Layman LC - Search Results

1

Would combined glucocorticoid and gonadotropin therapy improve pregnancy rates in women with primary ovarian insufficiency?

Layman LC. Layman LC. F S Rep. 2020 Oct 22;1(3):171-172. doi: 10.1016/j.xfre.2020.10.003. eCollection 2020 Dec. F S Rep. 2020. PMID: 34223237 Free PMC article. No abstract available.

2

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

Theisen JG, Sundaram V, Filchak MS, Chorich LP, Sullivan ME, Knight J, Kim HG, Layman LC. Theisen JG, et al. Among authors: layman lc. Sci Rep. 2019 Dec 27;9(1):20099. doi: 10.1038/s41598-019-53500-y. Sci Rep. 2019. PMID: 31882810 Free PMC article.

3

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

Kim YJ, Osborn DP, Lee JY, Araki M, Araki K, Mohun T, Känsäkoski J, Brandstack N, Kim HT, Miralles F, Kim CH, Brown NA, Kim HG, Martinez-Barbera JP, Ataliotis P, Raivio T, Layman LC, Kim SH. Kim YJ, et al. Among authors: layman lc. EMBO Rep. 2018 Feb;19(2):269-289. doi: 10.15252/embr.201744632. Epub 2017 Dec 20. EMBO Rep. 2018. PMID: 29263200 Free PMC article.

4

Gonadotropin-releasing hormone-associated peptide gene sequences in women with hyperprolactinemia.

Moretuzzo RW, Layman LC, Tho SP, Reindollar RH, Gray MR, McDonough PG. Moretuzzo RW, et al. Among authors: layman lc. Fertil Steril. 1992 Nov;58(5):908-13. Fertil Steril. 1992. PMID: 1426375 Free article.

5

Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency.

Choi JH, Balasubramanian R, Lee PH, Shaw ND, Hall JE, Plummer L, Buck CL, Kottler ML, Jarzabek K, Wołczynski S, Quinton R, Latronico AC, Dode C, Ogata T, Kim HG, Layman LC, Gusella JF, Crowley WF Jr. Choi JH, et al. Among authors: layman lc. J Clin Endocrinol Metab. 2015 Oct;100(10):E1378-85. doi: 10.1210/jc.2015-2262. Epub 2015 Jul 24. J Clin Endocrinol Metab. 2015. PMID: 26207952 Free PMC article.

6

The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism.

Bhagavath B, Ozata M, Ozdemir IC, Bolu E, Bick DP, Sherins RJ, Layman LC. Bhagavath B, et al. Among authors: layman lc. Fertil Steril. 2005 Oct;84(4):951-7. doi: 10.1016/j.fertnstert.2005.04.029. Fertil Steril. 2005. PMID: 16213849

7

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 LP, Tam KB, Lossie AC, Kim HG, Knight J, Taylor HS, Mukherjee S, Capra JA, Phillips JA 3rd, Friez M, Layman LC. Mikhael S, et al. Among authors: layman lc. Hum Genet. 2021 Apr;140(4):667-680. doi: 10.1007/s00439-020-02239-y. Epub 2021 Jan 19. Hum Genet. 2021. PMID: 33469725 Free PMC article.

8

Genetics of hypogonadotropic Hypogonadism-Human and mouse genes, inheritance, oligogenicity, and genetic counseling.

Louden ED, Poch A, Kim HG, Ben-Mahmoud A, Kim SH, Layman LC. Louden ED, et al. Among authors: layman lc. Mol Cell Endocrinol. 2021 Aug 20;534:111334. doi: 10.1016/j.mce.2021.111334. Epub 2021 May 30. Mol Cell Endocrinol. 2021. PMID: 34062169 Review.

9

Analysis of the PROP1 gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadism.

Park JK, Ozata M, Chorich LP, Cheng L, Bick DP, Sherins RJ, Ozdemir IC, Bolu E, Cogan JD, Phillips JA, Layman LC. Park JK, et al. Among authors: layman lc. Clin Endocrinol (Oxf). 2004 Jan;60(1):147-9. doi: 10.1111/j.1365-2265.2004.01928.x. Clin Endocrinol (Oxf). 2004. PMID: 14678304 No abstract available.

10

Screening candidate genes for mutations in patients with hypogonadotropic hypogonadism using custom genome resequencing microarrays.

Xu N, Podolsky RH, Chudgar P, Chorich LP, Liu C, McDonough PG, Warrington JA, Layman LC. Xu N, et al. Among authors: layman lc. Am J Obstet Gynecol. 2005 Apr;192(4):1274-82; discussion 1282-4. doi: 10.1016/j.ajog.2004.12.066. Am J Obstet Gynecol. 2005. PMID: 15846219

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