Projects per year
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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
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Genotype /phenotype correlations in infertility
Eunice Kennedy Shriver National Institute of Child Health and Human Development
8/14/02 → 7/31/08
Project: Research project
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Ethnic Differences in Stress Induced Sodium Regulation & Blood Pressure
Gutin, B., Layman, L., Pollock, D., Treiber, F., Pollock, J., Strong, W., Smith, D., George, V., Kapuku, K. G., Harshfield, G. A., Harshfield, G. A., Pollock, D., George, V., Dong, Y., Layman, L. C., George, V., Kapuku, K. G., George, V., Treiber, F., Gutin, B., Pollock, J., Strong, W., Smith, D., Layman, L., HARSHFIELD, G. A., Treiber, F., Pollock, J., Pollock, D., Dong, Y., Pollock, J., Pollock, D., Dong, Y., George, V., Pollock, J., Pollock, D., Dong, Y., George, V., Pollock, J., Pollock, D., George, V. & HARSHFIELD, G. A.
National Heart, Lung, and Blood Institute, National Institutes of Health
7/1/02 → 6/30/19
Project: Research project
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GENETICS OF DELAYED PUBERTY
Layman, L. C., Layman, L. C., Layman, L. C., Layman, L. C. & Layman, L. C.
Eunice Kennedy Shriver National Institute of Child Health and Human Development
7/1/97 → 3/31/16
Project: Research project
Research output
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Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer–Rokitansky–Küster–Hauser Syndrome
Mikhael, S., Dugar, S., Morton, M., Chorich, L. P., Tam, K. B., Lossie, A. C., Kim, H. G., Knight, J., Taylor, H. S., Mukherjee, S., Capra, J. A., Phillips, J. A., Friez, M. & Layman, L. C., 2021, (Accepted/In press) In: Human Genetics.Research output: Contribution to journal › Article › peer-review
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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.e1Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families
Doll, J., Vona, B., Schnapp, L., Rüschendorf, F., Khan, I., Khan, S., Muhammad, N., Khan, S. A., Nawaz, H., Khan, A., Ahmad, N., Kolb, S. M., Kühlewein, L., Labonne, J. D. J., Layman, L. C., Hofrichter, M. A. H., Röder, T., Dittrich, M., Müller, T., Graves, T. D. & 4 others, , Nov 2020, In: Genes. 11, 11, p. 1-16 16 p., 1329.Research output: Contribution to journal › Article › peer-review
Open Access -
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 journal › Article › peer-review
1 Scopus citations -
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, , Oct 22 2019, In: Molecular Autism. 10, 1, 35.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations