Kolatkar, P. R., Layman, L. C., Ryu, D., Kong, I. K., Madan-Khetarpal, S. & Kim, C. H., Oct 22 2019, In : Molecular Autism. 10, 1, 35.

    Research output: Contribution to journal › Article

    Open Access

    • The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants

    Theisen, J. G., Sundaram, V., Filchak, M. S., Chorich, L. P., Sullivan, M. E., Knight, J., Kim, H. G. & Layman, L. C., Dec 1 2019, In : Scientific Reports. 9, 1, 20099.

    Research output: Contribution to journal › Article

    Open Access

    • Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia

    Demir Eksi, D., Shen, Y., Erman, M., Chorich, L. P., Sullivan, M. E., Bilekdemir, M., Yllmaz, E., Luleci, G., Kim, H. G., Alper, O. M. & Layman, L. C., Feb 3 2018, In : Molecular Cytogenetics. 11, 1, 13.

    Research output: Contribution to journal › Article

    • 2 Scopus citations

    JAK/STAT signaling pathway gene expression is reduced following Nelf knockdown in GnRH neurons

    Ko, E. K., Chorich, L. P., Sullivan, M. E., Cameron, R. S. & Layman, L. C., Jul 15 2018, In : Molecular and Cellular Endocrinology. 470, p. 151-159 9 p.

    Research output: Contribution to journal › Article

    • 2 Scopus citations

    WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

    Kim, Y. J., Osborn, D. P. S., Lee, J. Y., Araki, M., Araki, K., Mohun, T., Känsäkoski, J., Brandstack, N., Kim, H. T., Miralles, F., Kim, C. H., Brown, N. A., Kim, H. G., Martinez-Barbera, J. P., Ataliotis, P., Raivio, T., Layman, L. C. & Kim, S. H., Feb 1 2018, In : EMBO Reports. 19, 2, p. 269-289 21 p.

    Research output: Contribution to journal › Article

    • 4 Scopus citations