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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1980 2
1981 4
1982 2
1983 2
1984 5
1985 5
1986 12
1987 4
1988 10
1989 6
1990 10
1991 12
1992 8
1993 6
1994 10
1995 5
1996 13
1997 7
1998 9
1999 6
2000 3
2001 10
2002 5
2003 6
2004 5
2005 2
2006 5
2007 8
2008 11
2009 6
2010 7
2011 9
2012 3
2013 6
2014 3
2015 2
2016 1
2017 5
2021 1
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227 results
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Page 1
Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency.
Balasubramanian R, Crowley WF Jr. Balasubramanian R, et al. Among authors: crowley wf jr. 2007 May 23 [updated 2017 Mar 2]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. GeneReviews®. 1993–2021. PMID: 20301509 Free Books & Documents. Review.
The GPR54 gene as a regulator of puberty.
Seminara SB, Messager S, Chatzidaki EE, Thresher RR, Acierno JS Jr, Shagoury JK, Bo-Abbas Y, Kuohung W, Schwinof KM, Hendrick AG, Zahn D, Dixon J, Kaiser UB, Slaugenhaupt SA, Gusella JF, O'Rahilly S, Carlton MB, Crowley WF Jr, Aparicio SA, Colledge WH. Seminara SB, et al. Among authors: crowley wf jr. N Engl J Med. 2003 Oct 23;349(17):1614-27. doi: 10.1056/NEJMoa035322. N Engl J Med. 2003. PMID: 14573733 Free article.
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.
Miraoui H, Dwyer AA, Sykiotis GP, Plummer L, Chung W, Feng B, Beenken A, Clarke J, Pers TH, Dworzynski P, Keefe K, Niedziela M, Raivio T, Crowley WF Jr, Seminara SB, Quinton R, Hughes VA, Kumanov P, Young J, Yialamas MA, Hall JE, Van Vliet G, Chanoine JP, Rubenstein J, Mohammadi M, Tsai PS, Sidis Y, Lage K, Pitteloud N. Miraoui H, et al. Among authors: crowley wf jr. Am J Hum Genet. 2013 May 2;92(5):725-43. doi: 10.1016/j.ajhg.2013.04.008. Am J Hum Genet. 2013. PMID: 23643382 Free PMC article.
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.
Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME. Shaw ND, et al. Among authors: crowley wf jr. Nat Genet. 2017 Feb;49(2):238-248. doi: 10.1038/ng.3743. Epub 2017 Jan 9. Nat Genet. 2017. PMID: 28067909 Free PMC article.
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes.
Costa-Barbosa FA, Balasubramanian R, Keefe KW, Shaw ND, Al-Tassan N, Plummer L, Dwyer AA, Buck CL, Choi JH, Seminara SB, Quinton R, Monies D, Meyer B, Hall JE, Pitteloud N, Crowley WF Jr. Costa-Barbosa FA, et al. Among authors: crowley wf jr. J Clin Endocrinol Metab. 2013 May;98(5):E943-53. doi: 10.1210/jc.2012-4116. Epub 2013 Mar 26. J Clin Endocrinol Metab. 2013. PMID: 23533228 Free PMC article.
Hypogonadotropic hypogonadism.
Hayes FJ, Seminara SB, Crowley WF Jr. Hayes FJ, et al. Among authors: crowley wf jr. Endocrinol Metab Clin North Am. 1998 Dec;27(4):739-63, vii. doi: 10.1016/s0889-8529(05)70039-6. Endocrinol Metab Clin North Am. 1998. PMID: 9922906 Review.
Translational careers.
Andrews N, Burris JE, Cech TR, Coller BS, Crowley WF Jr, Gallin EK, Kelner KL, Kirch DG, Leshner AI, Morris CD, Nguyen FT, Oates J, Sung NS. Andrews N, et al. Among authors: crowley wf jr. Science. 2009 May 15;324(5929):855. doi: 10.1126/science.1172137. Science. 2009. PMID: 19443750 Free PMC article. No abstract available.
Reproductive endocrine phenotypes relating to CHD7 mutations in humans.
Balasubramanian R, Crowley WF Jr. Balasubramanian R, et al. Among authors: crowley wf jr. Am J Med Genet C Semin Med Genet. 2017 Dec;175(4):507-515. doi: 10.1002/ajmg.c.31585. Epub 2017 Nov 20. Am J Med Genet C Semin Med Genet. 2017. PMID: 29152903 Free PMC article. Review.
Male hypogonadotropic hypogonadism.
Whitcomb RW, Crowley WF Jr. Whitcomb RW, et al. Among authors: crowley wf jr. Endocrinol Metab Clin North Am. 1993 Mar;22(1):125-43. Endocrinol Metab Clin North Am. 1993. PMID: 8449184 Review.
Genetic counseling for isolated GnRH deficiency.
Au MG, Crowley WF Jr, Buck CL. Au MG, et al. Among authors: crowley wf jr. Mol Cell Endocrinol. 2011 Oct 22;346(1-2):102-9. doi: 10.1016/j.mce.2011.05.041. Epub 2011 Jun 1. Mol Cell Endocrinol. 2011. PMID: 21664415 Free PMC article. Review.
227 results
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