Comparison among three variant callers and assessment of the accuracy of imputation from SNP array data to whole-genome sequence level in chicken

by Ni, Guiyan, Strom, Tim M., Pausch, Hubert, Reimer, Christian, Preisinger, Rudolf, Simianer, Henner, Erbe, Malena
Published 2015

Classic Selective Sweeps Revealed by Massive Sequencing in Cattle

by Qanbari, Saber, Pausch, Hubert, Jansen, Sandra, Somel, Mehmet, Strom, Tim M., Fries, Ruedi, Nielsen, Rasmus, Simianer, Henner
Published 2014

Genomic factors related to tissue tropism in Chlamydia pneumoniae infection

by Weinmaier, Thomas, Hoser, Jonathan, Eck, Sebastian, Kaufhold, Inga, Shima, Kensuke, Strom, Tim M, Rattei, Thomas, Rupp, Jan
Published 2015

A High Resolution Genome-Wide Scan for Significant Selective Sweeps: An Application to Pooled Sequence Data in Laying Chickens

by Qanbari, Saber, Strom, Tim M., Haberer, Georg, Weigend, Steffen, Gheyas, Almas A., Turner, Frances, Burt, David W., Preisinger, Rudolf, Gianola, Daniel, Simianer, Henner
Published 2012

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

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

Time- and compartment-resolved proteome profiling of the extracellular niche in lung injury and repair

by Schiller, Herbert B, Fernandez, Isis E, Burgstaller, Gerald, Schaab, Christoph, Scheltema, Richard A, Schwarzmayr, Thomas, Strom, Tim M, Eickelberg, Oliver, Mann, Matthias
Published 2015

Mutations at Ser331 in the HSN type I gene SPTLC1 are associated with a distinct syndromic phenotype

by Auer-Grumbach, Michaela, Bode, Heiko, Pieber, Thomas R., Schabhüttl, Maria, Fischer, Dirk, Seidl, Rainer, Graf, Elisabeth, Wieland, Thomas, Schuh, Reinhard, Vacariu, Gerda, Grill, Franz, Timmerman, Vincent, Strom, Tim M., Hornemann, Thorsten
Published 2013

Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndrome

by Haack, Tobias B., Makowski, Christine, Yao, Yoshiaki, Graf, Elisabeth, Hempel, Maja, Wieland, Thomas, Tauer, Ulrike, Ahting, Uwe, Mayr, Johannes A., Freisinger, Peter, Yoshimatsu, Hiroki, Inui, Ken, Strom, Tim M., Meitinger, Thomas, Yonezawa, Atsushi, Prokisch, Holger
Published 2012

Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families

by Shafique, Sobia, Siddiqi, Saima, Schraders, Margit, Oostrik, Jaap, Ayub, Humaira, Bilal, Ammad, Ajmal, Muhammad, Seco, Celia Zazo, Strom, Tim M., Mansoor, Atika, Mazhar, Kehkashan, Shah, Syed Tahir A., Hussain, Alamdar, Azam, Maleeha, Kremer, Hannie, Qamar, Raheel
Published 2014

Sequence variation between 462 human individuals fine-tunes functional sites of RNA processing

by Ferreira, Pedro G., Oti, Martin, Barann, Matthias, Wieland, Thomas, Ezquina, Suzana, Friedländer, Marc R., Rivas, Manuel A., Esteve-Codina, Anna, Rosenstiel, Philip, Strom, Tim M, Lappalainen, Tuuli, Guigó, Roderic, Sammeth, Michael
Published 2016

A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array

by Unterseer, Sandra, Bauer, Eva, Haberer, Georg, Seidel, Michael, Knaak, Carsten, Ouzunova, Milena, Meitinger, Thomas, Strom, Tim M, Fries, Ruedi, Pausch, Hubert, Bertani, Christofer, Davassi, Alessandro, Mayer, Klaus FX, Schön, Chris-Carolin
Published 2014

Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations

by Weegerink, Nicole J. D., Schraders, Margit, Oostrik, Jaap, Huygen, Patrick L. M., Strom, Tim M., Granneman, Susanne, Pennings, Ronald J. E., Venselaar, Hanka, Hoefsloot, Lies H., Elting, Mariet, Cremers, Cor W. R. J., Admiraal, Ronald J. C., Kremer, Hannie, Kunst, Henricus P. M.
Published 2011

Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping

by Siemiatkowska, Anna M., Arimadyo, Kentar, Moruz, Luminita M., Astuti, Galuh D.N., de Castro-Miro, Marta, Zonneveld, Marijke N., Strom, Tim M., de Wijs, Ilse J., Hoefsloot, Lies H., Faradz, Sultana M.H., Cremers, Frans P.M., den Hollander, Anneke I., Collin, Rob W.J.
Published 2011

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis

by Sabrautzki, Sibylle, Rubio-Aliaga, Isabel, Hans, Wolfgang, Fuchs, Helmut, Rathkolb, Birgit, Calzada-Wack, Julia, Cohrs, Christian M., Klaften, Matthias, Seedorf, Hartwig, Eck, Sebastian, Benet-Pagès, Ana, Favor, Jack, Esposito, Irene, Strom, Tim M., Wolf, Eckhard, Lorenz-Depiereux, Bettina, Hrabě de Angelis, Martin
Published 2012

MTO1 Mutations are Associated with Hypertrophic Cardiomyopathy and Lactic Acidosis and Cause Respiratory Chain Deficiency in Humans and Yeast

by Baruffini, Enrico, Dallabona, Cristina, Invernizzi, Federica, Yarham, John W, Melchionda, Laura, Blakely, Emma L, Lamantea, Eleonora, Donnini, Claudia, Santra, Saikat, Vijayaraghavan, Suresh, Roper, Helen P, Burlina, Alberto, Kopajtich, Robert, Walther, Anett, Strom, Tim M, Haack, Tobias B, Prokisch, Holger, Taylor, Robert W, Ferrero, Ileana, Zeviani, Massimo, Ghezzi, Daniele
Published 2013

Development of a high density 600K SNP genotyping array for chicken

by Kranis, Andreas, Gheyas, Almas A, Boschiero, Clarissa, Turner, Frances, Yu, Le, Smith, Sarah, Talbot, Richard, Pirani, Ali, Brew, Fiona, Kaiser, Pete, Hocking, Paul M, Fife, Mark, Salmon, Nigel, Fulton, Janet, Strom, Tim M, Haberer, Georg, Weigend, Steffen, Preisinger, Rudolf, Gholami, Mahmood, Qanbari, Saber, Simianer, Henner, Watson, Kellie A, Woolliams, John A, Burt, David W
Published 2013

Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

by Weisschuh, Nicole, Mayer, Anja K., Strom, Tim M., Kohl, Susanne, Glöckle, Nicola, Schubach, Max, Andreasson, Sten, Bernd, Antje, Birch, David G., Hamel, Christian P., Heckenlively, John R., Jacobson, Samuel G., Kamme, Christina, Kellner, Ulrich, Kunstmann, Erdmute, Maffei, Pietro, Reiff, Charlotte M., Rohrschneider, Klaus, Rosenberg, Thomas, Rudolph, Günther, Vámos, Rita, Varsányi, Balázs, Weleber, Richard G., Wissinger, Bernd
Published 2016

Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis

by Sabrautzki, Sibylle, Rubio-Aliaga, Isabel, Hans, Wolfgang, Fuchs, Helmut, Rathkolb, Birgit, Calzada-Wack, Julia, Cohrs, Christian M., Klaften, Matthias, Seedorf, Hartwig, Eck, Sebastian, Benet-Pagès, Ana, Favor, Jack, Esposito, Irene, Strom, Tim M., Wolf, Eckhard, Lorenz-Depiereux, Bettina, Hrabĕ de Angelis, Martin
Published 2014

HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome

by Hollstein, Ronja, Parry, David A, Nalbach, Lisa, Logan, Clare V, Strom, Tim M, Hartill, Verity L, Carr, Ian M, Korenke, Georg C, Uppal, Sandeep, Ahmed, Mushtaq, Wieland, Thomas, Markham, Alexander F, Bennett, Christopher P, Gillessen-Kaesbach, Gabriele, Sheridan, Eamonn G, Kaiser, Frank J, Bonthron, David T
Published 2015

VARS2 and TARS2 Mutations in Patients with Mitochondrial Encephalomyopathies

by Diodato, Daria, Melchionda, Laura, Haack, Tobias B, Dallabona, Cristina, Baruffini, Enrico, Donnini, Claudia, Granata, Tiziana, Ragona, Francesca, Balestri, Paolo, Margollicci, Maria, Lamantea, Eleonora, Nasca, Alessia, Powell, Christopher A, Minczuk, Michal, Strom, Tim M, Meitinger, Thomas, Prokisch, Holger, Lamperti, Costanza, Zeviani, Massimo, Ghezzi, Daniele
Published 2014