STAT3 single-nucleotide polymorphisms and STAT3 mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma families

Por Wjst, Matthias, Lichtner, Peter, Meitinger, Thomas, Grimbacher, Bodo
Publicado em 2009

The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase

Por Linari, Marco, Ueffing, Marius, Manson, Forbes, Wright, Alan, Meitinger, Thomas, Becker, Jörg
Publicado em 1999

Genome-wide association studies of atrial fibrillation: past, present, and future

Por Sinner, Moritz F., Ellinor, Patrick T., Meitinger, Thomas, Benjamin, Emelia J., Kääb, Stefan
Publicado em 2011

Effect of genome-wide simultaneous hypotheses tests on the discovery rate

Por Eyheramendy, Susana, Gieger, Christian, Laan, Maris, Illig, Thomas, Meitinger, Thomas, Wichmann, Erich
Publicado em 2011

A One Base Pair Deletion in the Canine ATP13A2 Gene Causes Exon Skipping and Late-Onset Neuronal Ceroid Lipofuscinosis in the Tibetan Terrier

Por Wöhlke, Anne, Philipp, Ute, Bock, Patricia, Beineke, Andreas, Lichtner, Peter, Meitinger, Thomas, Distl, Ottmar
Publicado em 2011

Whole genome sequencing of a single Bos taurus animal for single nucleotide polymorphism discovery

Por Eck, Sebastian H, Benet-Pagès, Anna, Flisikowski, Krzysztof, Meitinger, Thomas, Fries, Ruedi, Strom, Tim M
Publicado em 2009

Impairment of Drosophila Orthologs of the Human Orphan Protein C19orf12 Induces Bang Sensitivity and Neurodegeneration

Por Iuso, Arcangela, Sibon, Ody C. M., Gorza, Matteo, Heim, Katharina, Organisti, Cristina, Meitinger, Thomas, Prokisch, Holger
Publicado em 2014

Mitochondrial Genetic Variants Identified to Be Associated with BMI in Adults

Por Flaquer, Antònia, Baumbach, Clemens, Kriebel, Jennifer, Meitinger, Thomas, Peters, Annette, Waldenberger, Melanie, Grallert, Harald, Strauch, Konstantin
Publicado em 2014

Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia

Por Gawlik Micha, Rubie Claudia, Siekiera Markus, Kohlmann Bernd, Stöber Gerald, Möller-Ehrlich Kerstin, Meitinger Thomas, Bettecken Thomas
Publicado em 2005-10-01

Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia

Por Stöber, Gerald, Kohlmann, Bernd, Siekiera, Markus, Rubie, Claudia, Gawlik, Micha, Möller-Ehrlich, Kerstin, Meitinger, Thomas, Bettecken, Thomas
Publicado em 2005

Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limb

Por Umair, Muhammad, Shah, Khadim, Alhaddad, Bader, Haack, Tobias B, Graf, Elisabeth, Strom, Tim M, Meitinger, Thomas, Ahmad, Wasim
Publicado no Eur J Hum Genet (2017)

Mitochondrial GWA Analysis of Lipid Profile Identifies Genetic Variants to Be Associated with HDL Cholesterol and Triglyceride Levels

Por Flaquer, Antònia, Rospleszcz, Susanne, Reischl, Eva, Zeilinger, Sonja, Prokisch, Holger, Meitinger, Thomas, Meisinger, Christa, Peters, Annette, Waldenberger, Melanie, Grallert, Harald, Strauch, Konstantin
Publicado no PLoS One (2015)

Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9

Por Danhauser, Katharina, Herebian, Diran, Haack, Tobias B, Rodenburg, Richard J, Strom, Tim M, Meitinger, Thomas, Klee, Dirk, Mayatepek, Ertan, Prokisch, Holger, Distelmaier, Felix
Publicado no Eur J Hum Genet (2016)

Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation

Por Wagenstaller, Janine , Spranger, Stephanie , Lorenz-Depiereux, Bettina , Kazmierczak, Bernd , Nathrath, Michaela , Wahl, Dagmar , Heye, Babett , Gläser, Dieter , Liebscher, Volkmar , Meitinger, Thomas , Strom, Tim M. 
Publicado em 2007

A multimetric approach to analysis of genome-wide association by single markers and composite likelihood

Por Gibson, Jane, Tapper, William, Cox, David, Zhang, Weihua, Pfeufer, Arne, Gieger, Christian, Wichmann, H.-Erich, Kääb, Stefan, Collins, Andrew R., Meitinger, Thomas, Morton, Newton
Publicado em 2008

Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage

Por Jansen, Sandra, Aigner, Bernhard, Pausch, Hubert, Wysocki, Michal, Eck, Sebastian, Benet-Pagès, Anna, Graf, Elisabeth, Wieland, Thomas, Strom, Tim M, Meitinger, Thomas, Fries, Ruedi
Publicado em 2013

Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction

Por Brænne, Ingrid, Kleinecke, Mariana, Reiz, Benedikt, Graf, Elisabeth, Strom, Tim, Wieland, Thomas, Fischer, Marcus, Kessler, Thorsten, Hengstenberg, Christian, Meitinger, Thomas, Erdmann, Jeanette, Schunkert, Heribert
Publicado no Eur J Hum Genet (2016)

Genetic Variants Associated With Atrial Fibrillation and PR Interval Following Cardiac Surgery

Por Sigurdsson, Martin I., Muehlschlegel, Jochen D., Fox, Amanda A., Heydarpour, Mahyar, Lichtner, Peter, Meitinger, Thomas, Collard, Charles D., Shernan, Stanton K., Body, Simon C.
Publicado no J Cardiothorac Vasc Anesth (2014)

A Systematic Evaluation of Short Tandem Repeats in Lipid Candidate Genes: Riding on the SNP-Wave

Por Lamina, Claudia, Haun, Margot, Coassin, Stefan, Kloss-Brandstätter, Anita, Gieger, Christian, Peters, Annette, Grallert, Harald, Strauch, Konstantin, Meitinger, Thomas, Kedenko, Lyudmyla, Paulweber, Bernhard, Kronenberg, Florian
Publicado em 2014

A mutation screening of oncogenes, tumor suppressor gene TP53 and nuclear encoded mitochondrial complex I genes in oncocytic thyroid tumors

Por Evangelisti, Cecilia, de Biase, Dario, Kurelac, Ivana, Ceccarelli, Claudio, Prokisch, Holger, Meitinger, Thomas, Caria, Paola, Vanni, Roberta, Romeo, Giovanni, Tallini, Giovanni, Gasparre, Giuseppe, Bonora, Elena
Publicado no BMC Cancer (2015)