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Results: 1 to 20 of 133

1.

Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease.

Okou DT, Mondal K, Faubion WA, Kobrynski LJ, Denson LA, Mulle JG, Ramachandran D, Xiong Y, Svingen P, Patel V, Bose P, Waters JP, Prahalad S, Cutler DJ, Zwick ME, Kugathasan S.

J Pediatr Gastroenterol Nutr. 2014 May;58(5):561-8. doi: 10.1097/MPG.0000000000000302.

PMID:
24792626
[PubMed - in process]
2.

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.

Mulle JG, Pulver AE, McGrath JA, Wolyniec PS, Dodd AF, Cutler DJ, Sebat J, Malhotra D, Nestadt G, Conrad DF, Hurles M, Barnes CP, Ikeda M, Iwata N, Levinson DF, Gejman PV, Sanders AR, Duan J, Mitchell AA, Peter I, Sklar P, O'Dushlaine CT, Grozeva D, O'Donovan MC, Owen MJ, Hultman CM, Kähler AK, Sullivan PF; Molecular Genetics of Schizophrenia Consortium, Kirov G, Warren ST.

Biol Psychiatry. 2014 Mar 1;75(5):371-7. doi: 10.1016/j.biopsych.2013.05.040. Epub 2013 Jul 17.

PMID:
23871472
[PubMed - in process]
3.

A comprehensive search for recombinogenic motifs in the human genome.

Johnston HR, Cutler DJ.

PLoS One. 2013 Apr 23;8(4):e62920. doi: 10.1371/journal.pone.0062920. Print 2013.

PMID:
23626862
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Susceptibility to childhood-onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci.

Prahalad S, Conneely KN, Jiang Y, Sudman M, Wallace CA, Brown MR, Ponder LA, Rohani-Pichavant M, Zwick ME, Cutler DJ, Angeles-Han ST, Vogler LB, Kennedy C, Rouster-Stevens K, Wise CA, Punaro M, Reed AM, Mellins ED, Bohnsack JF, Glass DN, Thompson SD.

Arthritis Rheum. 2013 Jun;65(6):1663-7. doi: 10.1002/art.37913.

PMID:
23450725
[PubMed - indexed for MEDLINE]
Free PMC Article
5.
6.

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder.

Steinberg KM, Ramachandran D, Patel VC, Shetty AC, Cutler DJ, Zwick ME.

Mol Autism. 2012 Sep 28;3(1):8. doi: 10.1186/2040-2392-3-8.

PMID:
23020841
[PubMed]
Free PMC Article
7.

Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder.

Mondal K, Ramachandran D, Patel VC, Hagen KR, Bose P, Cutler DJ, Zwick ME.

Hum Mol Genet. 2012 Oct 1;21(19):4356-64. doi: 10.1093/hmg/dds267. Epub 2012 Jul 5.

PMID:
22773736
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Population demographic history can cause the appearance of recombination hotspots.

Johnston HR, Cutler DJ.

Am J Hum Genet. 2012 May 4;90(5):774-83. doi: 10.1016/j.ajhg.2012.03.011.

PMID:
22560089
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Genistein cooperates with the histone deacetylase inhibitor vorinostat to induce cell death in prostate cancer cells.

Phillip CJ, Giardina CK, Bilir B, Cutler DJ, Lai YH, Kucuk O, Moreno CS.

BMC Cancer. 2012 Apr 11;12:145. doi: 10.1186/1471-2407-12-145.

PMID:
22494660
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture.

Adeyanju O, Okou DT, Huang C, Kumar A, Sauer C, Galloway C, Prasad M, Waters J, Cutler DJ, Zwick ME, Dhere T, Kugathasan S.

Inflamm Bowel Dis. 2012 Dec;18(12):2357-9. doi: 10.1002/ibd.22944. Epub 2012 Mar 22.

PMID:
22447396
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.

Sun M, Mondal K, Patel V, Horner VL, Long AB, Cutler DJ, Caspary T, Zwick ME.

G3 (Bethesda). 2012 Jan;2(1):143-50. doi: 10.1534/g3.111.001669. Epub 2012 Jan 1.

PMID:
22384391
[PubMed]
Free PMC Article
12.

Association study of serotonin pathway genes in attempted suicide.

Judy JT, Seifuddin F, Mahon PB, Huo Y, Goes FS, Jancic D, Schweizer B, Mondimore FM, Mackinnon DF, Depaulo JR Jr, Gershon ES, McMahon FJ, Cutler DJ, Zandi PP, Potash JB, Willour VL.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):112-9. doi: 10.1002/ajmg.b.32008. Epub 2011 Dec 13.

PMID:
22170779
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry.

Wingo TS, Cutler DJ, Yarab N, Kelly CM, Glass JD.

PLoS One. 2011;6(11):e27985. doi: 10.1371/journal.pone.0027985. Epub 2011 Nov 22.

PMID:
22132186
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Autosomal recessive causes likely in early-onset Alzheimer disease.

Wingo TS, Lah JJ, Levey AI, Cutler DJ.

Arch Neurol. 2012 Jan;69(1):59-64. doi: 10.1001/archneurol.2011.221. Epub 2011 Sep 12.

PMID:
21911656
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Targeted sequencing of the human X chromosome exome.

Mondal K, Shetty AC, Patel V, Cutler DJ, Zwick ME.

Genomics. 2011 Oct;98(4):260-5. doi: 10.1016/j.ygeno.2011.04.004. Epub 2011 Apr 16.

PMID:
21524701
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Microarray oligonucleotide probe designer (MOPeD): A web service.

Patel VC, Mondal K, Shetty AC, Horner VL, Bedoyan JK, Martin D, Caspary T, Cutler DJ, Zwick ME.

Open Access Bioinformatics. 2010 Nov 1;2(2010):145-155.

PMID:
21379402
[PubMed]
Free PMC Article
17.

Paraoxonase-1 polymorphisms in Alzheimer's disease, Parkinson's disease, and AD-PD spectrum diseases.

Wingo TS, Rosen A, Cutler DJ, Lah JJ, Levey AI.

Neurobiol Aging. 2012 Jan;33(1):204.e13-5. doi: 10.1016/j.neurobiolaging.2010.08.010. Epub 2010 Oct 13.

PMID:
20947215
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

To pool, or not to pool?

Cutler DJ, Jensen JD.

Genetics. 2010 Sep;186(1):41-3. doi: 10.1534/genetics.110.121012. No abstract available.

PMID:
20855575
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

SeqAnt: a web service to rapidly identify and annotate DNA sequence variations.

Shetty AC, Athri P, Mondal K, Horner VL, Steinberg KM, Patel V, Caspary T, Cutler DJ, Zwick ME.

BMC Bioinformatics. 2010 Sep 20;11:471. doi: 10.1186/1471-2105-11-471.

PMID:
20854673
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.

Collins SC, Bray SM, Suhl JA, Cutler DJ, Coffee B, Zwick ME, Warren ST.

Am J Med Genet A. 2010 Oct;152A(10):2512-20. doi: 10.1002/ajmg.a.33626.

PMID:
20799337
[PubMed - indexed for MEDLINE]
Free PMC Article

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