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1

Maternal uniparental disomy 14 in a 15-year-old boy with normal karyotype and no evidence of precocious puberty

Stefan Aretz, Ruth Raff, Joachim Woelfle, Klaus Zerres, Marianne Esser, Peter Propping, Thomas Eggermann

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 83 KB

english, 2005

2

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology

Zerres, Klaus, M�cher, Gabi, Becker, Jutta, Steinkamm, Carsten, Rudnik-Sch�neborn, Sabine, Heikkil�, P�ivi, Rapola, Juhani, Salonen, Riitta, Germino, Gregory G., Onuchic, Luiz, Somlo, Stefan, Avner, E

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 339 KB

english, 1998

3

Algorithm for efficient PKHD1 mutation screening in autosomal recessive polycystic kidney disease (ARPKD)

Carsten Bergmann, Fabian Küpper, Christian Dornia, Frank Schneider, Jan Senderek, Klaus Zerres

Journal:

Year:

2005

Language:

english

File:

PDF, 392 KB

english, 2005

4

Mutation analysis of the growth factor genes PlGF, Flt1, IGF-I , and IGF-IR in intrauterine growth restriction with abnormal placental blood flow

Muetze, Sabine, Kapagerof, Athina, Vlachopoulos, Lazaros, Eggermann, Thomas, Kaufmann, Peter, Zerres, Klaus, Rath, Werner, Rudnik-Schoeneborn, Sabine

Journal:

Journal of Maternal-Fetal and Neonatal Medicine

Year:

2010

Language:

english

File:

PDF, 305 KB

english, 2010

5

Does it take two to tango? Longitudinal effects of unilateral and bilateral integrative negotiation training.

Zerres, Alfred, Hüffmeier, Joachim, Freund, Philipp Alexander, Backhaus, Klaus, Hertel, Guido

Journal:

Journal of Applied Psychology

Year:

2013

Language:

english

File:

PDF, 257 KB

english, 2013

6

Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC)

Carsten Bergmann, Klaus Zerres, Thomas Peschgens, Jan Senderek, Helmut Hörnchen, Sabine Rudnik-Schöneborn

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 172 KB

english, 2003

7

PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)

Carsten Bergmann, Jan Senderek, Frank Schneider, Christian Dornia, Fabian Küpper, Thomas Eggermann, Sabine Rudnik-Schöneborn, Jutta Kirfel, Markus Moser, Reinhard Büttner, Klaus Zerres

Journal:

Year:

2004

Language:

english

File:

PDF, 163 KB

english, 2004

8

Digital necroses and vascular thrombosis in severe spinal muscular atrophy

Sabine Rudnik-Schöneborn, Silke Vogelgesang, Sven Armbrust, Luitgard Graul-Neumann, Christoph Fusch, Klaus Zerres

Journal:

Year:

2010

Language:

english

File:

PDF, 191 KB

english, 2010

9

Cerebral folate deficiency: A neurometabolic syndrome?

Sarah Mangold, Nenad Blau, Thomas Opladen, Robert Steinfeld, Britta Weßling, Klaus Zerres, Martin Häusler

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 236 KB

english, 2011

10

Cystinuria: an inborn cause of urolithiasis

Thomas Eggermann, Andreas Venghaus, Klaus Zerres

Journal:

Orphanet Journal of Rare Diseases

Year:

2012

Language:

english

File:

PDF, 381 KB

english, 2012

11

Präimplantationsdiagnostik im Europavergleich

Sandra Geffroy,Prof. Dr. med. Klaus Zerres

Journal:

medizinische genetik

Year:

2016

Language:

german

File:

PDF, 203 KB

german, 2016

12

Strong or Weak Synergy? Revising the Assumption of Team-Related Advantages in Integrative Negotiations

Hüffmeier, Joachim, Zerres, Alfred, Freund, Philipp Alexander, Backhaus, Klaus, Trötschel, Roman, Hertel, Guido

Journal:

Journal of Management

Year:

2018

Language:

english

File:

PDF, 161 KB

english, 2018

13

Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus

Rudnik-Sch�neborn, Sabine, Nicholson, Garth A., Morgan, Graeme, R�hrig, Dorothee, Zerres, Klaus

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 113 KB

english, 1998

14

Adult syndrome allelic to limb mammary syndrome (LMS)?

Propping, Peter, Friedl, Waltraut, Wienker, Thomas F., Uhlhaas, Siegfried, Zerres, Klaus

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 125 KB

english, 2000

15

Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene

Luiz F. Onuchic, Michal Mrug, Xiaoying Hou, Thomas Eggermann, Carsten Bergmann, Klaus Zerres, Ellis D. Avner, Laszlo Furu, Stefan Somlo, Yasuyuki Nagasawa, Gregory G. Germino, Lisa M. Guay-Woodford

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 182 KB

english, 2002

16

ADULT-syndrome: An autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia

Prof., Dr. Peter Propping, Klaus Zerres

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 2.53 MB

english, 1993

17

Steinfeld syndrome: Report of a second family and further delineation of a rare autosomal dominant disorder

Dr. Markus M. Nöthen, Gisela Knöpfle, Hans-Jörg Födisch, Klaus Zerres

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 397 KB

english, 1993

18

Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: Clinical picture, influence of gender, and genetic implications

Sabine Rudnik-Schöneborn, Dorothee Röhrig, Graeme Morgan, Brunhilde Wirth, Klaus Zerres

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 751 KB

english, 1994

19

Extended phenotype of pontocerebellar hypoplasia with infantile spinal muscular atrophy

Sabine Rudnik-Schöneborn, László Sztriha, Gururaj R. Aithala, Gunnar Houge, Liv M. Lægreid, Jürgen Seeger, Michael Huppke, Brunhilde Wirth, Klaus Zerres

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 282 KB

english, 2003

20

Clinical and genetic heterogeneity in Desbuquois dysplasia

Laurence Faivre, Martine Le Merrer, Klaus Zerres, Mongi Ben Hariz, Déborah Scheffer, Ian D. Young, Pierre Maroteaux, Arnold Munnich, Valérie Cormier-Daire

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 175 KB

english, 2004

21

Rare proximal interstitial deletion of chromosome 4q, del(4)(q13.2q21.22): New case and comparison with the literature

Katja Eggermann, Carsten Bergmann, Inge Heil, Thomas Eggermann, Klaus Zerres, Herdit M. Schüler

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 83 KB

english, 2005

22

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

Sabine Rudnik-Schöneborn, Klaus Zerres, Martin Häusler, Alexandra Lott, Timo Krings, Herdit M. Schüler

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 183 KB

english, 2008

23

Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees

Hartmut Engels, Thomas Eggermann, Almut Caliebe, Anna Jelska, Regine Schubert, Herdit M. Schüler, Barbara Panasiuk, Jacek Zaremba, Anna Latos-Bieleńska, Lucjusz Jakubowski, Klaus P. Zerres, Gesa Schwa

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 78 KB

english, 2008

24

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

Miriam Elbracht, Andreas Roos, Nadine Schönherr, Sabine Busse, Reinhild Damen, Klaus Zerres, Sabine Rudnik-Schöneborn, Herdit Monika Schüler

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 126 KB

english, 2009

25

Facioaudiosymphalangism syndrome and growth acceleration associated with a heterozygous NOG mutation

Sabine Rudnik-Schöneborn, Tsutomu Takahashi, Sabine Busse, Thorsten Schmidt, Jan Senderek, Thomas Eggermann, Klaus Zerres

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 203 KB

english, 2010

26

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

Meike Hengst, Jens Tücke, Klaus Zerres, Marcus Blaum, Martin Häusler

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 126 KB

english, 2010

27

Consequences of a novel caveolin-3 mutation in a large German family

Dirk Fischer, Anja Schroers, Ingmar Blümcke, Horst Urbach, Klaus Zerres, Wilhelm Mortier, Matthias Vorgerd, Rolf Schröder

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 736 KB

english, 2003

28

Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals

Tilo Kircher, Axel Krug, Valentin Markov, Carin Whitney, Sören Krach, Klaus Zerres, Thomas Eggermann, Tony Stöcker, Nadim Jon Shah, Jens Treutlein, Markus M. Nöthen, Tim Becker, Marcella Rietschel

Journal:

Human Brain Mapping

Year:

2009

Language:

english

File:

PDF, 257 KB

english, 2009

29

The impact of dystrobrevin-binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval

Markus Thimm, Axel Krug, Valentin Markov, Sören Krach, Andreas Jansen, Klaus Zerres, Thomas Eggermann, Tony Stöcker, Nadim Jon Shah, Markus M. Nöthen, Marcella Rietschel, Tilo Kircher

Journal:

Human Brain Mapping

Year:

2010

Language:

english

File:

PDF, 148 KB

english, 2010

30

Genetic variation in G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals

Axel Krug, Valentin Markov, Sören Krach, Andreas Jansen, Klaus Zerres, Thomas Eggermann, Tony Stöcker, N Jon Shah, Markus M Nöthen, Alexander Georgi, Jana Strohmaier, Marcella Rietschel, Tilo Kircher

Journal:

Human Brain Mapping

Year:

2011

Language:

english

File:

PDF, 154 KB

english, 2011

31

A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)

Markus Moser, Sonja Matthiesen, Jutta Kirfel, Hubert Schorle, Carsten Bergmann, Jan Senderek, Sabine Rudnik-Schöneborn, Klaus Zerres, Reinhard Buettner

Journal:

Year:

2005

Language:

english

File:

PDF, 1.98 MB

english, 2005

32

Determination of SMN1 and SMN2 copy number using TaqMan™ technology

Dirk Anhuf, Thomas Eggermann, Sabine Rudnik-Schöneborn, Klaus Zerres

Journal:

Year:

2003

Language:

english

File:

PDF, 112 KB

english, 2003

33

Phenotype Diversity in Familial Cylindromatosis: A Frameshift Mutation in the Tumor Suppressor Gene CYLD Underlies Different Tumors of Skin Appendages

Gutierrez, Pamela Poblete, Eggermann, Thomas, Holler, Daniela, Jugert, Frank K., Beermann, Torsten, Grussendorf-Conen, Elke-Ingrid, Zerres, Klaus, Merk, Hans F., Frank, Jorge

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 273 KB

english, 2002

34

Significant contribution of genomic rearrangements in SLC3A1 and SLC7A9 to the etiology of cystinuria

Schmidt, Christa, Vester, Udo, Wagner, Carsten A., Lahme, Sven, Hesse, Albrecht, Hoyer, Peter, Lang, Florian, Zerres, Klaus, Eggermann, Thomas

Journal:

Kidney International

Year:

2003

Language:

english

File:

PDF, 1.08 MB

english, 2003

35

Immunochemical determination of cellular prion proteinin plasma from healthy subjects and patients withsporadic CJD or other neurologic diseases

Dirk Völkel, Klaus Zimmermann, Inga Zerr, Monica Bodemer, Thomas Lindner, Peter L. Turecek, Sigrid Poser, Hans P. Schwarz

Journal:

Transfusion (Wiley)

Year:

2001

Language:

english

File:

PDF, 120 KB

english, 2001

36

Reply

Dirk Völkel, Klaus Zimmermann, Inga Zerr, Monica Bodemer, Thomas Linder, Peter L. Turecek, Sigrid Poser, Hans Peter Schwarz

Journal:

Transfusion (Wiley)

Year:

2001

Language:

english

File:

PDF, 32 KB

english, 2001

37

C-reactive protein and IL-6: new marker proteins for the diagnosis of CJD in plasma?

Dirk Völkel, Klaus Zimmermann, Inga Zerr, Thomas Lindner, Monica Bodemer, Sigrid Poser, Hans Peter Schwarz

Journal:

Transfusion (Wiley)

Year:

2001

Language:

english

File:

PDF, 104 KB

english, 2001

38

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait

Francesco P Schena, Giuseppina Cerullo, Diletta D Torres, Francesco Scolari, Marina Foramitti, Antonio Amoroso, Doroti Pirulli, Jürgen Floege, Peter R Mertens, Klaus Zerres, Efstathios Alexopoulos, Di

Journal:

Year:

2005

Language:

english

File:

PDF, 874 KB

english, 2005

39

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

Andreas Jansen, Sören Krach, Axel Krug, Valentin Markov, Thomas Eggermann, Klaus Zerres, Markus Thimm, Markus M Nöthen, Jens Treutlein, Marcella Rietschel, Tilo Kircher

Journal:

Year:

2009

Language:

english

File:

PDF, 853 KB

english, 2009

40

Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4

Klaus Zerres, Gabi Mücher, Sabine Rudnik-Schöneborn

Journal:

Year:

1994

Language:

english

File:

PDF, 166 KB

english, 1994

41

No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers

Katrin Kausch, Clemens R. Müller, Tiemo Grimm, Kenneth Ricker, Marcella Rietschel, Sabine Rudnik-Schöneborn, Klaus Zerres

Journal:

Year:

1991

Language:

english

File:

PDF, 127 KB

english, 1991

42

Pregnancy and spinal muscular atrophy

Sabine Rudnik-Schöneborn, Klaus Zerres, Jaakko Ignatius, Marcella Rietschel

Journal:

Journal of Neurology

Year:

1992

Language:

english

File:

PDF, 471 KB

english, 1992

43

Genetics of cystic kidney diseases

Journal:

Pediatric Nephrology

Year:

1987

Language:

english

File:

PDF, 1.21 MB

english, 1987

44

Interleukin-1 Polymorphisms in Relation to External Apical Root Resorption (EARR)

Norbert Gülden, Thomas Eggermann, Klaus Zerres, Michael Beer, Anica Meinelt, Peter Diedrich

Journal:

Journal of Orofacial Orthopedics/Fortschritte der Kieferorthopädie

Year:

2009

File:

PDF, 876 KB

2009

45

Chemokine receptor (CCR2) genotype is associated with myocardial infarction and heart failure in patients under 65

Jan R. Ortlepp, Katharina Vesper, Vera Mevissen, Fabian Schmitz, Uwe Janssens, Andreas Franke, Peter Hanrath, Christian Weber, Klaus Zerres, Rainer Hoffmann

Journal:

Journal of Molecular Medicine

Year:

2003

Language:

english

File:

PDF, 165 KB

english, 2003

46

Obesity is associated with a slower response to initial phenprocoumon therapy whereas CYP2C9 genotypes are not

Cordula Meyer zu Schwabedissen, Vera Mevissen, Fabian Schmitz, Seth Woodruff, Georg Langebartels, Thomas Rau, Klaus Zerres, Rainer Hoffmann, Jan R. Ortlepp

Journal:

European Journal of Clinical Pharmacology

Year:

2006

Language:

english

File:

PDF, 162 KB

english, 2006

47

The population-specific distribution and frequencies of genomic variants in theSLC3A1andSLC7A9genes and their application in molecular genetic testing of cystinuria

Christa Schmidt, Udo Vester, Albrecht Hesse, Sven Lahme, Florian Lang, Klaus Zerres, Thomas Eggermann, members of the Arbeitsgemeinschaft Pädiatrische Nephrologie

Journal:

Year:

2004

Language:

english

File:

PDF, 159 KB

english, 2004

48

Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate gene

Luiz F. Onuchic, Michal Mrug, Alicia L. Lakings, Gabi Muecher, Jutta Becker, Klaus Zerres, Ellis D. Avner, Mehul Dixit, Stefan Somlo, Gregory G. Germino, Lisa M. Guay-Woodford

Journal:

Mammalian Genome

Year:

1999

Language:

english

File:

PDF, 237 KB

english, 1999

49

The effect of the COMT val158met polymorphism on neural correlates of semantic verbal fluency

Axel Krug, Valentin Markov, Abigail Sheldrick, Sören Krach, Andreas Jansen, Klaus Zerres, Thomas Eggermann, Tony Stöcker, N. Jon Shah, Tilo Kircher

Journal:

European Archives of Psychiatry and Clinical Neuroscience

Year:

2009

Language:

english

File:

PDF, 225 KB

english, 2009

50

Positron emission tomography with [18F]FDG in the diagnosis of Creutzfeldt-Jakob disease (CJD)

Karsten Henkel, Inga Zerr, Andreas Hertel, Klaus-F. Gratz, Andreas Schröter, Henriette J. Tschampa, Heiner Bihl, Udalrich Büll, Frank Grünwald, Alexander Drzezga, Jörg Spitz, Sigrid Poser

Journal:

Journal of Neurology

Year:

2002

Language:

english

File:

PDF, 243 KB

english, 2002