Golder N Wilson

Golder N Wilson

UNVERIFIED PROFILE

Are you Golder N Wilson?   Register this Author

Register author
Golder N Wilson

Golder N Wilson

Publications by authors named "Golder N Wilson"

Are you Golder N Wilson?   Register this Author

26Publications

385Reads

28Profile Views

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.

Authors:
Pleuntje J van der Sluijs Sandra Jansen Samantha A Vergano Miho Adachi-Fukuda Yasemin Alanay Adila AlKindy Anwar Baban Allan Bayat Stefanie Beck-Wödl Katherine Berry Emilia K Bijlsma Levinus A Bok Alwin F J Brouwer Ineke van der Burgt Philippe M Campeau Natalie Canham Krystyna Chrzanowska Yoyo W Y Chu Brain H Y Chung Karin Dahan Marjan De Rademaeker Anne Destree Tracy Dudding-Byth Rachel Earl Nursel Elcioglu Ellen R Elias Christina Fagerberg Alice Gardham Blanca Gener Erica H Gerkes Ute Grasshoff Arie van Haeringen Karin R Heitink Johanna C Herkert Nicolette S den Hollander Denise Horn David Hunt Sarina G Kant Mitsuhiro Kato Hülya Kayserili Rogier Kersseboom Esra Kilic Malgorzata Krajewska-Walasek Kylin Lammers Lone W Laulund Damien Lederer Melissa Lees Vanesa López-González Saskia Maas Grazia M S Mancini Carlo Marcelis Francisco Martinez Isabelle Maystadt Marianne McGuire Shane McKee Sarju Mehta Kay Metcalfe Jeff Milunsky Seiji Mizuno John B Moeschler Christian Netzer Charlotte W Ockeloen Barbara Oehl-Jaschkowitz Nobuhiko Okamoto Sharon N M Olminkhof Carmen Orellana Laurent Pasquier Caroline Pottinger Vera Riehmer Stephen P Robertson Maian Roifman Caroline Rooryck Fabienne G Ropers Monica Rosello Claudia A L Ruivenkamp Mahmut S Sagiroglu Suzanne C E H Sallevelt Amparo Sanchis Calvo Pelin O Simsek-Kiper Gabriela Soares Lucia Solaeche Fatma Mujgan Sonmez Miranda Splitt Duco Steenbeek Alexander P A Stegmann Constance T R M Stumpel Saori Tanabe Eyyup Uctepe G Eda Utine Hermine E Veenstra-Knol Sunita Venkateswaran Catheline Vilain Catherine Vincent-Delorme Anneke T Vulto-van Silfhout Patricia Wheeler Golder N Wilson Louise C Wilson Bernd Wollnik Tomoki Kosho Dagmar Wieczorek Evan Eichler Rolph Pfundt Bert B A de Vries Jill Clayton-Smith Gijs W E Santen

Genet Med 2019 Sep;21(9):2160-2161

Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41436-018-0368-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752317PMC
September 2019

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.

Authors:
Pleuntje J van der Sluijs Sandra Jansen Samantha A Vergano Miho Adachi-Fukuda Yasemin Alanay Adila AlKindy Anwar Baban Allan Bayat Stefanie Beck-Wödl Katherine Berry Emilia K Bijlsma Levinus A Bok Alwin F J Brouwer Ineke van der Burgt Philippe M Campeau Natalie Canham Krystyna Chrzanowska Yoyo W Y Chu Brain H Y Chung Karin Dahan Marjan De Rademaeker Anne Destree Tracy Dudding-Byth Rachel Earl Nursel Elcioglu Ellen R Elias Christina Fagerberg Alice Gardham Blanca Gener Erica H Gerkes Ute Grasshoff Arie van Haeringen Karin R Heitink Johanna C Herkert Nicolette S den Hollander Denise Horn David Hunt Sarina G Kant Mitsuhiro Kato Hülya Kayserili Rogier Kersseboom Esra Kilic Malgorzata Krajewska-Walasek Kylin Lammers Lone W Laulund Damien Lederer Melissa Lees Vanesa López-González Saskia Maas Grazia M S Mancini Carlo Marcelis Francisco Martinez Isabelle Maystadt Marianne McGuire Shane McKee Sarju Mehta Kay Metcalfe Jeff Milunsky Seiji Mizuno John B Moeschler Christian Netzer Charlotte W Ockeloen Barbara Oehl-Jaschkowitz Nobuhiko Okamoto Sharon N M Olminkhof Carmen Orellana Laurent Pasquier Caroline Pottinger Vera Riehmer Stephen P Robertson Maian Roifman Caroline Rooryck Fabienne G Ropers Monica Rosello Claudia A L Ruivenkamp Mahmut S Sagiroglu Suzanne C E H Sallevelt Amparo Sanchis Calvo Pelin O Simsek-Kiper Gabriela Soares Lucia Solaeche Fatma Mujgan Sonmez Miranda Splitt Duco Steenbeek Alexander P A Stegmann Constance T R M Stumpel Saori Tanabe Eyyup Uctepe G Eda Utine Hermine E Veenstra-Knol Sunita Venkateswaran Catheline Vilain Catherine Vincent-Delorme Anneke T Vulto-van Silfhout Patricia Wheeler Golder N Wilson Louise C Wilson Bernd Wollnik Tomoki Kosho Dagmar Wieczorek Evan Eichler Rolph Pfundt Bert B A de Vries Jill Clayton-Smith Gijs W E Santen

Genet Med 2019 06 8;21(6):1295-1307. Epub 2018 Nov 8.

Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://www.nature.com/articles/s41436-018-0330-z
Publisher Site
http://dx.doi.org/10.1038/s41436-018-0330-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752273PMC
June 2019

KCNK9 imprinting syndrome-further delineation of a possible treatable disorder.

Am J Med Genet A 2016 10 6;170(10):2632-7. Epub 2016 May 6.

Genetic Institute, Emek Medical Center, Afula, Israel.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.37740DOI Listing
October 2016

Chromosome Xq13.2 Microduplication Involving an X-Inactivation Gene in a Girl with Short Stature, Madelung Deformity, and von Willebrand Disease.

J Pediatr Adolesc Gynecol 2016 Apr 27;29(2):e39-42. Epub 2015 Nov 27.

Department of Pediatrics, Texas Tech University Health Science Center, Lubbock, Texas.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jpag.2015.11.010DOI Listing
April 2016

Inaccuracy of non-invasive prenatal screening demands cautious counsel and follow-up.

Am J Med Genet A 2016 Apr 28;170A(4):1086-7. Epub 2015 Dec 28.

Department of Pediatrics, Texas Tech University Health Science Center, Lubbock and Medical City Hospital, Dallas, Texas.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.37530DOI Listing
April 2016

Registry analysis supports different mechanisms for gastroschisis and omphalocele within shared developmental fields.

Am J Med Genet A 2015 Nov 2;167A(11):2568-81. Epub 2015 Jul 2.

Department of Pediatrics, Texas Tech University Health Science Center, Lubbock and Medical City Hospital, Dallas, Texas.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.37236DOI Listing
November 2015

Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delay.

Am J Med Genet A 2015 Apr 3;167A(4):695-700. Epub 2015 Mar 3.

Indiana University School of Medicine-Northwest, Genetics Center, Gary, Indiana.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajmg.a.36956
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.36956DOI Listing
April 2015

Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.

Am J Hum Genet 2015 Mar 26;96(3):507-13. Epub 2015 Feb 26.

Department of Clinical Genetics, Karolinska University Hospital, 171 76 Stockholm, Sweden; Department of Molecular Medicine and Surgery, Karolinska Institutet, 171 76 Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2015.01.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375419PMC
March 2015

Exome analysis of connective tissue dysplasia: death and rebirth of clinical genetics?

Authors:
Golder N Wilson

Am J Med Genet A 2014 May 24;164A(5):1209-12. Epub 2014 Mar 24.

Departments of Pediatrics, Obstetrics and Gynecology, Texas Tech University Health Science Centers, Amarillo and Lubbock (Pediatrics), KinderGenome Pediatric Genetics, Dallas, Texas.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.36463DOI Listing
May 2014

Presymptomatic and preimplantation genetic diagnosis: neurology, NextGenetics, and the next generation.

Authors:
Golder N Wilson

JAMA Neurol 2014 Apr;71(4):403-4

Texas Tech University Health Science Centers, Amarillo, Texas2Texas Tech University Health Science Centers, Lubbock, Texas3KinderGenome Pediatric Genetics, Medical City Hospital, Dallas, Texas.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamaneurol.2013.5834DOI Listing
April 2014

Anomalies associated with gastroschisis and omphalocele: analysis of 2825 cases from the Texas Birth Defects Registry.

J Pediatr Surg 2014 Apr 18;49(4):514-9. Epub 2013 Nov 18.

Pediatric Genetics, Departments of Pediatrics, Obstetrics & Gynecology, Texas Tech University Health Science Center, Amarillo and Lubbock (Pediatrics), Amarillo, TX 79106, USA.

View Article

Download full-text PDF

Source
http://lib.ajaums.ac.ir/booklist/1-s2.0-S0022346813009135-ma
Web Search
http://dx.doi.org/10.1016/j.jpedsurg.2013.11.052DOI Listing
April 2014

Measure radiation exposure and sensitivity.

Authors:
Golder N Wilson

JAMA Pediatr 2014 Feb;168(2):187-8

Department of Pediatrics, Texas Tech University Health Science Centers, Amarillo and Lubbock.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamapediatrics.2013.4662DOI Listing
February 2014

The MEF2C gene-microdeletion 5q14.3 dilemma and three axioms for molecular syndromology.

Authors:
Golder N Wilson

Am J Med Genet A 2013 Apr 12;161A(4):916-7. Epub 2013 Mar 12.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.35785DOI Listing
April 2013

Maternal genetic effect in DNA analysis: egg on your traits.

Authors:
Golder N Wilson

Am J Med Genet A 2012 Jul 31;158A(7):1589-93. Epub 2012 May 31.

Pediatrics, Obstetrics and Gynecology, Texas Tech University Health Science Centers, Dallas, Texas 75209, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.35407DOI Listing
July 2012

Interstitial deletion 5q14.3q21.3 with MEF2C haploinsufficiency and mild phenotype: when more is less.

Am J Med Genet A 2011 Jun 12;155A(6):1437-41. Epub 2011 May 12.

Department of Pediatrics, Texas Tech University Health Science Center, Lubbock, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.34012DOI Listing
June 2011

Genetic drift. Saving Grace: On the nature of syndromes and the missed Nobel.

Authors:
Golder N Wilson

Am J Med Genet A 2011 Mar 22;155A(3):466-8. Epub 2011 Feb 22.

Texas Tech University Health Science Centers, Amarillo and Lubbock, KinderGenome Pediatric Genetics, Dallas, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33854DOI Listing
March 2011

A user's guide to the elements of standard morphologic terminology: Analysis and database.

Authors:
Golder N Wilson

Am J Med Genet A 2010 Jul;152A(7):1627-9

Department of Pediatrics, Texas Tech University Health Science Centers, Amarillo and Lubbock, KinderGenome Private Practice, Dallas, Texas 75209, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33422DOI Listing
July 2010

Al-Awadi/Raas-Rothschild/Schinzel (AARRS) phocomelia syndrome: case report and developmental field analysis.

Am J Med Genet A 2009 Jul;149A(7):1494-8

Department of Pediatrics, Texas Tech Health Sciences Center at Amarillo, Amarillo, Texas 75209, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.32890DOI Listing
July 2009

A need for pediatric genetics.

Authors:
Golder N Wilson

Arch Pediatr Adolesc Med 2007 Oct;161(10):1010

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archpedi.161.10.1010-aDOI Listing
October 2007

Tales from the neural genome: the lessons of homozygous porphyria.

Authors:
Golder N Wilson

Arch Neurol 2004 Nov;61(11):1650-1

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.61.11.1650DOI Listing
November 2004

Biochemical abnormality associated with Smith-Lemli-Opitz syndrome in an infant with features of Rutledge multiple congenital anomaly syndrome confirms that the latter is a variant of the former.

Pediatr Dev Pathol 2003 May-Jun;6(3):270-7. Epub 2003 Apr 30.

Department of Pathology, Mail Code 9073, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10024-002-1116-4DOI Listing
December 2003

Behavioral assessment of children with Down syndrome using the Reiss psychopathology scale.

Am J Med Genet A 2003 Apr;118A(3):210-6

Children's Medical Center of Dallas and the Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas TX 75390-9063, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.20007DOI Listing
April 2003

Coming together for blastogenesis.

Authors:
Golder N Wilson

Am J Med Genet A 2003 Mar;117A(3):309

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.10033DOI Listing
March 2003