• 3300 Citations
  • 33 h-Index
1985 …2019

Research output per year

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Fingerprint Dive into the research topics where Lawrence C Layman is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Projects

  • 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 journalArticle

    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 journalArticle

    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 journalArticle

  • 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 journalArticle

  • 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 journalArticle

  • 4 Scopus citations