Search Results - Reis, André

Identification of two genetic loci associated with leukopenia after chemotherapy in patients with breast cancer by Fasching, Peter Andreas (Author) , Liu, Duan (Author) , Scully, Steve (Author) , Ingle, James N. (Author) , Lyra, Paulo C., Jr. (Author) , Rack, Brigitte (Author) , Hein, Alexander (Author) , Ekici, Arif B. (Author) , Reis, Andre (Author) , Schneeweiss, Andreas (Author) , Tesch, Hans (Author) , Fehm, Tanja N. (Author) , Heinrich, Georg (Author) , Beckmann, Matthias W. (Author) , Ruebner, Matthias (Author) , Huebner, Hanna (Author) , Lambrechts, Diether (Author) , Madden, Ebony (Author) , Shen, Jess (Author) , Romm, Jane (Author) , Doheny, Kim (Author) , Jenkins, Gregory D. (Author) , Carlson, Erin E. (Author) , Li, Liang (Author) , Fridley, Brooke L. (Author) , Cunningham, Julie M. (Author) , Janni, Wolfgang (Author) , Monteiro, Alvaro N.A. (Author) , Schaid, Daniel J. (Author) , Häberle, Lothar (Author) , Weinshilboum, Richard M. (Author) , Wang, Liewei (Author) ,

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De novo missense variants in FBXO11 alter its protein expression and subcellular localization by Gregor, Anne (Author) , Meerbrei, Tanja (Author) , Gerstner, Thorsten (Author) , Toutain, Annick (Author) , Lynch, Sally Ann (Author) , Stals, Karen (Author) , Maxton, Caroline (Author) , Lemke, Johannes R. (Author) , Bernat, John A. (Author) , Bombei, Hannah M. (Author) , Foulds, Nicola (Author) , Hunt, David (Author) , Kuechler, Alma (Author) , Beygo, Jasmin (Author) , Stobe, Petra (Author) , Bouman, Arjan (Author) , Palomares-Bralo, Maria (Author) , Santos-Simarro, Fernando (Author) , Garcia-Minaur, Sixto (Author) , Pacio-Miguez, Marta (Author) , Popp, Bernt (Author) , Vasileiou, Georgia (Author) , Hebebrand, Moritz (Author) , Reis, Andre (Author) , Schuhmann, Sarah (Author) , Krumbiegel, Mandy (Author) , Brown, Natasha J. (Author) , Sparber, Peter (Author) , Melikyan, Lyusya (Author) , Bessonova, Liudmila (Author) , Cherevatova, Tatiana (Author) , Sharkov, Artem (Author) , Shcherbakova, Natalia (Author) , Dabir, Tabib (Author) , Kini, Usha (Author) , Schwaibold, Eva (Author) , Haack, Tobias B. (Author) , Bertoli, Marta (Author) , Hoffjan, Sabine (Author) , Falb, Ruth (Author) , Shinawi, Marwan (Author) , Sticht, Heinrich (Author) , Zweier, Christiane (Author) ,

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Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling by Holtz, Alexander M. (Author) , VanCoillie, Rachel (Author) , Vansickle, Elizabeth A. (Author) , Carere, Deanna Alexis (Author) , Withrow, Kara (Author) , Torti, Erin (Author) , Juusola, Jane (Author) , Millan, Francisca (Author) , Person, Richard (Author) , Guillen Sacoto, Maria J. (Author) , Si, Yue (Author) , Wentzensen, Ingrid M. (Author) , Pugh, Jada (Author) , Vasileiou, Georgia (Author) , Rieger, Melissa (Author) , Reis, André (Author) , Argilli, Emanuela (Author) , Sherr, Elliott H. (Author) , Aldinger, Kimberly A. (Author) , Dobyns, William B. (Author) , Brunet, Theresa (Author) , Hoefele, Julia (Author) , Wagner, Matias (Author) , Haber, Benjamin (Author) , Kotzaeridou, Urania (Author) , Keren, Boris (Author) , Heron, Delphine (Author) , Mignot, Cyril (Author) , Heide, Solveig (Author) , Courtin, Thomas (Author) , Buratti, Julien (Author) , Murugasen, Serini (Author) , Donald, Kirsten A. (Author) , O’Heir, Emily (Author) , Moody, Shade (Author) , Kim, Katherine H. (Author) , Burton, Barbara K. (Author) , Yoon, Grace (Author) , Campo, Miguel del (Author) , Masser-Frye, Diane (Author) , Kozenko, Mariya (Author) , Parkinson, Christina (Author) , Sell, Susan L. (Author) , Gordon, Patricia L. (Author) , Prokop, Jeremy W. (Author) , Karaa, Amel (Author) , Bupp, Caleb (Author) , Raby, Benjamin A. (Author) ,

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Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases by Wopperer, Florian (Author) , Knaup, Karl X. (Author) , Stanzick, Kira J. (Author) , Schneider, Karen (Author) , Jobst-Schwan, Tilman (Author) , Ekici, Arif B. (Author) , Uebe, Steffen (Author) , Wenzel, Andrea (Author) , Schliep, Stefan (Author) , Schürfeld, Carsten (Author) , Seitz, Randolf (Author) , Bernhardt, Wanja (Author) , Gödel, Markus (Author) , Wiesener, Antje (Author) , Popp, Bernt (Author) , Stark, Klaus J. (Author) , Gröne, Hermann-Josef (Author) , Friedrich, Björn (Author) , Weiß, Martin (Author) , Basic-Jukic, Nikolina (Author) , Schiffer, Mario (Author) , Schröppel, Bernd (Author) , Huettel, Bruno (Author) , Beck, Bodo B. (Author) , Sayer, John A. (Author) , Ziegler, Christine (Author) , Büttner-Herold, Maike (Author) , Amann, Kerstin (Author) , Heid, Iris M. (Author) , Reis, André (Author) , Pasutto, Francesca (Author) , Wiesener, Michael S. (Author) ,

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Genetic analysis of MPO variants in four psoriasis subtypes in patients from Germany by Haskamp, Stefan (Author) , Horowitz, Joseph Simon (Author) , Oji, Vinzenz (Author) , Philipp, Sandra (Author) , Sticherling, Michael (Author) , Schäkel, Knut (Author) , Schuhmann, Sarah Laetissia (Author) , Prinz, Jörg C. (Author) , Burkhardt, Harald (Author) , Behrens, Frank (Author) , Böhm, Beate (Author) , Köhm, Michaela (Author) , Rech, Jürgen (Author) , Simon, David (Author) , Schett, Georg (Author) , Morrison, Kirsten (Author) , Gerdes, Sascha (Author) , Assmann, Gunter (Author) , Nimeh, Ali (Author) , Schuster, Volker (Author) , Jacobi, Arnd (Author) , Weyergraf, Ansgar (Author) , Reis, André (Author) , Uebe, Steffen (Author) , Wilsmann-Theis, Dagmar (Author) , Mößner, Rotraut (Author) , Hüffmeier, Ulrike (Author) ,

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Mutations in BRCA1/2 and other panel genes in patients with metastatic breast cancer: association with patient and disease characteristics and effect on prognosis by Fasching, Peter Andreas (Author) , Yadav, Siddhartha (Author) , Hu, Chunling (Author) , Wunderle, Marius (Author) , Häberle, Lothar (Author) , Hart, Steven N. (Author) , Rübner, Matthias (Author) , Polley, Eric C. (Author) , Lee, Kun Y. (Author) , Gnanaolivu, Rohan D. (Author) , Hadji, Peyman (Author) , Hübner, Hanna (Author) , Tesch, Hans (Author) , Ettl, Johannes (Author) , Overkamp, Friedrich (Author) , Lux, Michael P. (Author) , Ekici, Arif B. (Author) , Volz, Bernhard (Author) , Uhrig, Sabrina (Author) , Lüftner, Diana (Author) , Wallwiener, Markus (Author) , Müller, Volkmar (Author) , Belleville, Erik (Author) , Untch, Michael (Author) , Kolberg, Hans-Christian (Author) , Beckmann, Matthias W. (Author) , Reis, André (Author) , Hartmann, Arndt (Author) , Janni, Wolfgang (Author) , Wimberger, Pauline (Author) , Taran, Florin-Andrei (Author) , Fehm, Tanja (Author) , Wallwiener, Diethelm (Author) , Brucker, Sara (Author) , Schneeweiss, Andreas (Author) , Hartkopf, Andreas (Author) , Couch, Fergus J. (Author) ,

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Myeloperoxidase modulates inflammation in generalized pustular psoriasis and additional rare pustular skin diseases by Haskamp, Stefan (Author) , Bruns, Heiko (Author) , Hahn, Madelaine (Author) , Hoffmann, Markus (Author) , Gregor, Anne (Author) , Löhr, Sabine (Author) , Hahn, Jonas (Author) , Schauer, Christine (Author) , Ringer, Mark (Author) , Flamann, Cindy (Author) , Frey, Benjamin (Author) , Lesner, Adam (Author) , Thiel, Christian T. (Author) , Ekici, Arif Bülent (Author) , Hörsten, Stephan von (Author) , Aßmann, Gunter (Author) , Riepe, Claudia (Author) , Euler, Maximilien (Author) , Schäkel, Knut (Author) , Philipp, Sandra (Author) , Prinz, Jörg C. (Author) , Mößner, Rotraut (Author) , Kersting, Florina (Author) , Sticherling, Michael (Author) , Sefiani, Abdelaziz (Author) , Lyahyai, Jaber (Author) , Sondermann, Wiebke (Author) , Oji, Vinzenz (Author) , Schulz, Peter (Author) , Wilsmann-Theis, Dagmar Irmgard (Author) , Sticht, Heinrich (Author) , Schett, Georg (Author) , Reis, André (Author) , Uebe, Steffen (Author) , Frey, Silke (Author) , Hüffmeier, Ulrike (Author) ,

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Evidence for genetic overlap between adult onset Still’s disease and hereditary periodic fever syndromes by Sighart, Regina (Author) , Blank, Norbert (Author) , Löhrer, Sabina (Author) , Reis, André (Author) , Hüffmeier, Ulrike (Author) ,

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Behavioral phenotype in five individuals with de novo mutations within the GRIN2B gene by Freunscht, Inga (Author) , Popp, Bernt (Author) , Blank, Rainer (Author) , Endele, Sabine (Author) , Moog, Ute (Author) , Petri, Holger (Author) , Prott, Eva-Christina (Author) , Reis, André (Author) , Rübo, Jochen (Author) , Zabel, Bernhard (Author) , Zenker, Martin (Author) , Hebebrand, Johannes (Author) , Wieczorek, Dagmar (Author) ,

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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes by Endele, Sabine (Author) , Rosenberger, Georg (Author) , Geider, Kirsten (Author) , Popp, Bernt (Author) , Tamer, Ceyhun (Author) , Stefanova, Irina (Author) , Milh, Mathieu (Author) , Kortüm, Fanny (Author) , Fritsch, Angela (Author) , Pientka, Friederike K. (Author) , Hellenbroich, Yorck (Author) , Kalscheuer, Vera M. (Author) , Kohlhase, Jürgen (Author) , Moog, Ute (Author) , Rappold, Gudrun (Author) , Rauch, Anita (Author) , Ropers, Hans-Hilger (Author) , von Spiczak, Sarah (Author) , Tönnies, Holger (Author) , Villeneuve, Nathalie (Author) , Villard, Laurent (Author) , Zabel, Bernhard (Author) , Zenker, Martin (Author) , Laube, Bodo (Author) , Reis, André (Author) , Wieczorek, Dagmar (Author) , Van Maldergem, Lionel (Author) , Kutsche, Kerstin (Author) ,

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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree by Omran, Heymut (Author) , Fernandez, Carmen (Author) , Jung, Martin (Author) , Häffner, Karsten (Author) , Fargier, Bernardo (Author) , Villaquiran, Aminta (Author) , Waldherr, Rüdiger (Author) , Gretz, Norbert (Author) , Brandis, Matthias (Author) , Rüschendorf, Franz (Author) , Reis, André (Author) , Hildebrandt, Friedhelm (Author) ,

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