• 3452 Citations
  • 34 h-Index
1985 …2020

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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Genotype /phenotype correlations in infertility

Layman, L. C.


Project: Research project


Layman, L. C.


Project: Research project

Research Output

Academic pursuits in board-certified reproductive endocrinologists

Layman, L. C., Feinberg, E. C., Hurst, B. S., Morin, S. J., Morris, J. L., Pisarska, M. D., Smith, Y. R. & Price, T. M., Mar 2020, In : Fertility and sterility. 113, 3, p. 653-660.e1

Research output: Contribution to journalArticle

  • 1 Scopus citations

    Long-term follow-up and treatment of a female with complete estrogen insensitivity

    Brakta, S., Chorich, L. P., Kimt, H. G., Coons, L. A., Katzenellenbogen, J. A., Hall, J. E., Korach, K. S. & Layman, L. C., May 1 2020, In : Journal of Clinical Endocrinology and Metabolism. 105, 5, dgaa106.

    Research output: Contribution to journalArticle

  • 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

  • 3 Scopus citations