Publications by authors named "Klaus Zerres"

100Publications

[Genetic counseling in Germany: development of demand].

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2020 Sep;63(9):1161-1167

Institut für Humangenetik, Universitätsklinikum Münster, Münster, Deutschland.

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http://dx.doi.org/10.1007/s00103-020-03206-8DOI Listing
September 2020

[Targeted Early Detection and Prevention of Hereditary Colorectal Carcinomas].

Dtsch Med Wochenschr 2020 Sep 16;145(18):1337-1346. Epub 2020 Jul 16.

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http://dx.doi.org/10.1055/a-1154-7684DOI Listing
September 2020

Serotonergic Contributions to Human Brain Aggression Networks.

Front Neurosci 2019 22;13:42. Epub 2019 Feb 22.

Department of Psychiatry, Psychotherapy and Psychosomatics, Faculty of Medicine, RWTH Aachen, Aachen, Germany.

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http://dx.doi.org/10.3389/fnins.2019.00042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395384PMC
February 2019

Neural networks underlying trait aggression depend on MAOA gene alleles.

Brain Struct Funct 2018 Mar 10;223(2):873-881. Epub 2017 Oct 10.

Department of Psychiatry, Psychotherapy, and Psychosomatics, Medical School, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany.

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http://dx.doi.org/10.1007/s00429-017-1528-6DOI Listing
March 2018

NLRP genes and their role in preeclampsia and multi-locus imprinting disorders.

J Perinat Med 2018 Feb;46(2):169-173

Institute of Human Genetics, University Hospital, Technical University (RWTH) Aachen, Aachen, Germany.

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http://dx.doi.org/10.1515/jpm-2016-0405DOI Listing
February 2018

Uniparental disomy as an unexpected cause of Meckel-Gruber syndrome: report of a case.

Pediatr Nephrol 2017 10 15;32(10):1989-1992. Epub 2017 Jun 15.

Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Pauwelsstraße 30, 52074, Aachen, Germany.

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http://dx.doi.org/10.1007/s00467-017-3710-8DOI Listing
October 2017

Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management.

J Pediatr 2017 08 19;187:206-212.e1. Epub 2017 May 19.

Institute of Human Genetics, University Hospital, Technical University Aachen (Rheinisch-Westfälische Technische Hochschule), Aachen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.jpeds.2017.04.018DOI Listing
August 2017

Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations.

Pediatr Nephrol 2017 Jul 31;32(7):1269-1273. Epub 2017 Mar 31.

Department of Pediatrics, University Hospital of Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

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http://dx.doi.org/10.1007/s00467-017-3648-xDOI Listing
July 2017

Prenatal ultrasound, genotype, and outcome in a large cohort of prenatally affected patients with autosomal-recessive polycystic kidney disease and other hereditary cystic kidney diseases.

Arch Gynecol Obstet 2017 Apr 10;295(4):897-906. Epub 2017 Mar 10.

Institute of Human Genetics, RWTH Aachen University Hospital, Pauwelsstr. 30, 52074, Aachen, Germany.

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http://link.springer.com/10.1007/s00404-017-4336-6
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http://dx.doi.org/10.1007/s00404-017-4336-6DOI Listing
April 2017

Cortico-limbic connectivity in MAOA-L carriers is vulnerable to acute tryptophan depletion.

Hum Brain Mapp 2017 03 9;38(3):1622-1635. Epub 2016 Dec 9.

Department of Psychiatry, Psychotherapy, and Psychosomatics, Medical School, RWTH Aachen University, Aachen, Germany.

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http://dx.doi.org/10.1002/hbm.23475DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6866997PMC
March 2017

Influences of Pregnancy on Different Genetic Subtypes of Non-Dystrophic Myotonia and Periodic Paralysis.

Gynecol Obstet Invest 2016 15;81(5):472-6. Epub 2016 Jun 15.

Institute of Human Genetics, Medical Faculty Uniklinik RWTH Aachen, Aachen, Germany.

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http://dx.doi.org/10.1159/000446944DOI Listing
April 2017

Distally pronounced infantile spinal muscular atrophy with severe axonal and demyelinating neuropathy associated with the S230L mutation of SMN1.

Neuromuscul Disord 2016 Feb 22;26(2):132-5. Epub 2015 Dec 22.

Institute of Human Genetics, Medical Faculty, Uniklinik RWTH Aachen, Aachen, Germany.

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http://dx.doi.org/10.1016/j.nmd.2015.12.003DOI Listing
February 2016

MAOA-VNTR polymorphism modulates context-dependent dopamine release and aggressive behavior in males.

Neuroimage 2016 Jan 16;125:378-385. Epub 2015 Oct 16.

Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, 52074 Aachen, Germany; Jülich/Aachen Research Alliance (JARA), Jülich/Aachen, Germany.

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http://dx.doi.org/10.1016/j.neuroimage.2015.10.031DOI Listing
January 2016

Clinical utility gene card for: Proximal spinal muscular atrophy (SMA) - update 2015.

Eur J Hum Genet 2015 Nov 20;23(11). Epub 2015 May 20.

Institute of Human Genetics, Medical Faculty, RWTH Aachen, Aachen, Germany.

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http://dx.doi.org/10.1038/ejhg.2015.90DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613485PMC
November 2015

Transcriptional complexity in autosomal recessive polycystic kidney disease.

Clin J Am Soc Nephrol 2014 Oct 7;9(10):1729-36. Epub 2014 Aug 7.

Center for Human Genetics, Bioscientia, Ingelheim, Germany; Department of Human Genetics, RWTH Aachen University, Aachen, Germany; and Renal Division, Department of Medicine, University Freiburg Medical Center, Freiburg, Germany

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http://dx.doi.org/10.2215/CJN.00920114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186505PMC
October 2014

Genetic variation in the G72 gene is associated with increased frontotemporal fiber tract integrity.

Eur Arch Psychiatry Clin Neurosci 2015 Jun 17;265(4):291-301. Epub 2014 Jul 17.

Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Pauwelsstrasse-30, 52074, Aachen, Germany,

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http://dx.doi.org/10.1007/s00406-014-0516-6DOI Listing
June 2015

Pontocerebellar hypoplasia.

Am J Med Genet C Semin Med Genet 2014 Jun 12;166C(2):173-83. Epub 2014 Jun 12.

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http://dx.doi.org/10.1002/ajmg.c.31403DOI Listing
June 2014

Effect of MAOA Genotype on Resting-State Networks in Healthy Participants.

Cereb Cortex 2015 Jul 22;25(7):1771-81. Epub 2014 Jan 22.

Department of Psychiatry, Psychotherapy and Psychosomatics, Medical School JARA-Translational Brain Medicine, Aachen, Germany.

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http://dx.doi.org/10.1093/cercor/bht366DOI Listing
July 2015

Neuropsychological correlates of transcription factor AP-2Beta, and its interaction with COMT and MAOA in healthy females.

Neuropsychobiology 2013 19;68(2):79-90. Epub 2013 Jul 19.

Department of Psychiatry and Psychotherapy, Medical Faculty, RWTH Aachen University, and JARA-Translational Brain Medicine, Aachen, Germany.

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http://dx.doi.org/10.1159/000350997DOI Listing
October 2014

Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies.

Arch Gynecol Obstet 2013 Nov 16;288(5):1153-8. Epub 2013 May 16.

Institute of Human Genetics, University Hospital RWTH Aachen, 52074, Aachen, Germany.

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http://dx.doi.org/10.1007/s00404-013-2861-5DOI Listing
November 2013

Multi-exon deletion in the XDH gene as a cause of classical xanthinuria.

Clin Nephrol 2013 Jan;79(1):78-80

Institute of Human Genetics, University Hospital, RWTH Aachen, Germany.

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http://dx.doi.org/10.5414/cn106994DOI Listing
January 2013

2p21 Deletions in hypotonia-cystinuria syndrome.

Eur J Med Genet 2012 Oct 17;55(10):561-3. Epub 2012 Jul 17.

Institute of Human Genetics, RWTH Aachen, Pauwelsstr. 30, D-52074 Aachen, Germany.

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http://dx.doi.org/10.1016/j.ejmg.2012.06.008DOI Listing
October 2012

Earliest ultrasound findings and description of splicing mutations in Meckel-Gruber syndrome.

Arch Gynecol Obstet 2012 Oct 15;286(4):917-21. Epub 2012 Jun 15.

Department of Gynecology and Obstetrics, University Hospital Schleswig-Holstein, Campus Kiel and Christian-Albrechts-University Kiel, Arnold-Heller-Straße 3, 24105 Kiel, Germany.

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http://link.springer.com/10.1007/s00404-012-2411-6
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http://dx.doi.org/10.1007/s00404-012-2411-6DOI Listing
October 2012

Clinical utility gene card for: proximal spinal muscular atrophy.

Eur J Hum Genet 2012 Jun 18;20(6). Epub 2012 Apr 18.

Institute of Human Genetics, Medical Faculty, RWTH Aachen, Aachen, Germany.

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http://dx.doi.org/10.1038/ejhg.2012.62DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355269PMC
June 2012

Cystinuria: an inborn cause of urolithiasis.

Orphanet J Rare Dis 2012 Apr 5;7:19. Epub 2012 Apr 5.

Institute of Human Genetics, University Hospital, RWTH Aachen, Pauwelsstr, 30, Aachen, D-52074, Germany.

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http://ojrd.biomedcentral.com/articles/10.1186/1750-1172-7-1
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http://dx.doi.org/10.1186/1750-1172-7-19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464901PMC
April 2012

Pregnancy course and outcome in women with hereditary neuromuscular disorders: comparison of obstetric risks in 178 patients.

Eur J Obstet Gynecol Reprod Biol 2012 Jun 28;162(2):153-9. Epub 2012 Mar 28.

Institute of Human Genetics, Medical Faculty, RWTH Aachen, Germany.

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http://dx.doi.org/10.1016/j.ejogrb.2012.02.020DOI Listing
June 2012

SETX gene mutation in a family diagnosed autosomal dominant proximal spinal muscular atrophy.

Neuromuscul Disord 2012 Mar 15;22(3):258-62. Epub 2011 Nov 15.

Institute of Human Genetics, Medical Faculty, RWTH Aachen, Germany.

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http://dx.doi.org/10.1016/j.nmd.2011.09.006DOI Listing
March 2012

Mutations in TRPV4 cause an inherited arthropathy of hands and feet.

Nat Genet 2011 Oct 2;43(11):1142-6. Epub 2011 Oct 2.

Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia.

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http://dx.doi.org/10.1038/ng.945DOI Listing
October 2011

Recurrence risks of hypertensive diseases in pregnancy after HELLP syndrome.

J Perinat Med 2011 11 2;39(6):673-8. Epub 2011 Aug 2.

Department of Obstetrics and Gynecology, Aachen University (RWTH), Aachen, Germany.

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https://www.degruyter.com/view/j/jpme.2011.39.issue-6/jpm.20
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http://dx.doi.org/10.1515/jpm.2011.081DOI Listing
November 2011

Cerebral folate deficiency: a neurometabolic syndrome?

Mol Genet Metab 2011 Nov 14;104(3):369-72. Epub 2011 Jun 14.

Department of Pediatrics, University Hospital RWTH Aachen, Germany.

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http://dx.doi.org/10.1016/j.ymgme.2011.06.004DOI Listing
November 2011

Megalencephaly, mega corpus callosum, and complete lack of motor development: delineation of a rare syndrome.

Am J Med Genet A 2010 Sep;152A(9):2360-4

Department of Pediatrics, University Hospital, RWTH Aachen, Aachen, Germany.

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http://dx.doi.org/10.1002/ajmg.a.33577DOI Listing
September 2010

Digital necroses and vascular thrombosis in severe spinal muscular atrophy.

Muscle Nerve 2010 Jul;42(1):144-7

Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Pauwelsstrasse 30, D-52074 Aachen, Germany.

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http://dx.doi.org/10.1002/mus.21654DOI Listing
July 2010

Facioaudiosymphalangism syndrome and growth acceleration associated with a heterozygous NOG mutation.

Am J Med Genet A 2010 Jun;152A(6):1540-4

Medical Faculty, Institute of Human Genetics, RWTH Aachen University, Aachen, Germany.

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http://dx.doi.org/10.1002/ajmg.a.33387DOI Listing
June 2010

The mTOR pathway is activated in human autosomal-recessive polycystic kidney disease.

Kidney Blood Press Res 2010 12;33(2):129-38. Epub 2010 May 12.

Institute of Pathology and Neuropathology, University Hospital of Essen, University Duisburg-Essen, Essen, Germany.

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http://dx.doi.org/10.1159/000314380DOI Listing
September 2010

Genetic loci influencing kidney function and chronic kidney disease.

Authors:
John C Chambers Weihua Zhang Graham M Lord Pim van der Harst Debbie A Lawlor Joban S Sehmi Daniel P Gale Mark N Wass Kourosh R Ahmadi Stephan J L Bakker Jacqui Beckmann Henk J G Bilo Murielle Bochud Morris J Brown Mark J Caulfield John M C Connell H Terence Cook Ioana Cotlarciuc George Davey Smith Ranil de Silva Guohong Deng Olivier Devuyst Lambert D Dikkeschei Nada Dimkovic Mark Dockrell Anna Dominiczak Shah Ebrahim Thomas Eggermann Martin Farrall Luigi Ferrucci Jurgen Floege Nita G Forouhi Ron T Gansevoort Xijin Han Bo Hedblad Jaap J Homan van der Heide Bouke G Hepkema Maria Hernandez-Fuentes Elina Hypponen Toby Johnson Paul E de Jong Nanne Kleefstra Vasiliki Lagou Marta Lapsley Yun Li Ruth J F Loos Jian'an Luan Karin Luttropp Céline Maréchal Olle Melander Patricia B Munroe Louise Nordfors Afshin Parsa Leena Peltonen Brenda W Penninx Esperanza Perucha Anneli Pouta Inga Prokopenko Paul J Roderick Aimo Ruokonen Nilesh J Samani Serena Sanna Martin Schalling David Schlessinger Georg Schlieper Marc A J Seelen Alan R Shuldiner Marketa Sjögren Johannes H Smit Harold Snieder Nicole Soranzo Timothy D Spector Peter Stenvinkel Michael J E Sternberg Ramasamyiyer Swaminathan Toshiko Tanaka Lielith J Ubink-Veltmaat Manuela Uda Peter Vollenweider Chris Wallace Dawn Waterworth Klaus Zerres Gerard Waeber Nicholas J Wareham Patrick H Maxwell Mark I McCarthy Marjo-Riitta Jarvelin Vincent Mooser Goncalo R Abecasis Liz Lightstone James Scott Gerjan Navis Paul Elliott Jaspal S Kooner

Nat Genet 2010 May 11;42(5):373-5. Epub 2010 Apr 11.

Department of Epidemiology and Biostatistics, School of Public Health, Imperial College of London, London, UK.

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http://dx.doi.org/10.1038/ng.566DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748585PMC
May 2010

COMT genotype and its role on hippocampal-prefrontal regions in declarative memory.

Neuroimage 2010 Nov 11;53(3):978-84. Epub 2010 Jan 11.

Department of Psychiatry and Psychotherapy, Section of Brain Imaging, Philipps-University Marburg, Rudolf-Bultmann-Str. 8, 35039 Marburg, Germany.

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http://dx.doi.org/10.1016/j.neuroimage.2009.12.090DOI Listing
November 2010

The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval.

Neuroimage 2010 Nov 28;53(3):985-91. Epub 2009 Dec 28.

Department of Psychiatry and Psychotherapy, Philipps-University Marburg, Rudolf-Bultmann-Str. 8, 35039 Marburg, Germany.

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http://dx.doi.org/10.1016/j.neuroimage.2009.12.062DOI Listing
November 2010

The effect of G72 genotype on neural correlates of memory encoding and retrieval.

Neuroimage 2010 Nov 11;53(3):1001-6. Epub 2009 Dec 11.

Section of BrainImaging, Department of Psychiatry and Psychotherapy, Philipps-University Marburg, Germany.

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http://dx.doi.org/10.1016/j.neuroimage.2009.12.018DOI Listing
November 2010

Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype.

Am J Med Genet A 2009 Nov;149A(11):2547-50

Medical Faculty, Institute of Human Genetics, University Hospital, RWTH Aachen University, Aachen, Germany.

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http://dx.doi.org/10.1002/ajmg.a.33086DOI Listing
November 2009

Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals.

Neuroimage 2010 Jan 23;49(2):1831-6. Epub 2009 Sep 23.

Department of Psychiatry, Philipps-University Marburg, Rudolf-Bultmann-Str. 8, 35039 Marburg, Germany.

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http://dx.doi.org/10.1016/j.neuroimage.2009.09.028DOI Listing
January 2010

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects.

BMC Psychiatry 2009 Sep 24;9:60. Epub 2009 Sep 24.

Section of BrainImaging, Department of Psychiatry and Psychotherapy, Philipps-University Marburg, Germany.

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http://dx.doi.org/10.1186/1471-244X-9-60DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761379PMC
September 2009

Parathyroid hormone gene variant and calcific aortic stenosis.

J Heart Valve Dis 2009 May;18(3):262-7

Division of Cardiology, Pulmonary Diseases, and Vascular Medicine, Department of Medicine, University Hospital RWTH Aachen, Germany.

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May 2009

The effect of the COMT val(158)met polymorphism on neural correlates of semantic verbal fluency.

Eur Arch Psychiatry Clin Neurosci 2009 Dec 21;259(8):459-65. Epub 2009 Apr 21.

Department of Psychiatry and Psychotherapy, Philipps-University Marburg, Rudolf-Bultmann-Str. 8, 35039, Marburg, Germany.

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http://dx.doi.org/10.1007/s00406-009-0010-8DOI Listing
December 2009

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.

Cancer Res 2009 Apr 7;69(8):3650-6. Epub 2009 Apr 7.

Department of Nephrology, Section of Preventive Medicine, Albert-Ludwigs University, Freiburg, Germany.

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http://cancerres.aacrjournals.org/content/early/2009/04/07/0
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http://cancerres.aacrjournals.org/cgi/doi/10.1158/0008-5472.
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http://dx.doi.org/10.1158/0008-5472.CAN-08-4057DOI Listing
April 2009

Interleukin-1 polymorphisms in relation to external apical root resorption (EARR).

J Orofac Orthop 2009 Jan 5;70(1):20-38. Epub 2009 Feb 5.

Department of Orthodontics, RWTH Aachen University, Aachen, Germany.

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http://dx.doi.org/10.1007/s00056-009-8808-6DOI Listing
January 2009

Identification of novel cystinuria mutations in pediatric patients.

J Pediatr Urol 2006 Dec 19;2(6):575-8. Epub 2006 Jan 19.

Institute of Human Genetics, University Hospital, RWTH, Pauwelsstr. 30, D-52074 Aachen, Germany.

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http://dx.doi.org/10.1016/j.jpurol.2005.11.011DOI Listing
December 2006

No evidence for a role of cosmc-chaperone mutations in European IgA nephropathy patients.

Nephrol Dial Transplant 2009 Jan 7;24(1):321-4. Epub 2008 Oct 7.

Department of Human Genetics, Division of Nephrology and Immunology, Aachen, Germany.

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http://dx.doi.org/10.1093/ndt/gfn538DOI Listing
January 2009

Genetic analysis of the angiotensinogen gene in pre-eclampsia: study of german women and review of the literature.

Gynecol Obstet Invest 2008 22;66(3):203-8. Epub 2008 Jul 22.

Institute of Human Genetics, University Hospital of Aachen, Aachen, Germany.

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http://dx.doi.org/10.1159/000146084DOI Listing
January 2009

A new case of proximal monosomy 1p36, extending the phenotype.

Am J Med Genet A 2008 Aug;146A(15):2018-22

Institute of Human Genetics, University Hospital RWTH Aachen, Aachen, Germany.

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http://dx.doi.org/10.1002/ajmg.a.32405DOI Listing
August 2008

Maternal factor V Leiden mutation is associated with HELLP syndrome in Caucasian women.

Acta Obstet Gynecol Scand 2008 ;87(6):635-42

Department of Obstetrics and Gynecology, RWTH Aachen University Hospital, Aachen, Germany.

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http://dx.doi.org/10.1080/00016340802112740DOI Listing
July 2008

Nephrectomy in an autosomal recessive polycystic kidney disease (ARPKD) patient with rapid kidney enlargement and increased expression of EGFR.

Nephrol Dial Transplant 2008 Sep 23;23(9):3026-9. Epub 2008 May 23.

Department of Pediatrics II, University of Duisburg-Essen, Hufelandstr. 55, 45122 Essen, Germany.

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http://dx.doi.org/10.1093/ndt/gfn288DOI Listing
September 2008

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with personality traits in healthy individuals.

Eur Psychiatry 2008 Aug 1;23(5):344-9. Epub 2008 May 1.

Department of Psychiatry and Psychotherapy, RWTH Aachen University, Pauwelsstrasse 30, D-52074 Aachen, Germany.

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http://dx.doi.org/10.1016/j.eurpsy.2008.03.004DOI Listing
August 2008

Spinal muscular atrophy with respiratory distress type 1 (SMARD1).

J Child Neurol 2008 Feb;23(2):199-204

Department of Pediatric Neurology, Charité, University Medical Center, Berlin, Germany.

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http://dx.doi.org/10.1177/0883073807310989DOI Listing
February 2008

Genes and the preeclampsia syndrome.

J Perinat Med 2008 ;36(1):38-58

Department of Obstetrics and Gynecology, Aachen University (RWTH), Aachen, Germany.

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http://dx.doi.org/10.1515/JPM.2008.004DOI Listing
May 2008

A new splice site mutation in the SMN1 gene causes discrepant results in SMN1 deletion screening approaches.

Neuromuscul Disord 2008 Feb 21;18(2):146-9. Epub 2007 Dec 21.

Institute of Human Genetics, Technical University of Aachen, Pauwelsstr. 30, D-52074 Aachen, Germany.

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http://dx.doi.org/10.1016/j.nmd.2007.10.003DOI Listing
February 2008

The 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene is not associated with HELLP syndrome.

J Thromb Thrombolysis 2009 Feb 6;27(2):141-5. Epub 2007 Dec 6.

Department of Obstetrics and Gynecology, Aachen University (RWTH), Aachen, Germany.

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http://dx.doi.org/10.1007/s11239-007-0175-9DOI Listing
February 2009

Early manifestations of polycystic kidney disease.

Lancet 2007 Jun;369(9580):2157

Department of Human Genetics, RWTH Aachen University, Pauwelsstrasse 30, D-52074 Aachen, Germany.

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http://dx.doi.org/10.1016/S0140-6736(07)61005-8DOI Listing
June 2007