Quarta, Carmelo;Clemmensen, Christoffer;Zhu, Zhimeng;Yang, Bin;Joseph, Sini S;Lutter, Dominik;Yi, Chun-Xia;Graf, Elisabeth;García-Cáceres, Cristina;Legutko, Beata;Fischer, Katrin;Brommage, Robert;Zizzari, Philippe;Franklin, Bernardo S;Krueger, Martin;Koch, Marco;Vettorazzi, Sabine;Li, Pengyun;Hofmann, Susanna M;Bakhti, Mostafa;Bastidas-Ponce, Aimée;Lickert, Heiko;Strom, Tim M;Gailus-Durner, Valerie;Bechmann, Ingo;Perez-Tilve, Diego;Tuckermann, Jan;Hrab? de Angelis, Martin;Sandoval, Darleen;Cota, Daniela;Latz, Eicke;Seeley, Randy J;Müller, Timo D;DiMarchi, Richard D;Finan, Brian;Tschöp, Matthias H.Molecular Integration of Incretin and Glucocorticoid Action Reverses Immunometabolic Dysfunction and Obesity..Cell Metab.2017.26.4.620-632.e6

Zech, Michael;Jech, Robert;Havránková, Petra;Fe?íková, Anna;Berutti, Riccardo;Urgo?ík, Du?an;Kemlink, David;Strom, Tim M;Roth, Jan;R??i?ka, Ev?en;Winkelmann, Juliane.KMT2B rare missense variants in generalized dystonia..Mov Disord.2017.32.7.1087-1091

Ullah, Asmat;Umair, Muhammad;Yousaf, Maryam;Khan, Sher Alam;Nazim-Ud-Din, Muhammad;Shah, Khadim;Ahmad, Farooq;Azeem, Zahid;Ali, Ghazanfar;Alhaddad, Bader;Rafique, Afzal;Jan, Abid;Haack, Tobias B;Strom, Tim M;Meitinger, Thomas;Ghous, Tahseen;Ahmad, Wasim.Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families..Mol Vis.2017.23.482-494

Biagosch, Caroline;Ediga, Raga Deepthi;Hensler, Svenja-Viola;Faerberboeck, Michael;Kuehn, Ralf;Wurst, Wolfgang;Meitinger, Thomas;Kölker, Stefan;Sauer, Sven;Prokisch, Holger.Elevated glutaric acid levels in Dhtkd1-/Gcdh- double knockout mice challenge our current understanding of lysine metabolism..Biochim Biophys Acta.2017.1863.9.2220-2228

Macé, Aurélien;Tuke, Marcus A;Deelen, Patrick;Kristiansson, Kati;Mattsson, Hannele;Nõukas, Margit;Sapkota, Yadav;Schick, Ursula;Porcu, Eleonora;Rüeger, Sina;McDaid, Aaron F;Porteous, David;Winkler, Thomas W;Salvi, Erika;Shrine, Nick;Liu, Xueping;Ang, Wei Q;Zhang, Weihua;Feitosa, Mary F;Venturini, Cristina;van der Most, Peter J;Rosengren, Anders;Wood, Andrew R;Beaumont, Robin N;Jones, Samuel E;Ruth, Katherine S;Yaghootkar, Hanieh;Tyrrell, Jessica;Havulinna, Aki S;Boers, Harmen;Mägi, Reedik;Kriebel, Jennifer;Müller-Nurasyid, Martina;Perola, Markus;Nieminen, Markku;Lokki, Marja-Liisa;Kähönen, Mika;Viikari, Jorma S;Geller, Frank;Lahti, Jari;Palotie, Aarno;Koponen, Päivikki;Lundqvist, Annamari;Rissanen, Harri;Bottinger, Erwin P;Afaq, Saima;Wojczynski, Mary K;Lenzini, Petra;Nolte, Ilja M;Sparsø, Thomas;Schupf, Nicole;Christensen, Kaare;Perls, Thomas T;Newman, Anne B;Werge, Thomas;Snieder, Harold;Spector, Timothy D;Chambers, John C;Koskinen, Seppo;Melbye, Mads;Raitakari, Olli T;Lehtimäki, Terho;Tobin, Martin D;Wain, Louise V;Sinisalo, Juha;Peters, Annette;Meitinger, Thomas;Martin, Nicholas G;Wray, Naomi R;Montgomery, Grant W;Medland, Sarah E;Swertz, Morris A;Vartiainen, Erkki;Borodulin, Katja;Männistö, Satu;Murray, Anna;Bochud, Murielle;Jacquemont, Sébastien;Rivadeneira, Fernando;Hansen, Thomas F;Oldehinkel, Albertine J;Mangino, Massimo;Province, Michael A;Deloukas, Panos;Kooner, Jaspal S;Freathy, Rachel M;Pennell, Craig;Feenstra, Bjarke;Strachan, David P;Lettre, Guillaume;Hirschhorn, Joel;Cusi, Daniele;Heid, Iris M;Hayward, Caroline;Männik, Katrin;Beckmann, Jacques S;Loos, Ruth J F;Nyholt, Dale R;Metspalu, Andres;Eriksson, Johan G;Weedon, Michael N;Salomaa, Veikko;Franke, Lude;Reymond, Alexandre;Frayling, Timothy M;Kutalik, Zoltán.CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits..Nat Commun.2017.8.1.744

Kamme, Christina;Mayer, Anja Kathrin;Strom, Tim M;Andréasson, Sten;Weisschuh, Nicole.Genotype and Phenotype in an unusual form of Laurence-Moon-Bardet-Biedl syndrome..Acta Ophthalmol.2017.95.3.e250-e252

Wambach, Jennifer A;Stettner, Georg M;Haack, Tobias B;Writzl, Karin;?kofljanec, Andreja;Maver, Ale?;Munell, Francina;Ossowski, Stephan;Bosio, Mattia;Wegner, Daniel J;Shinawi, Marwan;Baldridge, Dustin;Alhaddad, Bader;Strom, Tim M;Grange, Dorothy K;Wilichowski, Ekkehard;Troxell, Robin;Collins, James;Warner, Barbara B;Schmidt, Robert E;Pestronk, Alan;Cole, F Sessions;Steinfeld, Robert.Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN)..Hum Mutat.2017.38.11.1477-1484

Molnos, Sophie;Baumbach, Clemens;Wahl, Simone;Müller-Nurasyid, Martina;Strauch, Konstantin;Wang-Sattler, Rui;Waldenberger, Melanie;Meitinger, Thomas;Adamski, Jerzy;Kastenmüller, Gabi;Suhre, Karsten;Peters, Annette;Grallert, Harald;Theis, Fabian J;Gieger, Christian.pulver: an R package for parallel ultra-rapid p-value computation for linear regression interaction terms..BMC Bioinformatics.2017.18.1.429

Martin, Sonja;Chamberlin, Adam;Shinde, Deepali N;Hempel, Maja;Strom, Tim M;Schreiber, Allison;Johannsen, Jessika;Ousager, Lilian Bomme;Larsen, Martin J;Hansen, Lars Kjaersgaard;Fatemi, Ali;Cohen, Julie S;Lemke, Johannes;Sørensen, Kristina P;Helbig, Katherine L;Lessel, Davor;Abou Jamra, Rami.De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities..Am J Hum Genet.2017.101.6.1013-1020

Zhao, Feng;Durner, Jörg;Winkler, J Barbro;Traidl-Hoffmann, Claudia;Strom, Tim-Matthias;Ernst, Dieter;Frank, Ulrike.Pollen of common ragweed (Ambrosia artemisiifolia L.): Illumina-based de novo sequencing and differential transcript expression upon elevated NO/O..Environ Pollut.2017.224.503-514