Walter Just

Walter Just

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Walter Just

Walter Just

Publications by authors named "Walter Just"

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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

Authors:
Yosr Hamdi Penny Soucy Karoline B Kuchenbaeker Tomi Pastinen Arnaud Droit Audrey Lemaçon Julian Adlard Kristiina Aittomäki Irene L Andrulis Adalgeir Arason Norbert Arnold Banu K Arun Jacopo Azzollini Anita Bane Laure Barjhoux Daniel Barrowdale Javier Benitez Pascaline Berthet Marinus J Blok Kristie Bobolis Valérie Bonadona Bernardo Bonanni Angela R Bradbury Carole Brewer Bruno Buecher Saundra S Buys Maria A Caligo Jocelyne Chiquette Wendy K Chung Kathleen B M Claes Mary B Daly Francesca Damiola Rosemarie Davidson Miguel De la Hoya Kim De Leeneer Orland Diez Yuan Chun Ding Riccardo Dolcetti Susan M Domchek Cecilia M Dorfling Diana Eccles Ros Eeles Zakaria Einbeigi Bent Ejlertsen Christoph Engel D Gareth Evans Lidia Feliubadalo Lenka Foretova Florentia Fostira William D Foulkes George Fountzilas Eitan Friedman Debra Frost Pamela Ganschow Patricia A Ganz Judy Garber Simon A Gayther Anne-Marie Gerdes Gord Glendon Andrew K Godwin David E Goldgar Mark H Greene Jacek Gronwald Eric Hahnen Ute Hamann Thomas V O Hansen Steven Hart John L Hays Frans B L Hogervorst Peter J Hulick Evgeny N Imyanitov Claudine Isaacs Louise Izatt Anna Jakubowska Paul James Ramunas Janavicius Uffe Birk Jensen Esther M John Vijai Joseph Walter Just Katarzyna Kaczmarek Beth Y Karlan Carolien M Kets Judy Kirk Mieke Kriege Yael Laitman Maïté Laurent Conxi Lazaro Goska Leslie Jenny Lester Fabienne Lesueur Annelie Liljegren Niklas Loman Jennifer T Loud Siranoush Manoukian Milena Mariani Sylvie Mazoyer Lesley McGuffog Hanne E J Meijers-Heijboer Alfons Meindl Austin Miller Marco Montagna Anna Marie Mulligan Katherine L Nathanson Susan L Neuhausen Heli Nevanlinna Robert L Nussbaum Edith Olah Olufunmilayo I Olopade Kai-Ren Ong Jan C Oosterwijk Ana Osorio Laura Papi Sue Kyung Park Inge Sokilde Pedersen Bernard Peissel Pedro Perez Segura Paolo Peterlongo Catherine M Phelan Paolo Radice Johanna Rantala Christine Rappaport-Fuerhauser Gad Rennert Andrea Richardson Mark Robson Gustavo C Rodriguez Matti A Rookus Rita Katharina Schmutzler Nicolas Sevenet Payal D Shah Christian F Singer Thomas P Slavin Katie Snape Johanna Sokolowska Ida Marie Heeholm Sønderstrup Melissa Southey Amanda B Spurdle Zsofia Stadler Dominique Stoppa-Lyonnet Grzegorz Sukiennicki Christian Sutter Yen Tan Muy-Kheng Tea Manuel R Teixeira Alex Teulé Soo-Hwang Teo Mary Beth Terry Mads Thomassen Laima Tihomirova Marc Tischkowitz Silvia Tognazzo Amanda Ewart Toland Nadine Tung Ans M W van den Ouweland Rob B van der Luijt Klaartje van Engelen Elizabeth J van Rensburg Raymonda Varon-Mateeva Barbara Wappenschmidt Juul T Wijnen Timothy Rebbeck Georgia Chenevix-Trench Kenneth Offit Fergus J Couch Silje Nord Douglas F Easton Antonis C Antoniou Jacques Simard

Breast Cancer Res Treat 2017 01 28;161(1):117-134. Epub 2016 Oct 28.

Genomics Center, Centre Hospitalier Universitaire de Québec Research Center and Laval University, 2705 Laurier Boulevard, Quebec, QC, G1V 4G2, Canada.

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http://dx.doi.org/10.1007/s10549-016-4018-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222911PMC
January 2017

Uniparental Disomy in Somatic Mosaicism 45,X/46,XY/46,XX Associated with Ambiguous Genitalia.

Sex Dev 2015 3;9(3):136-43. Epub 2015 Jun 3.

Division of Pediatric Surgery, Department of Surgery, University of Ulm, Ulm, Germany.

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http://dx.doi.org/10.1159/000430897DOI Listing
July 2016

De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.

Neurobiol Aging 2015 Nov 15;36(11):3117.e1-3117.e6. Epub 2015 Aug 15.

Institute of Human Genetics, University of Ulm, Ulm, Germany; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2015.08.005DOI Listing
November 2015

Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement.

Clin Dysmorphol 2015 Jan;24(1):17-20

aNeonatal Intensive Care Unit, Department of Mother and Child bMedical Genetics Unit, Department of Medical and Surgical Sciences cAudiology Unit, Department of Diagnostic Medicine, Clinical and Public Health, University of Modena, Modena dOtolaryngology Department, Community Healthcare Services, Modena, Italy eHuman Genetics, University of Ulm, Ulm, Germany.

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http://dx.doi.org/10.1097/MCD.0000000000000061DOI Listing
January 2015

C9ORF72-ALS: P62- and ubiquitin-aggregation pathology in skeletal muscle.

Muscle Nerve 2014 Sep;50(3):454-5

Department of Neurology, University of Erlangen-Nuremberg, Erlangen, Germany.

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http://dx.doi.org/10.1002/mus.24283DOI Listing
September 2014

Branchi-oculo-facial syndrome: a case report to highlight recent genetic considerations.

J Plast Reconstr Aesthet Surg 2012 Nov 24;65(11):1573-5. Epub 2012 Apr 24.

Surgical Department of Children's Hospital of Toulouse, 330, Avenue de Grande Bretagne, TSA 70034, 31059 Toulouse Cedex 9, France.

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http://dx.doi.org/10.1016/j.bjps.2012.03.045DOI Listing
November 2012

Craniofacial phenotype in the branchio-oculo-facial syndrome: four case reports.

Cleft Palate Craniofac J 2012 May 3;49(3):357-64. Epub 2011 May 3.

Department of Pediatric Maxillo-Facial and Plastic Surgery, Hôpital d'Enfant Armand-Trousseau, AP-HP, 26 Avenue du Dr. Arnold Netter, 75571, Paris, France.

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http://dx.doi.org/10.1597/10-203DOI Listing
May 2012

Sox9 gene regulation and the loss of the XY/XX sex-determining mechanism in the mole vole Ellobius lutescens.

Chromosome Res 2012 Jan;20(1):191-9

Molecular Genetics & Development Division, Prince Henry's Institute of Medical Research, Clayton, Melbourne, Victoria 3168, Australia.

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http://link.springer.com/10.1007/s10577-011-9269-5
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http://dx.doi.org/10.1007/s10577-011-9269-5DOI Listing
January 2012

Genetic polymorphisms in the formaldehyde dehydrogenase gene and their biological significance.

Toxicol Lett 2011 Nov 6;207(2):121-7. Epub 2011 Sep 6.

Universität Ulm, Institut für Humangenetik, Ulm, Germany.

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http://dx.doi.org/10.1016/j.toxlet.2011.08.025DOI Listing
November 2011

Exclusion of genes from the EYA-DACH-SIX-PAX pathway as candidates for Branchio-Oculo-Facial syndrome (BOFS).

Am J Med Genet A 2007 Sep;143A(18):2185-8

Institute of Human Genetics, University of Ulm, Ulm, Germany.

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http://dx.doi.org/10.1002/ajmg.a.31875DOI Listing
September 2007

Denys-Drash syndrome.

Medicina (Kaunas) 2005 ;41(2):132-4

Department of Human Genetics, Ulm University, Germany.

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February 2006

Human male sex determination and sexual differentiation: pathways, molecular interactions and genetic disorders.

Medicina (Kaunas) 2005 ;41(8):633-40

Department of Biology, Kaunas University of Medicine, Kaunas, Lithuania.

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February 2006

Higher aneuploidy rates of chromosomes 13, 16, and 21 in a patient with globozoospermia.

Fertil Steril 2005 Jul;84(1):217-8

Christian Lauritzen-Institut, University of Ulm, Ulm, Germany.

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http://dx.doi.org/10.1016/j.fertnstert.2005.01.109DOI Listing
July 2005

Characterization of Pisrt1/Foxl2 in Ellobius lutescens and exclusion as sex-determining genes.

Mamm Genome 2005 Apr;16(4):281-9

Department of Human Genetics, University of Ulm, Albert-Einstein-Allee 11, 89081, Ulm, Germany.

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http://dx.doi.org/10.1007/s00335-004-2019-7DOI Listing
April 2005

Sry does not fully sex-reverse female into male behavior towards pups.

Behav Genet 2002 Mar;32(2):103-11

Abteilung Anatomie und Zellbiologie, Universität Ulm, Germany.

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March 2002