HD033004/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2008	2
2009	2
2010	3
2011	3
2012	2
2013	6
2014	2
2015	3
2016	1
2017	2
2018	2
2020	1
2024	0

1

Clinical genetic testing for Kallmann syndrome.

Layman LC. Layman LC. J Clin Endocrinol Metab. 2013 May;98(5):1860-2. doi: 10.1210/jc.2013-1624. J Clin Endocrinol Metab. 2013. PMID: 23650337 Free PMC article. No abstract available.

2

Genotype and phenotype of patients with gonadotropin-releasing hormone receptor mutations.

Kim HG, Pedersen-White J, Bhagavath B, Layman LC. Kim HG, et al. Front Horm Res. 2010;39:94-110. doi: 10.1159/000312696. Epub 2010 Apr 8. Front Horm Res. 2010. PMID: 20389088 Free PMC article. Review.

3

The genetic basis of female reproductive disorders: etiology and clinical testing.

Layman LC. Layman LC. Mol Cell Endocrinol. 2013 May 6;370(1-2):138-48. doi: 10.1016/j.mce.2013.02.016. Epub 2013 Mar 14. Mol Cell Endocrinol. 2013. PMID: 23499866 Free PMC article. Review.

4

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

Williams LS, Demir Eksi D, Shen Y, Lossie AC, Chorich LP, Sullivan ME, Phillips JA 3rd, Erman M, Kim HG, Alper OM, Layman LC. Williams LS, et al. Fertil Steril. 2017 Jul;108(1):145-151.e2. doi: 10.1016/j.fertnstert.2017.05.017. Epub 2017 Jun 7. Fertil Steril. 2017. PMID: 28600106 Free PMC article.

5

The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models.

Siegel ET, Kim HG, Nishimoto HK, Layman LC. Siegel ET, et al. Reprod Sci. 2013 Mar;20(3):211-33. doi: 10.1177/1933719112461184. Epub 2012 Nov 26. Reprod Sci. 2013. PMID: 23184658 Free PMC article. Review.

6

The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Kim HG, Layman LC. Kim HG, et al. Mol Cell Endocrinol. 2011 Oct 22;346(1-2):74-83. doi: 10.1016/j.mce.2011.07.013. Epub 2011 Aug 2. Mol Cell Endocrinol. 2011. PMID: 21856375 Free PMC article. Review.

7

Genetic considerations in the patient with Turner syndrome--45,X with or without mosaicism.

Zhong Q, Layman LC. Zhong Q, et al. Fertil Steril. 2012 Oct;98(4):775-9. doi: 10.1016/j.fertnstert.2012.08.021. Fertil Steril. 2012. PMID: 23020909 Free PMC article. Review.

8

Identification of HESX1 mutations in Kallmann syndrome.

Newbern K, Natrajan N, Kim HG, Chorich LP, Halvorson LM, Cameron RS, Layman LC. Newbern K, et al. Fertil Steril. 2013 Jun;99(7):1831-7. doi: 10.1016/j.fertnstert.2013.01.149. Epub 2013 Mar 1. Fertil Steril. 2013. PMID: 23465708 Free PMC article.

9

Long-term follow-up of females with unbalanced X;Y translocations-reproductive and nonreproductive consequences.

Dobek WA, Kim HG, Walls CA, Chorich LP, Tho SP, Wang ZX, McDonough PG, Layman LC. Dobek WA, et al. Mol Cytogenet. 2015 Feb 22;8:13. doi: 10.1186/s13039-015-0112-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 25737742 Free PMC article.

10

Long-Term Follow-Up and Treatment of a Female With Complete Estrogen Insensitivity.

Brakta S, Chorich LP, Kim HG, Coons LA, Katzenellenbogen JA, Hall JE, Korach KS, Layman LC. Brakta S, et al. J Clin Endocrinol Metab. 2020 May 1;105(5):1478-88. doi: 10.1210/clinem/dgaa106. J Clin Endocrinol Metab. 2020. PMID: 32152632 Free PMC article.

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