P53 Binding Sites in Transposons

Por Zemojtel, Tomasz, Vingron, Martin
Publicado em 2012

L1Base: from functional annotation to prediction of active LINE-1 elements

Por Penzkofer, Tobias, Dandekar, Thomas, Zemojtel, Tomasz
Publicado em 2005

Exonization of active mouse L1s: a driver of transcriptome evolution?

Por Badge Richard, Dandekar Thomas, Schultz Jörg, Penzkofer Tobias, Zemojtel Tomasz, Vingron Martin
Publicado em 2007-10-01

Exonization of active mouse L1s: a driver of transcriptome evolution?

Por Zemojtel, Tomasz, Penzkofer, Tobias, Schultz, Jörg, Dandekar, Thomas, Badge, Richard, Vingron, Martin
Publicado em 2007

Rap1A-Deficient T and B Cells Show Impaired Integrin-Mediated Cell Adhesion

Por Duchniewicz, Marlena, Zemojtel, Tomasz, Kolanczyk, Mateusz, Grossmann, Steffen, Scheele, Jürgen S., Zwartkruis, Fried J. T.
Publicado em 2006

CpG Deamination Creates Transcription Factor–Binding Sites with High Efficiency

Por Żemojtel, Tomasz, kiełbasa, Szymon M., Arndt, Peter F., Behrens, Sarah, Bourque, Guillaume, Vingron, Martin
Publicado em 2011

Alternate-locus aware variant calling in whole genome sequencing

Por Jäger, Marten, Schubach, Max, Zemojtel, Tomasz, Reinert, Knut, Church, Deanna M., Robinson, Peter N.
Publicado no Genome Med (2016)

L1Base 2: more retrotransposition-active LINE-1s, more mammalian genomes

Por Penzkofer, Tobias, Jäger, Marten, Figlerowicz, Marek, Badge, Richard, Mundlos, Stefan, Robinson, Peter N., Zemojtel, Tomasz
Publicado no Nucleic Acids Res (2017)

Retrotransposition and mutation events yield Rap1 GTPases with differential signalling capacity

Por Zemojtel, Tomasz, Duchniewicz, Marlena, Zhang, Zhongchun, Paluch, Taisa, Luz, Hannes, Penzkofer, Tobias, Scheele, Jürgen S, Zwartkruis, Fried JT
Publicado em 2010

Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases

Por Smedley, Damian, Köhler, Sebastian, Czeschik, Johanna Christina, Amberger, Joanna, Bocchini, Carol, Hamosh, Ada, Veldboer, Julian, Zemojtel, Tomasz, Robinson, Peter N.
Publicado no Bioinformatics (2014)

Mutations in proteasome-related genes are associated with thyroid hemiagenesis

Por Budny, Bartlomiej, Szczepanek-Parulska, Ewelina, Zemojtel, Tomasz, Szaflarski, Witold, Rydzanicz, Malgorzata, Wesoly, Joanna, Handschuh, Luiza, Wolinski, Kosma, Piatek, Katarzyna, Niedziela, Marek, Ziemnicka, Katarzyna, Figlerowicz, Marek, Zabel, Maciej, Ruchala, Marek
Publicado no Endocrine (2017)

Next-generation diagnostics and disease-gene discovery with the Exomiser

Por Smedley, Damian, Jacobsen, Julius O B, Jager, Marten, Köhler, Sebastian, Holtgrewe, Manuel, Schubach, Max, Siragusa, Enrico, Zemojtel, Tomasz, Buske, Orion J, Washington, Nicole L, Bone, William P, Haendel, Melissa A, Robinson, Peter N
Publicado no Nat Protoc (2015)

PBX1 is dispensable for neural commitment of RA-treated murine ES cells

Por Jürgens, Anne S., Kolanczyk, Mateusz, Moebest, Dietrich C. C., Zemojtel, Tomasz, Lichtenauer, Urs, Duchniewicz, Marlena, Gantert, Melanie P., Hecht, Jochen, Hattenhorst, Uwe, Burdach, Stefan, Dorn, Annette, Kamps, Mark P., Beuschlein, Felix, Räpple, Daniel, Scheele, Jürgen S.
Publicado em 2009

MIA is a potential biomarker for tumour load in neurofibromatosis type 1

Por Kolanczyk, Mateusz, Mautner, Victor, Kossler, Nadine, Nguyen, Rosa, Kühnisch, Jirko, Zemojtel, Tomasz, Jamsheer, Aleksander, Wegener, Eike, Thurisch, Boris, Tinschert, Sigrid, Holtkamp, Nikola, Park, Su-Jin, Birch, Patricia, Kendler, David, Harder, Anja, Mundlos, Stefan, Kluwe, Lan
Publicado em 2011

The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies

Por Trubicka, Joanna, Żemojtel, Tomasz, Hecht, Jochen, Falana, Katarzyna, Piekutowska- Abramczuk, Dorota, Płoski, Rafał, Perek-Polnik, Marta, Drogosiewicz, Monika, Grajkowska, Wiesława, Ciara, Elżbieta, Moszczyńska, Elżbieta, Dembowska-Bagińska, Bożenna, Perek, Danuta, Chrzanowska, Krystyna H., Krajewska-Walasek, Małgorzata, Łastowska, Maria
Publicado no BMC Cancer (2017)

Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient

Por Emmerich, Denise, Zemojtel, Tomasz, Hecht, Jochen, Krawitz, Peter, Spielmann, Malte, Kühnisch, Jirko, Kobus, Karolina, Osswald, Monika, Heinrich, Verena, Berlien, Peter, Müller, Ute, Mautner, Victor-F, Wimmer, Katharina, Robinson, Peter N, Vingron, Martin, Tinschert, Sigrid, Mundlos, Stefan, Kolanczyk, Mateusz
Publicado no Eur J Hum Genet (2015)

A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease

Por Smedley, Damian, Schubach, Max, Jacobsen, Julius O.B., Köhler, Sebastian, Zemojtel, Tomasz, Spielmann, Malte, Jäger, Marten, Hochheiser, Harry, Washington, Nicole L., McMurry, Julie A., Haendel, Melissa A., Mungall, Christopher J., Lewis, Suzanna E., Groza, Tudor, Valentini, Giorgio, Robinson, Peter N.
Publicado no Am J Hum Genet (2016)

The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease

Por Groza, Tudor, Köhler, Sebastian, Moldenhauer, Dawid, Vasilevsky, Nicole, Baynam, Gareth, Zemojtel, Tomasz, Schriml, Lynn Marie, Kibbe, Warren Alden, Schofield, Paul N., Beck, Tim, Vasant, Drashtti, Brookes, Anthony J., Zankl, Andreas, Washington, Nicole L., Mungall, Christopher J., Lewis, Suzanna E., Haendel, Melissa A., Parkinson, Helen, Robinson, Peter N.
Publicado no Am J Hum Genet (2015)

NOA1 is an essential GTPase required for mitochondrial protein synthesis

Por Kolanczyk, Mateusz, Pech, Markus, Zemojtel, Tomasz, Yamamoto, Hiroshi, Mikula, Ivan, Calvaruso, Maria-Antonietta, van den Brand, Mariël, Richter, Ricarda, Fischer, Bjoern, Ritz, Anita, Kossler, Nadine, Thurisch, Boris, Spoerle, Ralf, Smeitink, Jan, Kornak, Uwe, Chan, Danny, Vingron, Martin, Martasek, Pavel, Lightowlers, Robert N., Nijtmans, Leo, Schuelke, Markus, Nierhaus, Knud H., Mundlos, Stefan
Publicado em 2011

Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome

Por Zemojtel, Tomasz, Köhler, Sebastian, Mackenroth, Luisa, Jäger, Marten, Hecht, Jochen, Krawitz, Peter, Graul-Neumann, Luitgard, Doelken, Sandra, Ehmke, Nadja, Spielmann, Malte, Øien, Nancy Christine, Schweiger, Michal R., Krüger, Ulrike, Frommer, Götz, Fischer, Björn, Kornak, Uwe, Flöttmann, Ricarda, Ardeshirdavani, Amin, Moreau, Yves, Lewis, Suzanna E., Haendel, Melissa, Smedley, Damian, Horn, Denise, Mundlos, Stefan, Robinson, Peter N.
Publicado no Sci Transl Med (2014)