Gharani N - Search Results

1

Cognitive traits link to human chromosomal regions.

Buyske S, Bates ME, Gharani N, Matise TC, Tischfield JA, Manowitz P. Buyske S, et al. Among authors: gharani n. Behav Genet. 2006 Jan;36(1):65-76. doi: 10.1007/s10519-005-9008-9. Epub 2005 Dec 10. Behav Genet. 2006. PMID: 16341908

2

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.

Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA, Dicicco-Bloom E, Brzustowicz LM, Millonig JH. Benayed R, et al. Among authors: gharani n. Am J Hum Genet. 2005 Nov;77(5):851-68. doi: 10.1086/497705. Epub 2005 Oct 5. Am J Hum Genet. 2005. PMID: 16252243 Free PMC article.

3

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.

Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH. Gharani N, et al. Mol Psychiatry. 2004 May;9(5):474-84. doi: 10.1038/sj.mp.4001498. Mol Psychiatry. 2004. PMID: 15024396

4

Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.

Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM, Millonig JH. Benayed R, et al. Among authors: gharani n. Biol Psychiatry. 2009 Nov 15;66(10):911-7. doi: 10.1016/j.biopsych.2009.05.027. Epub 2009 Jul 17. Biol Psychiatry. 2009. PMID: 19615670 Free PMC article.

5

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.

Bartlett CW, Gharani N, Millonig JH, Brzustowicz LM. Bartlett CW, et al. Among authors: gharani n. Int J Dev Neurosci. 2005 Apr-May;23(2-3):221-34. doi: 10.1016/j.ijdevneu.2004.10.004. Int J Dev Neurosci. 2005. PMID: 15749247 Review.

6

Variation in genome-wide mutation rates within and between human families.

Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, Hurles ME, Awadalla P; 1000 Genomes Project. Conrad DF, et al. Nat Genet. 2011 Jun 12;43(7):712-4. doi: 10.1038/ng.862. Nat Genet. 2011. PMID: 21666693 Free PMC article.

7

Genetic risk estimation in the Coriell Personalized Medicine Collaborative.

Stack CB, Gharani N, Gordon ES, Schmidlen T, Christman MF, Keller MA. Stack CB, et al. Among authors: gharani n. Genet Med. 2011 Feb;13(2):131-9. doi: 10.1097/GIM.0b013e318201164c. Genet Med. 2011. PMID: 21233721 Free article.

8

Association of the steroid synthesis gene CYP11a with polycystic ovary syndrome and hyperandrogenism.

Gharani N, Waterworth DM, Batty S, White D, Gilling-Smith C, Conway GS, McCarthy M, Franks S, Williamson R. Gharani N, et al. Hum Mol Genet. 1997 Mar;6(3):397-402. doi: 10.1093/hmg/6.3.397. Hum Mol Genet. 1997. PMID: 9147642

9

Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome.

Waterworth DM, Bennett ST, Gharani N, McCarthy MI, Hague S, Batty S, Conway GS, White D, Todd JA, Franks S, Williamson R. Waterworth DM, et al. Among authors: gharani n. Lancet. 1997 Apr 5;349(9057):986-90. doi: 10.1016/S0140-6736(96)08368-7. Lancet. 1997. PMID: 9100625

10

Integrative annotation of variants from 1092 humans: application to cancer genomics.

Khurana E, Fu Y, Colonna V, Mu XJ, Kang HM, Lappalainen T, Sboner A, Lochovsky L, Chen J, Harmanci A, Das J, Abyzov A, Balasubramanian S, Beal K, Chakravarty D, Challis D, Chen Y, Clarke D, Clarke L, Cunningham F, Evani US, Flicek P, Fragoza R, Garrison E, Gibbs R, Gümüş ZH, Herrero J, Kitabayashi N, Kong Y, Lage K, Liluashvili V, Lipkin SM, MacArthur DG, Marth G, Muzny D, Pers TH, Ritchie GRS, Rosenfeld JA, Sisu C, Wei X, Wilson M, Xue Y, Yu F; 1000 Genomes Project Consortium; Dermitzakis ET, Yu H, Rubin MA, Tyler-Smith C, Gerstein M. Khurana E, et al. Science. 2013 Oct 4;342(6154):1235587. doi: 10.1126/science.1235587. Science. 2013. PMID: 24092746 Free PMC article.

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