Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia
Bergmann, Carsten, Fliegauf, Manfred, Brüchle, Nadina Ortiz, Frank, Valeska, Olbrich, Heike, Kirschner, Jan, Schermer, Bernhard, Schmedding, Ingolf, Kispert, Andreas, Kränzlin, Bettina, Nürnberg, Gudrun, Becker, Christian, Grimm, Tiemo, Girschick, Gundula, Lynch, Sally A., Kelehan, Peter, Senderek, Jan, Neuhaus, Thomas J., Stallmach, Thomas, Zentgraf, Hanswalter, Nürnberg, Peter, Gretz, Norbert, Lo, Cecilia, Lienkamp, Soeren, Schäfer, Tobias, Walz, Gerd, Benzing, Thomas, Zerres, Klaus, Omran, Heymut
Published in American journal of human genetics (01.04.2008)
Published in American journal of human genetics (01.04.2008)
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Journal Article
PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption
Decker, Eva, Stellzig-Eisenhauer, Angelika, Fiebig, Britta S., Rau, Christiane, Kress, Wolfram, Saar, Kathrin, Rüschendorf, Franz, Hubner, Norbert, Grimm, Tiemo, Weber, Bernhard H.F.
Published in American journal of human genetics (01.12.2008)
Published in American journal of human genetics (01.12.2008)
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Journal Article
Humangenetische Beratung in Deutschland: Entwicklung der Inanspruchnahme
Schmidtke, Jörg, Epplen, Jörg T., Glaubitz, Ralf, Grimm, Tiemo, Nippert, R. Peter, Tönnies, Holger, Zerres, Klaus, Nippert, Irmgard
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01.09.2020)
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01.09.2020)
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Journal Article
Primary Failure of Eruption (PFE) – Clinical and Molecular Genetics Analysis
Stellzig-Eisenhauer, Angelika, Decker, Eva, Meyer-Marcotty, Philipp, Rau, Christiane, Fiebig, Britta S., Kress, Wolfram, Saar, Kathrin, Rüschendorf, Franz, Hubner, Norbert, Grimm, Tiemo, Witt, Emil, Weber, Bernhard H. F.
Published in Journal of orofacial orthopedics (2010)
Published in Journal of orofacial orthopedics (2010)
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Journal Article
Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer Consortium
Fischer, Christine, Kuchenbäcker, Karoline, Engel, Christoph, Zachariae, Silke, Rhiem, Kerstin, Meindl, Alfons, Rahner, Nils, Dikow, Nicola, Plendl, Hansjörg, Debatin, Irmgard, Grimm, Tiemo, Gadzicki, Dorothea, Flöttmann, Ricarda, Horvath, Judit, Schröck, Evelin, Stock, Friedrich, Schäfer, Dieter, Schwaab, Ira, Kartsonaki, Christiana, Mavaddat, Nasim, Schlegelberger, Brigitte, Antoniou, Antonis C, Schmutzler, Rita
Published in Journal of medical genetics (01.06.2013)
Published in Journal of medical genetics (01.06.2013)
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Journal Article
Validation of the Manchester scoring system for predicting BRCA1/2 mutations in 9,390 families suspected of having hereditary breast and ovarian cancer
Kast, Karin, Schmutzler, Rita K., Rhiem, Kerstin, Kiechle, Marion, Fischer, Christine, Niederacher, Dieter, Arnold, Norbert, Grimm, Tiemo, Speiser, Dorothee, Schlegelberger, Brigitte, Varga, Dominic, Horvath, Judit, Beer, Marit, Briest, Susanne, Meindl, Alfons, Engel, Christoph
Published in International journal of cancer (15.11.2014)
Published in International journal of cancer (15.11.2014)
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Journal Article
Genetic counseling in Germany: development of demand
Schmidtke, Jörg, Epplen, Jörg T, Glaubitz, Ralf, Grimm, Tiemo, Nippert, R Peter, Tönnies, Holger, Zerres, Klaus, Nippert, Irmgard
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01.09.2020)
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01.09.2020)
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Journal Article
Risk assessment and genetic counseling in families with Duchenne muscular dystrophy
Grimm, Tiemo, Kress, Wolfram, Meng, Gerhard, Müller, Clemens R
Published in Acta myologica (01.12.2012)
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Published in Acta myologica (01.12.2012)
Journal Article
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q
Grimm, Tiemo, Garshasbi, Masoud, Puettmann, Lucia, Chen, Wei, Ullmann, Reinhard, Müller-Myhsok, Bertram, Klopocki, Eva, Herbst, Lina, Haug, Janina, Jensen, Lars R, Fischer, Christine, Nöthen, Markus, Ludwig, Kerstin, Warnke, Andreas, Ott, Jürg, Schulte-Körne, Gerd, Ropers, Hans-Hilger, Kuss, Andreas W
Published in Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie (01.11.2020)
Published in Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie (01.11.2020)
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Journal Article
Funktioniert die Informationsweitergabe in Familien mit erblichem Brust- und Eierstockkrebs?
Scholl, Eva, Grimm, Tiemo, Krockenberger, Mathias, Kunstmann, Erdmute
Published in Medizinische Genetik (01.08.2015)
Published in Medizinische Genetik (01.08.2015)
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Journal Article
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21
König, Inke R., Schumacher, Johannes, Hoffmann, Per, Kleensang, André, Ludwig, Kerstin U., Grimm, Tiemo, Neuhoff, Nina, Preis, Maike, Roeske, Darina, Warnke, Andreas, Propping, Peter, Remschmidt, Helmut, Nöthen, Markus M., Ziegler, Andreas, Müller-Myhsok, Bertram, Schulte-Körne, Gerd
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2011)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2011)
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Journal Article
Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a SOD-1 Mutation: Potential Impact of CNTF as a Candidate Modifier Gene
Giess, Ralf, Holtmann, Bettina, Braga, Massimiliano, Grimm, Tiemo, Müller-Myhsok, Bertram, Toyka, Klaus V., Sendtner, Michael
Published in American journal of human genetics (01.05.2002)
Published in American journal of human genetics (01.05.2002)
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Journal Article
Association of homozygous LMNA mutation R471C with new phenotype: Mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy
Zirn, Birgit, Kress, Wolfram, Grimm, Tiemo, Berthold, Lars Daniel, Neubauer, Bernd, Kuchelmeister, Klaus, Müller, Ulrich, Hahn, Andreas
Published in American journal of medical genetics. Part A (15.04.2008)
Published in American journal of medical genetics. Part A (15.04.2008)
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Journal Article