Publications by authors named "Kerstin U Ludwig"

61Publications

Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms.

Genet Epidemiol 2020 Jul 24. Epub 2020 Jul 24.

Medical Research Council Integrative Epidemiology Unit, Population Health Sciences, University of Bristol, Bristol, UK.

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http://dx.doi.org/10.1002/gepi.22343DOI Listing
July 2020

deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development.

Development 2020 Jun 24;147(21). Epub 2020 Jun 24.

Biosciences Institute, Newcastle University, International Centre for Life, Newcastle upon Tyne NE1 3BZ, UK

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http://dx.doi.org/10.1242/dev.189175DOI Listing
June 2020

p63 establishes epithelial enhancers at critical craniofacial development genes.

Sci Adv 2019 05 1;5(5):eaaw0946. Epub 2019 May 1.

Departments of Cell and Developmental Biology and Epigenetics Institute, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.1126/sciadv.aaw0946DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494499PMC
May 2019

Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety.

Psychiatr Genet 2017 06;27(3):96-102

aInstitute of Human Genetics bDepartment of Genomics, Life and Brain Center cClinic for Psychosomatic Medicine and Psychotherapy, University of Bonn, Bonn dDepartment of Psychotherapy and Psychosomatic Medicine, University Hospital Carl Gustav Carus, Technische Universitaet Dresden, Dresden, Germany eDepartment of Psychiatry (UPK) fHuman Genomics Research Group, Department of Biomedicine, University of Basel gInstitute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.

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http://dx.doi.org/10.1097/YPG.0000000000000171DOI Listing
June 2017

Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.

Nat Commun 2017 02 24;8:14364. Epub 2017 Feb 24.

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) and Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan, Hubei 430079, China.

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http://dx.doi.org/10.1038/ncomms14364DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333091PMC
February 2017

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.

Psychiatr Genet 2016 12;26(6):293-296

aInstitute of Human Genetics bDepartment of Genomics, Life and Brain Center cDepartment of Psychiatry and Psychotherapy dDepartment of Clinical Chemistry and Clinical Pharmacology, University of Bonn, Bonn eDepartment of Psychiatry, Ludwig-Maximilians-University Munich fKbo Kliniken des Bezirks Oberbayern, Munich gDepartment of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Heidelberg hDepartment of Psychiatry, University of Halle-Wittenberg, Halle iIsar Amper Klinikum München Ost, kbo, Haar jInstitute of Neuroscience and Medicine (INM-1), Structural and Functional Organisation of the Brain, Genomic Imaging, Research Centre Juelich, Juelich, Germany kFaculty of Science, Medicine & Health, University of Wollongong, Wollongong, Australia lDepartment of Biomedicine, Division of Medical Genetics, University Hospital Basel, University of Basel, Basel, Switzerland.

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http://dx.doi.org/10.1097/YPG.0000000000000145DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087564PMC
December 2016

A post GWAS association study of SNPs associated with cleft lip with or without cleft palate in submucous cleft palate.

Am J Med Genet A 2015 Mar;167A(3):670-3

Section of Phoniatrics and Pedaudiology, Department of Otolaryngology - Head and Neck Surgery, University of Ulm, Ulm, Germany.

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http://dx.doi.org/10.1002/ajmg.a.36891DOI Listing
March 2015

Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.

Birth Defects Res A Clin Mol Teratol 2014 Jun 7;100(6):493-8. Epub 2014 Apr 7.

Institute of Human Genetics, University of Bonn, Bonn, Germany; Klinikverbund St. Antonius und St. Josef, Wuppertal, Germany; Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany.

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http://dx.doi.org/10.1002/bdra.23244DOI Listing
June 2014

Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.

Birth Defects Res A Clin Mol Teratol 2014 Jan 31;100(1):43-7. Epub 2013 Dec 31.

Institute of Human Genetics, University of Bonn, Bonn, Germany; Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany.

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http://dx.doi.org/10.1002/bdra.23209DOI Listing
January 2014

Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.

Eur J Hum Genet 2014 Jun 30;22(6):822-30. Epub 2013 Oct 30.

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, Hess Center for Science and Medicine, New York, NY, USA.

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http://dx.doi.org/10.1038/ejhg.2013.235DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023210PMC
June 2014

Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample.

Am J Med Genet A 2013 Oct 16;161A(10):2545-9. Epub 2013 Aug 16.

Institute of Human Genetics, University of Bonn, Bonn, Germany; Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany.

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http://dx.doi.org/10.1002/ajmg.a.36141DOI Listing
October 2013

Breakthroughs in the genetics of orofacial clefting.

Trends Mol Med 2011 Dec 30;17(12):725-33. Epub 2011 Aug 30.

Institute of Human Genetics, University of Bonn, Sigmund-Freud-Str. 25, 53127 Bonn, Germany.

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http://dx.doi.org/10.1016/j.molmed.2011.07.007DOI Listing
December 2011

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.

J Neural Transm (Vienna) 2008 Nov 23;115(11):1587-9. Epub 2008 Sep 23.

Department of Genomics, Life and Brain Center, University of Bonn, Sigmund-Freud Str. 25, 53105, Bonn, Germany.

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http://link.springer.com/10.1007/s00702-008-0124-6
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http://dx.doi.org/10.1007/s00702-008-0124-6DOI Listing
November 2008