Marcella Devoto

Marcella Devoto

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Marcella Devoto

Publications by authors named "Marcella Devoto"

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A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1.

PLoS Genet 2018 08 13;14(8):e1007532. Epub 2018 Aug 13.

Division of Human Genetics, Department of Pediatrics, at The Children's Hospital of Philadelphia, and The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1007532DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107291PMC
August 2018

Novel ZBTB24 Mutation Associated with Immunodeficiency, Centromere Instability, and Facial Anomalies Type-2 Syndrome Identified in a Patient with Very Early Onset Inflammatory Bowel Disease.

Inflamm Bowel Dis 2017 12;23(12):2252-2255

*Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; †Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania; ‡Department of Biomedical Health Informatics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; §Department of Pediatrics, Division of Allergy and Immunology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; ‖Department of Pediatrics, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; ¶Department of Biostatistics and Epidemiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania; and **Department of Molecular Medicine, University of Rome Sapienza, Rome, Italy.

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http://dx.doi.org/10.1097/MIB.0000000000001280DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685903PMC
December 2017

Commentary on Mutations in Interleukin-10 Receptor and Clinical Phenotypes in Patients with Very Early-onset Inflammatory Bowel Disease: A Chinese VEO-IBD Collaboration Group Survey.

Inflamm Bowel Dis 2017 04;23(4):591-592

*Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; †Department of Biomedical Health Informatics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; ‡Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; §Department of Pediatrics, Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and ∥Department of Molecular Medicine, University Sapienza, Rome, Italy.

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http://dx.doi.org/10.1097/MIB.0000000000001028DOI Listing
April 2017

IQ and hemizygosity for the Val Met functional polymorphism of COMT in 22q11DS.

Am J Med Genet B Neuropsychiatr Genet 2016 12 13;171(8):1112-1115. Epub 2016 Sep 13.

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.b.32492DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733517PMC
December 2016

Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome.

Cell Mol Gastroenterol Hepatol 2016 Sep 26;2(5):663-675.e2. Epub 2016 May 26.

Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.

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https://linkinghub.elsevier.com/retrieve/pii/S2352345X163005
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http://dx.doi.org/10.1016/j.jcmgh.2016.05.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042888PMC
September 2016

Integration of Omics Data in Genetic Epidemiology.

Hum Hered 2015 28;79(3-4):109-10. Epub 2015 Jul 28.

INSERM UMR1078, CHU Brest, Université Bretagne Occidentale, Brest, France.

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http://search.proquest.com/openview/8f928e857ec313f9daabd485
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http://dx.doi.org/10.1159/000382041DOI Listing
April 2016

Compound heterozygous mutations in NEK8 in siblings with end-stage renal disease with hepatic and cardiac anomalies.

Am J Med Genet A 2016 Mar 24;170(3):750-3. Epub 2015 Dec 24.

Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, and The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.a.37512DOI Listing
March 2016

Polygenic inheritance of cryptorchidism susceptibility in the LE/orl rat.

Mol Hum Reprod 2016 Jan 26;22(1):18-34. Epub 2015 Oct 26.

Pediatric Urology Research Laboratory, Nemours Biomedical Research/Alfred I. duPont Hospital for Children, Wilmington, DE, USA.

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http://dx.doi.org/10.1093/molehr/gav060DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694052PMC
January 2016

Erratum to: A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.

BMC Gastroenterol 2015 Dec 18;15:179. Epub 2015 Dec 18.

Division of Human Genetics, The Children's Hospital of Philadelphia, Department of Pediatrics, Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania; Department of Molecular Medicine, University Sapienza, Rome, Italy.

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http://dx.doi.org/10.1186/s12876-015-0412-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683708PMC
December 2015

Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.

Gastroenterology 2015 Nov 17;149(6):1415-24. Epub 2015 Jul 17.

Division of Human Genetics, The Children's Hospital of Philadelphia; Department of Pediatrics, Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania; Department of Molecular Medicine, University Sapienza, Rome, Italy.

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http://dx.doi.org/10.1053/j.gastro.2015.07.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853027PMC
November 2015

A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.

BMC Gastroenterol 2015 Nov 18;15:160. Epub 2015 Nov 18.

Division of Human Genetics, The Children's Hospital of Philadelphia, Department of Pediatrics, Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania; Department of Molecular Medicine, University Sapienza, Rome, Italy.

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http://dx.doi.org/10.1186/s12876-015-0394-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652404PMC
November 2015

Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions.

Hum Reprod 2015 Oct 24;30(10):2439-51. Epub 2015 Jul 24.

Division of Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA Department of Molecular Medicine, Sapienza University, Rome, Italy.

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http://dx.doi.org/10.1093/humrep/dev180DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573451PMC
October 2015

Phenotype specific association of the TGFBR3 locus with nonsyndromic cryptorchidism.

J Urol 2015 May 25;193(5):1637-45. Epub 2014 Oct 25.

Division of Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Molecular Medicine, Sapienza University, Rome, Italy.

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http://dx.doi.org/10.1016/j.juro.2014.10.097DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4406821PMC
May 2015

Exome sequencing reveals compound heterozygous mutations in ATP8B1 in a JAG1/NOTCH2 mutation-negative patient with clinically diagnosed Alagille syndrome.

Am J Med Genet A 2015 Apr 3;167A(4):891-3. Epub 2015 Mar 3.

Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1002/ajmg.a.36946DOI Listing
April 2015

Common genetic variants in NEFL influence gene expression and neuroblastoma risk.

Cancer Res 2014 Dec 13;74(23):6913-24. Epub 2014 Oct 13.

Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania. Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania. Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania. Abramson Family Cancer Research Institute, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania. Genomics and Computational Biology, Biomedical Graduate Studies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1158/0008-5472.CAN-14-0431DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253722PMC
December 2014

Rare variants in TP53 and susceptibility to neuroblastoma.

J Natl Cancer Inst 2014 Apr 14;106(4):dju047. Epub 2014 Mar 14.

Affiliations of authors: Division of Oncology (SJD, MDi, DAO, KC, KRB, MRR, JMM), Center for Childhood Cancer Research (SJD, MDi, DAO, KC, KRB, MRR, JMM), Center for Applied Genomics (HH), and Division of Genetics (HH, MDe) Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics (SJD, DAO, KRB, HH, MDe, JMM), Abramson Cancer Center (SJD, JMM), Genomics and Computational Biology, Biomedical Graduate Studies (SJD, DAO, JMM), and Department of Biostatistics and Epidemiology (MDe), Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA (SJD, HH, MDe, JMM); Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Naples, Italy (MC, AI); Ceinge-Biotecnologie Avanzate, Naples, Italy (MC, AI); University of Rome "La Sapienza," Department of Molecular Medicine, Rome, Italy (MDe).

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http://jnci.oxfordjournals.org/content/early/2014/03/14/jnci
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http://jnci.oxfordjournals.org/cgi/doi/10.1093/jnci/dju047
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http://dx.doi.org/10.1093/jnci/dju047DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982892PMC
April 2014

Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia.

Hum Genet 2014 Feb 9;133(2):235-43. Epub 2013 Oct 9.

Genomics and Computational Biology Graduate Group, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA,

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http://dx.doi.org/10.1007/s00439-013-1368-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901047PMC
February 2014

Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus.

Am J Otolaryngol 2013 May-Jun;34(3):230-5. Epub 2013 Jan 29.

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

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http://dx.doi.org/10.1016/j.amjoto.2012.11.002DOI Listing
October 2013

Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.

Gastroenterology 2013 May 18;144(5):1107-1115.e3. Epub 2013 Jan 18.

Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.1053/j.gastro.2013.01.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736559PMC
May 2013

Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.

Nat Genet 2012 Oct 2;44(10):1126-30. Epub 2012 Sep 2.

Division of Oncology, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

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http://www.nature.com/articles/ng.2387
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http://dx.doi.org/10.1038/ng.2387DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459292PMC
October 2012

Genetic mapping of quantitative trait loci for disease-related phenotypes.

Methods Mol Biol 2012 ;871:281-311

Division of Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

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http://dx.doi.org/10.1007/978-1-61779-785-9_15DOI Listing
August 2012

Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.

Haematologica 2012 Jul 22;97(7):989-93. Epub 2012 Jan 22.

Clinica Pediatrica 2a, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Ospedale Regionale Microcitemie ASL8, Cagliari, Italy.

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http://dx.doi.org/10.3324/haematol.2011.053504DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396667PMC
July 2012

Next-generation linkage analysis.

Hum Hered 2011 23;72(4):227. Epub 2011 Dec 23.

Battelle Center for Mathematical Medicine, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.

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http://dx.doi.org/10.1159/000334421DOI Listing
April 2012

Replication of neuroblastoma SNP association at the BARD1 locus in African-Americans.

Cancer Epidemiol Biomarkers Prev 2012 Apr 10;21(4):658-63. Epub 2012 Feb 10.

Division of Human Genetics, The Children's Hospital of Philadelphia, 3615 Civic Center Blvd., Philadelphia, PA 19104, USA.

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http://cebp.aacrjournals.org/cgi/doi/10.1158/1055-9965.EPI-1
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http://dx.doi.org/10.1158/1055-9965.EPI-11-0830DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319325PMC
April 2012

Genome-wide linkage analysis to identify genetic modifiers of ALK mutation penetrance in familial neuroblastoma.

Hum Hered 2011 6;71(2):135-9. Epub 2011 Jul 6.

Division of Genetics, The Children's Hospital of Philadelphia, Pa., USA. devoto @ chop.edu

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http://dx.doi.org/10.1159/000324843DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136385PMC
January 2012

Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum.

Am J Med Genet B Neuropsychiatr Genet 2010 Sep;153B(6):1127-33

Department of Child and Adolescent Psychiatry, The Children's Hospital of Philadelphia, Science Center, 3440 Market Street, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.1002/ajmg.b.31110DOI Listing
September 2010

The Otto Aufranc Award: Identification of a 4 Mb region on chromosome 17q21 linked to developmental dysplasia of the hip in one 18-member, multigeneration family.

Clin Orthop Relat Res 2010 Feb 11;468(2):337-44. Epub 2009 Sep 11.

Thomas Jefferson University and the Rothman Institute of Orthopaedics, 925 Chestnut Street, 5th Floor, Philadelphia, PA 19107, USA.

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http://link.springer.com/10.1007/s11999-009-1073-6
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http://dx.doi.org/10.1007/s11999-009-1073-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807013PMC
February 2010

Incorporating prior biological information in linkage studies increases power and limits multiple testing.

BMC Proc 2007 18;1 Suppl 1:S89. Epub 2007 Dec 18.

Laboratorio di Genetica Molecolare, Istituto G, Gaslini, Largo G, Gaslini 5, 16148 Genova, Italy.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367562PMC
http://dx.doi.org/10.1186/1753-6561-1-s1-s89DOI Listing
December 2009

Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study.

BMC Proc 2009 Dec 15;3 Suppl 7:S93. Epub 2009 Dec 15.

The Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, Philadelphia, Pennsylvania 19104, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795997PMC
http://dx.doi.org/10.1186/1753-6561-3-s7-s93DOI Listing
December 2009

Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A.

Psychiatr Genet 2009 Jun;19(3):134-41

Department of Pediatrics, Division of Pulmonary Medicine, Center for Applied Genomics, The University of Pennsylvania, Philadelphia, Pennsylvania, USA.

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http://dx.doi.org/10.1097/YPG.0b013e32832a5043DOI Listing
June 2009

Identification of ALK as a major familial neuroblastoma predisposition gene.

Nature 2008 Oct 24;455(7215):930-5. Epub 2008 Aug 24.

Division of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

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http://dx.doi.org/10.1038/nature07261DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2672043PMC
October 2008

Variants of ST8SIA1 are associated with risk of developing multiple sclerosis.

PLoS One 2008 Jul 9;3(7):e2653. Epub 2008 Jul 9.

Institute of Genomic Medicine and Department of Pediatrics, UMDNJ-New Jersey Medical School, Newark, New Jersey, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0002653PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440423PMC
July 2008

Advances in family-based association analysis. Introduction.

Hum Hered 2008 31;66(2):65-6. Epub 2008 Mar 31.

Department of Genetics, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.

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http://dx.doi.org/10.1159/000119106DOI Listing
April 2008

ADHD genetics: 2007 update.

Curr Psychiatry Rep 2007 Oct;9(5):434-9

The Children's Hospital of Philadelphia, Science Center, 3440 Market Street, Philadelphia, PA 19104-6209, USA.

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October 2007

A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24.

Eur J Hum Genet 2007 Aug 9;15(8):889-97. Epub 2007 May 9.

Laboratory of Medical Genetics, Department of Internal Medicine, Cardioangiology and Hepatology, University of Bologna, Bologna, Italy.

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http://dx.doi.org/10.1038/sj.ejhg.5201844DOI Listing
August 2007

Genetic predisposition to familial neuroblastoma: identification of two novel genomic regions at 2p and 12p.

Hum Hered 2007 22;63(3-4):205-11. Epub 2007 Feb 22.

Unit of Translational Pediatric Oncology,National Institute for Cancer Research (IST), Genoa, Italy.

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http://dx.doi.org/10.1159/000099997DOI Listing
June 2007

Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota.

Mol Vis 2007 Feb 15;13:229-36. Epub 2007 Feb 15.

Division of Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633468PMC
February 2007

Ophthalmologic findings in Cornelia de Lange syndrome: a genotype-phenotype correlation study.

Arch Ophthalmol 2006 Apr;124(4):552-7

Division of Ophthalmology, The Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, USA.

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http://dx.doi.org/10.1001/archopht.124.4.552DOI Listing
April 2006

Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome.

Am J Med Genet A 2005 Sep;138(1):27-31

Division of Human Genetics and Molecular Biology, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

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http://dx.doi.org/10.1002/ajmg.a.30919DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2766539PMC
September 2005

Statistical tools for linkage analysis and genetic association studies.

Expert Rev Mol Diagn 2005 Sep;5(5):781-96

Istituto di Genetica delle Popolazioni - CNR, Alghero, Italy.

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http://dx.doi.org/10.1586/14737159.5.5.781DOI Listing
September 2005

Identification of a novel locus on 2q for autosomal dominant high-grade myopia.

Invest Ophthalmol Vis Sci 2005 Jul;46(7):2300-7

Divisions of Ophthalmology and.

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http://dx.doi.org/10.1167/iovs.04-1423DOI Listing
July 2005

Heterogeneity in the magnitude of the insulin gene effect on HLA risk in type 1 diabetes.

Diabetes 2004 Dec;53(12):3286-91

Dipartimento di Scienze Biomediche e Biotecnologie, Universita' di Cagliari, Sardinia, Italy.

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http://dx.doi.org/10.2337/diabetes.53.12.3286DOI Listing
December 2004

NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations.

Am J Hum Genet 2004 Oct 18;75(4):610-23. Epub 2004 Aug 18.

Division of Human Genetics and Molecular Biology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104-4318, USA.

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http://dx.doi.org/10.1086/424698DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182048PMC
October 2004

CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencing.

Clin Chem 2003 Oct;49(10):1675-9

Department of Medicine, Thomas Jefferson University, Jefferson Medical College, Philadelphia, PA 19104, USA.

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October 2003

New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.

Invest Ophthalmol Vis Sci 2003 May;44(5):1830-6

Division of Ophthalmology, Children's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

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http://dx.doi.org/10.1167/iovs.02-0697DOI Listing
May 2003

Weak linkage at 4p16 to predisposition for human neuroblastoma.

Oncogene 2002 Nov;21(54):8356-60

Laboratory of Neuroblastoma Research, Advanced Biotechnology Center, 16132 Genoa, Italy.

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http://dx.doi.org/10.1038/sj.onc.1206009DOI Listing
November 2002

Linkage analysis in families with recurrent neuroblastoma.

Ann N Y Acad Sci 2002 Jun;963:74-84

Laboratory of Neuroblastoma Research, Advanced Biotechnology Center, Genoa, Italy.

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http://dx.doi.org/10.1111/j.1749-6632.2002.tb04097.xDOI Listing
June 2002