Mehdi Keddache

Mehdi Keddache

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Mehdi Keddache

Mehdi Keddache

Publications by authors named "Mehdi Keddache"

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34Publications

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Dissecting the Genetic Susceptibility to Graves' Disease in a Cohort of Patients of Italian Origin.

Front Endocrinol (Lausanne) 2016 8;7:21. Epub 2016 Mar 8.

Division of Endocrinology, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Bronx VA Medical Center, Bronx, NY, USA.

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http://dx.doi.org/10.3389/fendo.2016.00021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4781855PMC
March 2016

MicroRNA activation signature in patients with hemophagocytic lymphohistiocytosis and reversibility with disease-specific therapy.

J Allergy Clin Immunol 2016 Jan 17;137(1):309-312. Epub 2015 Jul 17.

Division of Bone Marrow Transplantation and Immune Deficiency, Blood and Cancer Research Institute, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Faculty of Medicine, Cincinnati, Ohio.

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http://dx.doi.org/10.1016/j.jaci.2015.06.006DOI Listing
January 2016

Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse model.

Hum Mol Genet 2015 Dec 29;24(24):7031-48. Epub 2015 Sep 29.

Division of Human Genetics, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229, USA, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA

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http://dx.doi.org/10.1093/hmg/ddv404DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4654057PMC
December 2015

Whole exome sequencing for familial bicuspid aortic valve identifies putative variants.

Circ Cardiovasc Genet 2014 Oct 1;7(5):677-83. Epub 2014 Aug 1.

From the Department of Pediatrics, Cincinnati Children's Hospital Medical Center, OH (L.J.M., V.P., K.M.K., L.C.K., M.K., P.D., M.T.W.); Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati OH (L.J.M., K.M.K., M.K., M.T.W.); Department of Pediatrics, Nationwide Children's Hospital, The Ohio State University, Columbus (L.C.); Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee (D.W.B.); and Department of Pediatrics, Medical College of Wisconsin, Milwaukee (D.W.B.).

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http://dx.doi.org/10.1161/CIRCGENETICS.114.000526DOI Listing
October 2014

EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children.

Front Genet 2013 3;4:268. Epub 2013 Dec 3.

Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center Cincinnati, OH, USA ; Cincinnati Children's Hospital Medical Center Cincinnati, OH, USA ; School of Medicine, University of Cincinnati Cincinnati, OH, USA ; Department of Veteran Affairs Medical Center Cincinnati, OH, USA.

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http://journal.frontiersin.org/article/10.3389/fgene.2013.00
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http://dx.doi.org/10.3389/fgene.2013.00268DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847941PMC
December 2013

Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.

Otolaryngol Head Neck Surg 2013 Jun 22;148(6):1007-16. Epub 2013 Mar 22.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.

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http://dx.doi.org/10.1177/0194599813482294DOI Listing
June 2013

From single-SNP to wide-locus: genome-wide association studies identifying functionally related genes and intragenic regions in small sample studies.

Pharmacogenomics 2013 Mar;14(4):391-401

Center for Clinical & Translational Science, The Rockefeller University, 1230 York Ave Box 322, New York, NY 10021, USA.

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http://dx.doi.org/10.2217/pgs.13.28DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643309PMC
March 2013

Fine mapping of loci linked to autoimmune thyroid disease identifies novel susceptibility genes.

J Clin Endocrinol Metab 2013 Jan 1;98(1):E144-52. Epub 2012 Nov 1.

Department of Medicine, Division of Endocrinology, Mount Sinai School of Medicine, New York, New York 10029, USA.

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http://dx.doi.org/10.1210/jc.2012-2408DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537111PMC
January 2013

Novel variations in the adiponectin gene (ADIPOQ) may affect distribution of oligomeric complexes.

Springerplus 2012 Dec 14;1(1):66. Epub 2012 Dec 14.

Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 4006, Cincinnati, OH 45229 USA.

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http://dx.doi.org/10.1186/2193-1801-1-66DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565092PMC
December 2012

IFN-α mediates the development of autoimmunity both by direct tissue toxicity and through immune cell recruitment mechanisms.

J Immunol 2011 Apr 14;186(8):4693-706. Epub 2011 Mar 14.

Division of Endocrinology, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.

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http://dx.doi.org/10.4049/jimmunol.1002631DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3106338PMC
April 2011

Analysis of immune regulatory genes' copy number variants in Graves' disease.

Thyroid 2011 Jan 8;21(1):69-74. Epub 2010 Nov 8.

Division of Endocrinology, Department of Medicine, Mount Sinai School of Medicine, New York, New York 10029, USA.

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http://dx.doi.org/10.1089/thy.2010.0262DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012451PMC
January 2011

Polymorphisms in the IBD5 locus are associated with Crohn disease in pediatric Ashkenazi Jewish patients.

J Pediatr Gastroenterol Nutr 2009 May;48(5):531-7

Department of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, MLC 2010, Cincinnati, OH 45229, USA.

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https://insights.ovid.com/crossref?an=00005176-200905000-000
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http://dx.doi.org/10.1097/MPG.0b013e318183138aDOI Listing
May 2009

A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.

Mov Disord 2009 Feb;24(3):364-70

Division of Neurology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, Ohio 45229-3039, USA.

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http://dx.doi.org/10.1002/mds.22363DOI Listing
February 2009

Multiple interactions between the alpha 2C- and beta1-adrenergic receptors influence heart failure survival.

BMC Med Genet 2008 Oct 23;9:93. Epub 2008 Oct 23.

Department of Epidemiology, School of Public Health, University of Michigan, 109 Observatory St,, Ann Arbor, MI 48109-2029, USA.

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http://dx.doi.org/10.1186/1471-2350-9-93DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2588439PMC
October 2008

Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy.

Neurosci Lett 2008 Mar 11;433(1):65-70. Epub 2008 Jan 11.

Division of Neurology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S030439400701323
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http://dx.doi.org/10.1016/j.neulet.2007.12.064DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423278PMC
March 2008

Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations.

Hum Genet 2007 Apr 4;121(2):275-84. Epub 2007 Jan 4.

Center for Epidemiology and Biostatistics, University of Cincinnati, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

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http://link.springer.com/10.1007/s00439-006-0316-9
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http://dx.doi.org/10.1007/s00439-006-0316-9DOI Listing
April 2007

Characterization of neuronopathic Gaucher disease among ethnic Poles.

Genet Med 2006 Jan;8(1):8-15

Department of Metabolic Diseases, The Children's Memorial Health Institute, Warsaw, Poland.

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http://dx.doi.org/10.109701.gim.0000196443.42899.25DOI Listing
January 2006

Efficient PCR-based gene disruption in Saccharomyces strains using intergenic primers.

Yeast 2002 Mar;19(4):319-28

Department of Genetics and Development, Columbia University College of Physicians and Surgeons, New York, NY 10032-2704, USA.

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http://dx.doi.org/10.1002/yea.817DOI Listing
March 2002