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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.

  • 7 Similar Profiles
Hypogonadism Medicine & Life Sciences
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Kallmann Syndrome Medicine & Life Sciences
Gonadotropin-Releasing Hormone Medicine & Life Sciences
Follicle Stimulating Hormone Medicine & Life Sciences
LHRH Receptors Medicine & Life Sciences
Primary Ovarian Insufficiency Medicine & Life Sciences

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Projects 1997 2016

Genetic Association Studies
Infertility
Puberty
Mutation
Beta Subunit Follicle Stimulating Hormone
Delayed Puberty
Gonadotropin-Releasing Hormone
Mutation
Genes
Kallmann Syndrome

Research Output 1985 2018

1 Citation (Scopus)

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

Genes
Microarrays
Chromosomes
Animals
Western World
1 Citation (Scopus)

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

Janus Kinases
Transcription
Transducers
Gene expression
Gonadotropin-Releasing Hormone
3 Citations (Scopus)

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

Kallmann Syndrome
Hedgehogs
Hypogonadism
Defects
Gene expression
5 Citations (Scopus)

Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families

Williams, L. S., Demir Eksi, D., Shen, Y., Lossie, A. C., Chorich, L. P., Sullivan, M. E., Phillips, J. A., Erman, M., Kim, H. G., Alper, O. M. & Layman, L. C., Jul 1 2017, In : Fertility and sterility. 108, 1, p. 145-151.e2

Research output: Contribution to journalArticle

Point Mutation
Mullerian aplasia
Genetic Association Studies
Pedigree
Microarray Analysis
1 Citation (Scopus)

Genetic basis of eugonadal and hypogonadal female reproductive disorders

Trofimova, T., Lizneva, D., Suturina, L., Walker, W., Chen, Y-H., Azziz, R. & Layman, L. C., Oct 1 2017, In : Best Practice and Research: Clinical Obstetrics and Gynaecology. 44, p. 3-14 12 p.

Research output: Contribution to journalReview article

Hypogonadism
Kallmann Syndrome
Ovarian Hyperstimulation Syndrome
Primary Ovarian Insufficiency
Turner Syndrome