Jeffrey Gruen

Jeffrey Gruen

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Jeffrey Gruen

Jeffrey Gruen

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Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes.

Child Neuropsychol 2019 Aug 14:1-25. Epub 2019 Aug 14.

e Department of Child and Youth Studies, Brock University , St. Catharines , Ontario , Canada.

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http://dx.doi.org/10.1080/09297049.2019.1648642DOI Listing
August 2019

Genetics of bronchopulmonary dysplasia: When things do not match up, it is only the beginning.

J Pediatr 2019 May 6;208:298-299. Epub 2019 Feb 6.

Department of Pediatrics, Division of Neonatology, Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1016/j.jpeds.2019.01.014DOI Listing
May 2019

A method for integrating neuroimaging into genetic models of learning performance.

Genet Epidemiol 2017 Jan 18;41(1):4-17. Epub 2016 Nov 18.

Department of Biostatistics, Yale University, New Haven, CT, USA.

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http://dx.doi.org/10.1002/gepi.22025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154929PMC
January 2017

Gray matter maturation and cognition in children with different APOE ε genotypes.

Neurology 2016 Aug 13;87(6):585-94. Epub 2016 Jul 13.

From the Department of Medicine (L.C., V.D., K.L., A.P., T.E.), John A. Burns School of Medicine, University of Hawaii and The Queen's Medical Center, Honolulu; Department of Psychiatry, School of Medicine (C.B.), Departments of Psychiatry and Cognitive Science (T.L.J., N.A.), and Department of Pathology (S.S.M.), University of California San Diego, La Jolla; Department of Psychiatry (J.F., D.N.K.), University of Massachusetts Medical School, Boston; Department of Psychiatry and Behavioral Sciences (D.G.A.), University of California, Davis; Departments of Pediatrics and Investigative Medicine (J.G.), Yale Child Health Research Center, Yale University School of Medicine, New Haven, CT; Boston Children's Hospital (W.E.K.), Harvard Medical School, Boston, MA; Sackler Institute for Developmental Psychobiology (B.J.C.), Weil Cornell Medical College, New York, NY; Department of Pediatrics (E.S.), University of Southern California, Los Angeles; and Children's Hospital (E.S.), Los Angeles, CA.

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http://www.neurology.org/content/early/2016/07/13/WNL.000000
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http://dx.doi.org/10.1212/WNL.0000000000002939DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977368PMC
August 2016

The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.

J Med Genet 2016 Mar 11;53(3):163-71. Epub 2015 Dec 11.

Investigate Medicine, Yale University, New Haven, Connecticut, USA Department of Pediatrics, Yale University, New Haven, Connecticut, USA Department of Investigative Medicine, Yale University, New Haven, Connecticut, USA.

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http://dx.doi.org/10.1136/jmedgenet-2015-103418DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789805PMC
March 2016

The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.

Neuroimage 2016 Jan 1;124(Pt B):1149-1154. Epub 2015 May 1.

Department of Cognitive Science, University of California, San Diego, La Jolla, CA, USA; Multimodal Imaging Laboratory, University of California, San Diego, La Jolla, CA, USA; Department of Neurosciences, University of California, San Diego, La Jolla, CA, USA; Department of Radiology, University of California, San Diego, La Jolla, CA, USA.

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http://dx.doi.org/10.1016/j.neuroimage.2015.04.057DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628902PMC
January 2016

What is the basis for a genetic approach in neonatal disorders?

Semin Perinatol 2015 Dec 23;39(8):568-73. Epub 2015 Oct 23.

Division of Perinatal Medicine, Department of Pediatrics, Yale University School of Medicine, New Haven, CT; Yale Child Health Research Center, Department of Pediatrics, Yale University School of Medicine, New Haven, CT; Department of Genetics, Yale University School of Medicine, New Haven, CT; Department of Investigative Medicine, Yale University School of Medicine, New Haven, CT.

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https://linkinghub.elsevier.com/retrieve/pii/S01460005150012
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http://dx.doi.org/10.1053/j.semperi.2015.09.003DOI Listing
December 2015

Family income, parental education and brain structure in children and adolescents.

Nat Neurosci 2015 May 30;18(5):773-8. Epub 2015 Mar 30.

1] The Saban Research Institute of Children's Hospital, Los Angeles, California, USA. [2] Department of Pediatrics of the Keck School of Medicine, University of Southern California, Los Angeles, California, USA. [3] The Pediatric Imaging, Neurocognition, and Genetics Study, San Diego, California, USA.

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http://www.columbia.edu/cu/needlab/Publications/PING%20Natur
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http://www.nature.com/doifinder/10.1038/nn.3983
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http://dx.doi.org/10.1038/nn.3983DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4414816PMC
May 2015

Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.

Autism Res 2015 Apr 1;8(2):229-34. Epub 2014 Dec 1.

Department of Genetics, Yale University, New Haven, Connecticut.

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http://dx.doi.org/10.1002/aur.1436DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412753PMC
April 2015

The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.

Cortex 2014 Aug 9;57:227-43. Epub 2014 May 9.

C.E.R.M.A.C. (Centro di Risonanza Magnetica ad Alto Campo), Milan, Italy; Department of Nuclear Medicine San Raffaele Hospital and Division of Neuroscience, Scientific Institute San Raffaele, Milan, Italy; Vita-Salute San Raffaele University, Milan, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00109452140013
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http://dx.doi.org/10.1016/j.cortex.2014.04.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975637PMC
August 2014

Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.

Mol Genet Metab 2013 Nov 17;110(3):201-12. Epub 2013 Jul 17.

Department of Genetics, Yale University School of Medicine, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1016/j.ymgme.2013.07.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800223PMC
November 2013

Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.

Am J Hum Genet 2013 Jul 6;93(1):19-28. Epub 2013 Jun 6.

Department of Genetics, Yale University, 464 Congress Avenue, Suite 243, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1016/j.ajhg.2013.05.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3710765PMC
July 2013

Prenatal exposure to nicotine and impaired reading performance.

J Pediatr 2013 Apr 2;162(4):713-718.e2. Epub 2012 Nov 2.

Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1016/j.jpeds.2012.09.041DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3577994PMC
April 2013

Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.

Authors:
Trygve E Bakken J Cooper Roddey Srdjan Djurovic Natacha Akshoomoff David G Amaral Cinnamon S Bloss B J Casey Linda Chang Thomas M Ernst Jeffrey R Gruen Terry L Jernigan Walter E Kaufmann Tal Kenet David N Kennedy Joshua M Kuperman Sarah S Murray Elizabeth R Sowell Lars M Rimol Morten Mattingsdal Ingrid Melle Ingrid Agartz Ole A Andreassen Nicholas J Schork Anders M Dale Michael Weiner Paul Aisen Ronald Petersen Clifford R Jack William Jagust John Q Trojanowki Arthur W Toga Laurel Beckett Robert C Green Andrew J Saykin John Morris Enchi Liu Tom Montine Anthony Gamst Ronald G Thomas Michael Donohue Sarah Walter Devon Gessert Tamie Sather Danielle Harvey John Kornak Anders Dale Matthew Bernstein Joel Felmlee Nick Fox Paul Thompson Norbert Schuff Gene Alexander Charles DeCarli Dan Bandy Robert A Koeppe Norm Foster Eric M Reiman Kewei Chen Chet Mathis Nigel J Cairns Lisa Taylor-Reinwald J Q Trojanowki Les Shaw Virginia M Y Lee Magdalena Korecka Karen Crawford Scott Neu Tatiana M Foroud Steven Potkin Li Shen Zaven Kachaturian Richard Frank Peter J Snyder Susan Molchan Jeffrey Kaye Joseph Quinn Betty Lind Sara Dolen Lon S Schneider Sonia Pawluczyk Bryan M Spann James Brewer Helen Vanderswag Judith L Heidebrink Joanne L Lord Kris Johnson Rachelle S Doody Javier Villanueva-Meyer Munir Chowdhury Yaakov Stern Lawrence S Honig Karen L Bell John C Morris Beau Ances Maria Carroll Sue Leon Mark A Mintun Stacy Schneider Daniel Marson Randall Griffith David Clark Hillel Grossman Effie Mitsis Aliza Romirowsky Leyla deToledo-Morrell Raj C Shah Ranjan Duara Daniel Varon Peggy Roberts Marilyn Albert Chiadi Onyike Stephanie Kielb Henry Rusinek Mony J de Leon Lidia Glodzik Susan De Santi P Murali Doraiswamy Jeffrey R Petrella R Edward Coleman Steven E Arnold Jason H Karlawish David Wolk Charles D Smith Greg Jicha Peter Hardy Oscar L Lopez MaryAnn Oakley Donna M Simpson Anton P Porsteinsson Bonnie S Goldstein Kim Martin Kelly M Makino M Saleem Ismail Connie Brand Ruth A Mulnard Gaby Thai Catherine Mc-Adams-Ortiz Kyle Womack Dana Mathews Mary Quiceno Ramon Diaz-Arrastia Richard King Myron Weiner Kristen Martin-Cook Michael DeVous Allan I Levey James J Lah Janet S Cellar Jeffrey M Burns Heather S Anderson Russell H Swerdlow Liana Apostolova Po H Lu George Bartzokis Daniel H S Silverman Neill R Graff-Radford Francine Parfitt Heather Johnson Martin R Farlow Ann Marie Hake Brandy R Matthews Scott Herring Christopher H van Dyck Richard E Carson Martha G MacAvoy Howard Chertkow Howard Bergman Chris Hosein Sandra Black Bojana Stefanovic Curtis Caldwell Ging-Yuek Robin Hsiung Howard Feldman Benita Mudge Michele Assaly Andrew Kertesz John Rogers Dick Trost Charles Bernick Donna Munic Diana Kerwin Marek-Marsel Mesulam Kristina Lipowski Chuang-Kuo Wu Nancy Johnson Carl Sadowsky Walter Martinez Teresa Villena Raymond Scott Turner Kathleen Johnson Brigid Reynolds Reisa A Sperling Keith A Johnson Gad Marshall Meghan Frey Jerome Yesavage Joy L Taylor Barton Lane Allyson Rosen Jared Tinklenberg Marwan Sabbagh Christine Belden Sandra Jacobson Neil Kowall Ronald Killiany Andrew E Budson Alexander Norbash Patricia Lynn Johnson Thomas O Obisesan Saba Wolday Salome K Bwayo Alan Lerner Leon Hudson Paula Ogrocki Evan Fletcher Owen Carmichael John Olichney Smita Kittur Michael Borrie T-Y Lee Rob Bartha Sterling Johnson Sanjay Asthana Cynthia M Carlsson Steven G Potkin Adrian Preda Dana Nguyen Pierre Tariot Adam Fleisher Stephanie Reeder Vernice Bates Horacio Capote Michelle Rainka Douglas W Scharre Maria Kataki Earl A Zimmerman Dzintra Celmins Alice D Brown Godfrey D Pearlson Karen Blank Karen Anderson Robert B Santulli Eben S Schwartz Kaycee M Sink Jeff D Williamson Pradeep Garg Franklin Watkins Brian R Ott Henry Querfurth Geoffrey Tremont Stephen Salloway Paul Malloy Stephen Correia Howard J Rosen Bruce L Miller Jacobo Mintzer Crystal Flynn Longmire Kenneth Spicer Elizabether Finger Irina Rachinsky Dick Drost Terry Jernigan Connor McCabe Ellen Grant Thomas Ernst Josh Kuperman Yoon Chung Sarah Murray Cinnamon Bloss Burcu Darst Lexi Pritchett Ashley Saito David Amaral Mishaela DiNino Bella Eyngorina Elizabeth Sowell Suzanne Houston Lindsay Soderberg Walter Kaufmann Peter van Zijl Hilda Rizzo-Busack Mohsin Javid Natasha Mehta Erika Ruberry Alisa Powers Bruce Rosen Nitzah Gebhard Holly Manigan Jean Frazier David Kennedy Lauren Yakutis Michael Hill Jeffrey Gruen Joan Bosson-Heenan Heatherly Carlson

Proc Natl Acad Sci U S A 2012 Mar 16;109(10):3985-90. Epub 2012 Feb 16.

Medical Scientist Training Program, University of California at San Diego, La Jolla, CA 92093, USA.

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http://dx.doi.org/10.1073/pnas.1105829109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309762PMC
March 2012

DCDC2 genetic variants and susceptibility to developmental dyslexia.

Psychiatr Genet 2012 Feb;22(1):25-30

Department of Child Psychiatry, Scientific Institute Eugenio Medea, Bosisio Parini, Italy.

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http://dx.doi.org/10.1097/YPG.0b013e32834acdb2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232293PMC
February 2012

A highly sensitive, high-throughput assay for the detection of Turner syndrome.

J Clin Endocrinol Metab 2011 Mar 22;96(3):699-705. Epub 2010 Dec 22.

Yale Child Health Research Center, Yale University School of Medicine, 464 Congress Avenue, New Haven, Connecticut 06520, USA.

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http://dx.doi.org/10.1210/jc.2010-1554DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3047225PMC
March 2011

The impact of environmental and genetic factors on neonatal late-onset sepsis.

J Pediatr 2011 Feb 17;158(2):234-8.e1. Epub 2010 Sep 17.

Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520-8064, USA.

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http://dx.doi.org/10.1016/j.jpeds.2010.07.060DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008342PMC
February 2011

A dyslexia-associated variant in DCDC2 changes gene expression.

Behav Genet 2011 Jan 2;41(1):58-66. Epub 2010 Nov 2.

Department of Pediatrics, Yale Child Health Research Center, Yale University School of Medicine, 464 Congress Avenue, New Haven, CT 06520-8081, USA.

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http://link.springer.com/10.1007/s10519-010-9408-3
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http://dx.doi.org/10.1007/s10519-010-9408-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053575PMC
January 2011

Progress towards a cellular neurobiology of reading disability.

Neurobiol Dis 2010 May 17;38(2):173-80. Epub 2009 Jul 17.

Department of Psychology, Lafayette College, Easton, PA, USA.

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http://dx.doi.org/10.1016/j.nbd.2009.06.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854314PMC
May 2010

Functional impact of a single-nucleotide polymorphism in the OPRD1 promoter region.

J Hum Genet 2010 May 19;55(5):278-84. Epub 2010 Mar 19.

Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.

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http://dx.doi.org/10.1038/jhg.2010.22DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876206PMC
May 2010

The genetic susceptibility to respiratory distress syndrome.

Pediatr Res 2009 Dec;66(6):693-7

Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut 06520, USA.

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http://dx.doi.org/10.1203/PDR.0b013e3181bbce86DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796284PMC
December 2009

Cognitive flexibility is associated with KIBRA variant and modulated by recent tobacco use.

Neuropsychopharmacology 2009 Nov 15;34(12):2508-16. Epub 2009 Jul 15.

Division of Human Genetics, Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06516, USA.

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http://dx.doi.org/10.1038/npp.2009.80DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2898508PMC
November 2009

Genetic contribution to patent ductus arteriosus in the premature newborn.

Pediatrics 2009 Feb;123(2):669-73

Yale University School of Medicine, Department of Pediatrics, 333 Cedar St, PO Box 208064, New Haven, CT 06520-8064, USA.

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http://dx.doi.org/10.1542/peds.2008-1117DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161726PMC
February 2009

Haplotypic variants in DRD2, ANKK1, TTC12, and NCAM1 are associated with comorbid alcohol and drug dependence.

Alcohol Clin Exp Res 2008 Dec 30;32(12):2117-27. Epub 2008 Sep 30.

Department of Psychiatry, Division of Human Genetics, Yale University School of Medicine, New Haven, Connecticut 06516, USA.

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http://doi.wiley.com/10.1111/j.1530-0277.2008.00800.x
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http://dx.doi.org/10.1111/j.1530-0277.2008.00800.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975565PMC
December 2008

The human lexinome: genes of language and reading.

J Commun Disord 2008 Sep-Oct;41(5):409-20. Epub 2008 Mar 25.

Department of Pediatrics, Yale Child Health Research Center, Yale University School of Medicine, New Haven, CT 06520-8081, USA.

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http://dx.doi.org/10.1016/j.jcomdis.2008.03.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2488410PMC
October 2008

Association of haplotypic variants in DRD2, ANKK1, TTC12 and NCAM1 to alcohol dependence in independent case control and family samples.

Hum Mol Genet 2007 Dec 30;16(23):2844-53. Epub 2007 Aug 30.

Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/ddm240DOI Listing
December 2007

Guideline for data analysis of genomewide association studies.

Cancer Genomics Proteomics 2007 Jan-Feb;4(1):27-34

Yale University School of Medicine, New Haven, CT 06520-8034, USA.

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October 2007

Management of dyslexia, its rationale, and underlying neurobiology.

Pediatr Clin North Am 2007 Jun;54(3):609-23, viii

Department of Pediatrics, Division of Child Neurology, Yale University School of Medicine, PO Box 333, New Haven, CT 06510-8064, USA.

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http://dx.doi.org/10.1016/j.pcl.2007.02.013DOI Listing
June 2007

Genetic approaches to complications of prematurity.

Front Biosci 2007 Jan 1;12:2344-51. Epub 2007 Jan 1.

Department of Pediatrics, Yale Child Health Research Center, Yale University School of Medicine, 464 Congress Avenue, New Haven, CT 06520, USA.

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http://dx.doi.org/10.2741/2236DOI Listing
January 2007

Genetic susceptibility to retinopathy of prematurity.

Pediatrics 2006 Nov;118(5):1858-63

Department of Pediatrics, Yale University School of Medicine, 333 Cedar St, New Haven, CT 06520-8064, USA.

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http://dx.doi.org/10.1542/peds.2006-1088DOI Listing
November 2006

The genetics of bronchopulmonary dysplasia.

Semin Perinatol 2006 Aug;30(4):185-91

Division of Perinatal Medicine and Yale Child Health Research Center, Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1053/j.semperi.2006.05.005DOI Listing
August 2006

Familial and genetic susceptibility to major neonatal morbidities in preterm twins.

Pediatrics 2006 Jun;117(6):1901-6

Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520-8064, USA.

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http://dx.doi.org/10.1542/peds.2005-1414DOI Listing
June 2006

Opinions on DM outcomes can be swayed.

Manag Care 2006 Jun;15(6):41-3

Revolution Health Group, USA.

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June 2006

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort.

Hum Genet 2005 Oct 28;118(1):87-90. Epub 2005 Oct 28.

Department of Pediatrics, Yale Child Health Research Center, Yale University School of Medicine, 464 Congress Avenue, New Haven, CT 06520-8081, USA.

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http://dx.doi.org/10.1007/s00439-005-0017-9DOI Listing
October 2005

CAT 53: a protein phosphatase 1 nuclear targeting subunit encoded in the MHC Class I region strongly expressed in regions of the brain involved in memory, learning, and Alzheimer's disease.

Brain Res Mol Brain Res 2005 Jul;138(1):70-83

Cambridge Centre for Brain Repair, Department of Clinical Neuroscience, University of Cambridge, Forvie Site, Robinson Way, Cambridge CB2 2PY, UK.

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http://dx.doi.org/10.1016/j.molbrainres.2005.04.001DOI Listing
July 2005

Detection of Turner syndrome using high-throughput quantitative genotyping.

J Clin Endocrinol Metab 2005 Jun 29;90(6):3419-22. Epub 2005 Mar 29.

Section of Perinatal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520, USA.

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http://dx.doi.org/10.1210/jc.2005-0544DOI Listing
June 2005

Prss16 is not required for T-cell development.

Mol Cell Biol 2005 Jan;25(2):789-96

Division of Gastroenterology, Department of Internal Medicine, UC Davis Medical Center, 4150 V St., PSSB 3500, Sacramento, CA 95817, USA.

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http://dx.doi.org/10.1128/MCB.25.2.789-796.2005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC543420PMC
January 2005

Seven new cases of familial isolated bladder exstrophy and epispadias complex (BEEC) and review of the literature.

Am J Med Genet A 2003 Jul;120A(2):215-21

Department of Pediatrics, Children's Hospital, Medical Center of the University of Bonn, Adenauerallee, Bonn, Germany.

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http://dx.doi.org/10.1002/ajmg.a.20057DOI Listing
July 2003

A transcription map of the 6p22.3 reading disability locus identifying candidate genes.

BMC Genomics 2003 Jun 30;4(1):25. Epub 2003 Jun 30.

Graduate Program in Genetics, State University of New York at Stony Brook, NY, USA.

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http://dx.doi.org/10.1186/1471-2164-4-25DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC166143PMC
June 2003

A detailed physical map of the 6p reading disability locus, including new markers and confirmation of recombination suppression.

Hum Genet 2002 Oct 13;111(4-5):339-49. Epub 2002 Aug 13.

Department of Genome Research, DNA Research Institute, Bioneer Corporation, Cheongwon-Kun, Chungbuk 363-813, Republic of Korea.

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http://dx.doi.org/10.1007/s00439-002-0771-xDOI Listing
October 2002

Expression, genomic structure and mapping of the thymus specific protease prss16: a candidate gene for insulin dependent diabetes mellitus susceptibility.

J Autoimmun 2002 Jun;18(4):311-6

Division of Gastroenterology, Department of Internal Medicine, University of California Davis, Davis, CA 95817, USA.

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June 2002