Publications by authors named "Jorieke E H Bergman"

41Publications

Maternal risk associated with the VACTERL association: A case-control study.

Birth Defects Res 2020 Nov 22;112(18):1495-1504. Epub 2020 Jul 22.

Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, the Netherlands.

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http://dx.doi.org/10.1002/bdr2.1773DOI Listing
November 2020

Etiological diagnosis in limb reduction defects and the number of affected limbs: A population-based study in the Northern Netherlands.

Am J Med Genet A 2020 Dec 21;182(12):2909-2918. Epub 2020 Sep 21.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.61875DOI Listing
December 2020

Maternal occupational exposure to solvents and gastroschisis in offspring - National Birth Defects Prevention Study 1997-2011.

Occup Environ Med 2020 03 16;77(3):172-178. Epub 2020 Jan 16.

National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, United States.

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http://dx.doi.org/10.1136/oemed-2019-106147DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035687PMC
March 2020

Prenatal diagnosis of urinary tract anomalies, a cohort study in the Northern Netherlands.

Prenat Diagn 2018 01 4;38(2):130-134. Epub 2018 Jan 4.

Eurocat Northern Netherlands, Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/pd.5200DOI Listing
January 2018

Maternal occupational exposure and oral clefts in offspring.

Environ Health 2017 08 4;16(1):83. Epub 2017 Aug 4.

Department of Genetics, University of Groningen, University Medical Center Groningen, HPC CB 51, P.O. Box 30.001, 9700 RB, Groningen, the Netherlands.

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http://dx.doi.org/10.1186/s12940-017-0294-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545025PMC
August 2017

Prenatal exposure to serotonin reuptake inhibitors and congenital heart anomalies: an exploratory pharmacogenetics study.

Pharmacogenomics 2017 Jul 22;18(10):987-1001. Epub 2017 Jun 22.

Unit of PharmacoTherapy, -Epidemiology & -Economics, Department of Pharmacy, University of Groningen, Groningen Research Institute of Pharmacy, Groningen, The Netherlands.

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http://dx.doi.org/10.2217/pgs-2017-0036DOI Listing
July 2017

Impact of Muscarinic M Receptor Antagonism on the Risk of Type 2 Diabetes in Antidepressant-Treated Patients: A Case-Controlled Study.

CNS Drugs 2017 Jun;31(6):483-493

Unit of PharmacoTherapy, -Epidemiology & -Economics, Groningen Research Institute of Pharmacy, University of Groningen, Antonius Deusinglaan 1, 9713 AV, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s40263-017-0436-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488147PMC
June 2017

Knowledge and attitude regarding pharmacogenetics among formerly pregnant women in the Netherlands and their interest in pharmacogenetic research.

BMC Pregnancy Childbirth 2017 04 14;17(1):120. Epub 2017 Apr 14.

Department of Pharmacy, University of Groningen, Groningen Research Institute of Pharmacy, Unit of PharmacoTherapy, -Epidemiology & -Economics, 9713AV, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/s12884-017-1290-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5391584PMC
April 2017

Exposure to reactive intermediate-inducing drugs during pregnancy and the incident use of psychotropic medications among children.

Pharmacoepidemiol Drug Saf 2017 Mar 18;26(3):265-273. Epub 2017 Jan 18.

Groningen Research Institute of Pharmacy, Unit of Pharmacotherapy, Epidemiology and Economics, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/pds.4161DOI Listing
March 2017

The Risk of Congenital Heart Anomalies Following Prenatal Exposure to Serotonin Reuptake Inhibitors-Is Pharmacogenetics the Key?

Int J Mol Sci 2016 Aug 13;17(8). Epub 2016 Aug 13.

Department of Pharmacy, Unit of PharmacoTherapy, -Epidemiology and -Economics, University of Groningen, 9713AV Groningen, The Netherlands.

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http://dx.doi.org/10.3390/ijms17081333DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5000730PMC
August 2016

When the right (Drug) should be left: Prenatal drug exposure and heterotaxy syndrome.

Birth Defects Res A Clin Mol Teratol 2016 Jul 15;106(7):573-9. Epub 2016 Mar 15.

Department of Pediatrics and Clinical Genetics, University of Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1002/bdra.23497DOI Listing
July 2016

Are congenital urinary tract and genital organ anomalies related to folic acid?

Eur Urol 2016 Mar 21;69(3):544-6. Epub 2015 Nov 21.

Eurocat Registration Northern Netherlands, Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1016/j.eururo.2015.11.006DOI Listing
March 2016

Congenital anomalies in offspring of subfertile couples: a registry-based study in the northern Netherlands.

Fertil Steril 2015 Apr 24;103(4):1001-1010.e3. Epub 2015 Jan 24.

Division of Eurocat Northern Netherlands, Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

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http://dx.doi.org/10.1016/j.fertnstert.2014.12.113DOI Listing
April 2015

Pharmacogenetics of drug-induced birth defects: the role of polymorphisms of placental transporter proteins.

Pharmacogenomics 2014 May;15(7):1029-41

Unit of Pharmacotherapy & Pharmaceutical Care, Department of Pharmacy, University of Groningen, 9713AV Groningen, The Netherlands.

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http://dx.doi.org/10.2217/pgs.14.62DOI Listing
May 2014

Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapse.

Am J Med Genet A 2014 Jan 15;164A(1):113-9. Epub 2013 Nov 15.

Department of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.36211DOI Listing
January 2014

Birth prevalence for congenital limb defects in the northern Netherlands: a 30-year population-based study.

BMC Musculoskelet Disord 2013 Nov 16;14:323. Epub 2013 Nov 16.

Department of Rehabilitation Medicine, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1186/1471-2474-14-323DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840683PMC
November 2013

A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome.

Hum Mutat 2012 Aug 11;33(8):1251-60. Epub 2012 May 11.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/humu.22106DOI Listing
August 2012

Mutation update on the CHD7 gene involved in CHARGE syndrome.

Hum Mutat 2012 Aug 16;33(8):1149-60. Epub 2012 Apr 16.

Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1002/humu.22086DOI Listing
August 2012

The results of CHD7 analysis in clinically well-characterized patients with Kallmann syndrome.

J Clin Endocrinol Metab 2012 May 7;97(5):E858-62. Epub 2012 Mar 7.

Department of Genetics, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands.

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http://dx.doi.org/10.1210/jc.2011-2652DOI Listing
May 2012

Anosmia predicts hypogonadotropic hypogonadism in CHARGE syndrome.

J Pediatr 2011 Mar;158(3):474-9

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

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http://dx.doi.org/10.1016/j.jpeds.2010.08.032DOI Listing
March 2011

CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome.

Hum Mol Genet 2010 Jul 7;19(14):2858-66. Epub 2010 May 7.

Institute of Human Genetics, University of Göttingen, 37073 Göttingen, Germany.

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http://dx.doi.org/10.1093/hmg/ddq189DOI Listing
July 2010

Study of smell and reproductive organs in a mouse model for CHARGE syndrome.

Eur J Hum Genet 2010 Feb 7;18(2):171-7. Epub 2009 Oct 7.

Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1038/ejhg.2009.158DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987182PMC
February 2010

Exon copy number alterations of the CHD7 gene are not a major cause of CHARGE and CHARGE-like syndrome.

Eur J Med Genet 2008 Sep-Oct;51(5):417-25. Epub 2008 Apr 4.

Department of Genetics, University Medical Center Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands.

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http://dx.doi.org/10.1016/j.ejmg.2008.03.003DOI Listing
November 2008

Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene.

Eur J Med Genet 2007 Sep-Oct;50(5):355-66. Epub 2007 Jul 15.

Department of Genetics, University Medical Center Groningen, University of Groningen, Post Box 30001, 9700 RB Groningen, The Netherlands.

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http://linkinghub.elsevier.com/retrieve/pii/S176972120700072
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http://dx.doi.org/10.1016/j.ejmg.2007.06.003DOI Listing
November 2007