A-T(Winnipeg): Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening r...

por Nakamura, Kotoka, Fike, Francesca, Haghayegh, Sara, Saunders-Pullman, Rachel, Dawson, Angelika J, Dörk, Thilo, Gatti, Richard A
Publicado 2014

Characterization of a Novel Third-Generation Anti-CD24-CAR against Ovarian Cancer

por Klapdor, Rüdiger, Wang, Shuo, Morgan, Michael, Dörk, Thilo, Hacker, Ulrich, Hillemanns, Peter, Büning, Hildegard, Schambach, Axel
Publicado 2019

Human RAD50 deficiency: Confirmation of a distinctive phenotype

por Ragamin, Aviël, Yigit, Gökhan, Bousset, Kristine, Beleggia, Filippo, Verheijen, Frans W., de Wit, Marie‐Claire Y., Strom, Tim M., Dörk, Thilo, Wollnik, Bernd, Mancini, Grazia M. S.
Publicado 2020

Genetic association study of fatal pulmonary embolism

por Meißner, Lisa, Schürmann, Peter, Dörk, Thilo, Hagemeier, Lars, Klintschar, Michael
Publicado 2020

Tyrosine kinase inhibitors targeting vascular endothelial growth factor and the risk of aortic dissection—A pharmacovigilance analysis

por Dörks, Michael, Jobski, Kathrin, Herget‐Rosenthal, Stefan, Hoffmann, Falk, Douros, Antonios
Publicado 2021

Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS)

por Kerz, J., Schürmann, P., Rothämel, T., Dörk, T., Klintschar, M.
Publicado 2021

Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility

por Kho, Pik Fang, Wang, Xuemin, Cuéllar-Partida, Gabriel, Dörk, Thilo, Goode, Ellen L., Lambrechts, Diether, Scott, Rodney J., Spurdle, Amanda B., O’Mara, Tracy A., Glubb, Dylan M.
Publicado 2021

Cancer in Children With Fanconi Anemia and Ataxia-Telangiectasia—A Nationwide Register-Based Cohort Study in Germany

por Dutzmann, Christina M., Spix, Claudia, Popp, Isabell, Kaiser, Melanie, Erdmann, Friederike, Erlacher, Miriam, Dörk, Thilo, Schindler, Detlev, Kalb, Reinhard, Kratz, Christian P.
Publicado 2022

Targeted next-generation sequencing of 21 candidate genes in hereditary ovarian cancer patients from the Republic of Bashkortostan

por Prokofyeva, D. S., Mingazheva, E. T., Valova, Ya. V., Sakaeva, D. D., Faishanova, R. R., Nurgalieva, A. Kh., Valiev, R. R., Bogdanova, N., Dörk, T., Khusnutdinova, E. K.
Publicado 2023

ATM polymorphisms as risk factors for prostate cancer development

por Angèle, S, Falconer, A, Edwards, S M, Dörk, T, Bremer, M, Moullan, N, Chapot, B, Muir, K, Houlston, R, Norman, A R, Bullock, S, Hope, Q, Meitz, J, Dearnaley, D, Dowe, A, Southgate, C, Ardern-Jones, A, Easton, D F, Eeles, R A, Hall, J
Publicado 2004

Expression of Tas1 Taste Receptors in Mammalian Spermatozoa: Functional Role of Tas1r1 in Regulating Basal Ca(2+) and cAMP Concentrations in Spermatozoa

por Meyer, Dorke, Voigt, Anja, Widmayer, Patricia, Borth, Heike, Huebner, Sandra, Breit, Andreas, Marschall, Susan, de Angelis, Martin Hrabé, Boehm, Ulrich, Meyerhof, Wolfgang, Gudermann, Thomas, Boekhoff, Ingrid
Publicado 2012

Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer

por Kohlhase, Sandra, Bogdanova, Natalia V., Schürmann, Peter, Bermisheva, Marina, Khusnutdinova, Elza, Antonenkova, Natalia, Park-Simon, Tjoung-Won, Hillemanns, Peter, Meyer, Andreas, Christiansen, Hans, Schindler, Detlev, Dörk, Thilo
Publicado 2014

Functional deficiency of NBN, the Nijmegen breakage syndrome protein, in a p.R215W mutant breast cancer cell line

por Schröder-Heurich, Bianca, Bogdanova, Natalia, Wieland, Britta, Xie, Xiaoxi, Noskowicz, Monika, Park-Simon, Tjoung-Won, Hillemanns, Peter, Christiansen, Hans, Dörk, Thilo
Publicado 2014

Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649)

por Knappskog, Stian, Gansmo, Liv B., Dibirova, Khadizha, Metspalu, Andres, Cybulski, Cezary, Peterlongo, Paolo, Aaltonen, Lauri, Vatten, Lars, Romundstad, Pål, Hveem, Kristian, Devilee, Peter, Evans, Gareth D., Lin, Dongxin, Camp, Guy Van, Manolopoulos, Vangelis G., Osorio, Ana, Milani, Lili, Ozcelik, Tayfun, Zalloua, Pierre, Mouzaya, Francis, Bliznetz, Elena, Balanovska, Elena, Pocheshkova, Elvira, Kučinskas, Vaidutis, Atramentova, Lubov, Nymadawa, Pagbajabyn, Titov, Konstantin, Lavryashina, Maria, Yusupov, Yuldash, Bogdanova, Natalia, Koshel, Sergey, Zamora, Jorge, Wedge, David C., Charlesworth, Deborah, Dörk, Thilo, Balanovsky, Oleg, Lønning, Per E.
Publicado 2014

Recreational physical inactivity and mortality in women with invasive epithelial ovarian cancer: evidence from the Ovarian Cancer Association Consortium

por Cannioto, Rikki A, LaMonte, Michael J, Kelemen, Linda E, Risch, Harvey A, Eng, Kevin H, Minlikeeva, Albina N, Hong, Chi-Chen, Szender, J Brian, Sucheston-Campbell, Lara, Joseph, Janine M, Berchuck, Andrew, Chang-Claude, Jenny, Cramer, Daniel W, DeFazio, Anna, Diergaarde, Brenda, Dörk, Thilo, Doherty, Jennifer A, Edwards, Robert P, Fridley, Brooke L, Friel, Grace, Goode, Ellen L, Goodman, Marc T, Hillemanns, Peter, Hogdall, Estrid, Hosono, Satoyo, Kelley, Joseph L, Kjaer, Susanne K, Klapdor, Rüdiger, Matsuo, Keitaro, Odunsi, Kunle, Nagle, Christina M, Olsen, Catherine M, Paddock, Lisa E, Pearce, Celeste L, Pike, Malcolm C, Rossing, Mary A, Schmalfeldt, Barbara, Segal, Brahm H, Szamreta, Elizabeth A, Thompson, Pamela J, Tseng, Chiu-Chen, Vierkant, Robert, Schildkraut, Joellen M, Wentzensen, Nicolas, Wicklund, Kristine G, Winham, Stacey J, Wu, Anna H, Modugno, Francesmary, Ness, Roberta B, Jensen, Allan, Webb, Penelope M, Terry, Kathryn, Bandera, Elisa V, Moysich, Kirsten B
Publicado 2016

History of thyroid disease and survival of ovarian cancer patients: results from the Ovarian Cancer Association Consortium, a brief report

por Minlikeeva, Albina N, Freudenheim, Jo L, Cannioto, Rikki A, Eng, Kevin H, Szender, J Brian, Mayor, Paul, Etter, John L, Cramer, Daniel W, Diergaarde, Brenda, Doherty, Jennifer A, Dörk, Thilo, Edwards, Robert, deFazio, Anna, Friel, Grace, Goodman, Marc T, Hillemanns, Peter, Høgdall, Estrid, Jensen, Allan, Jordan, Susan J, Karlan, Beth Y, Kjær, Susanne K, Klapdor, Rüdiger, Matsuo, Keitaro, Mizuno, Mika, Nagle, Christina M, Odunsi, Kunle, Paddock, Lisa, Rossing, Mary Anne, Schildkraut, Joellen M, Schmalfeldt, Barbara, Segal, Brahm H, Starbuck, Kristen, Terry, Kathryn L, Webb, Penelope M, Zsiros, Emese, Ness, Roberta B, Modugno, Francesmary, Bandera, Elisa V, Chang-Claude, Jenny, Moysich, Kirsten B
Publicado 2017

Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling

por Richter, Melanie, Murtaza, Nadeem, Scharrenberg, Robin, White, Sean H., Johanns, Ole, Walker, Susan, Yuen, Ryan K. C., Schwanke, Birgit, Bedürftig, Bianca, Henis, Melad, Scharf, Sarah, Kraus, Vanessa, Dörk, Ronja, Hellmann, Jakob, Lindenmaier, Zsuzsa, Ellegood, Jacob, Hartung, Henrike, Kwan, Vickie, Sedlacik, Jan, Fiehler, Jens, Schweizer, Michaela, Lerch, Jason P., Hanganu-Opatz, Ileana L., Morellini, Fabio, Scherer, Stephen W., Singh, Karun K., Calderon de Anda, Froylan
Publicado 2018

Regional Differences in Opioid Prescribing in Germany – Results of an Analysis of Health Insurance Data of 57 Million Adult People

por Jobski, Kathrin, Dörks, Michael, Bantel, Carsten, Hoffmann, Falk
Publicado 2020

Germline variation of Ribonuclease H2 genes in ovarian cancer patients

por Polaczek, Rahel, Schürmann, Peter, Speith, Lisa-Marie, Geffers, Robert, Dürst, Matthias, Hillemanns, Peter, Park-Simon, Tjoung-Won, Liebrich, Clemens, Dörk, Thilo
Publicado 2020

Variants in genes encoding the SUR1-TRPM4 non-selective cation channel and sudden infant death syndrome (SIDS): potentially increased risk for cerebral edema

por Qu, Dong, Schürmann, Peter, Rothämel, Thomas, Dörk, Thilo, Klintschar, Michael
Publicado 2022