Indelicato, Elisabetta;Boesch, Sylvia;Havrankova, Petra;Příhodová, Iva;Winkelmann, Juliane;Jech, Robert;Zech, Michael
SOXopathies and dystonia: Consolidation of a recurrent association.
Parkinsonism Relat Disord
2024
119

van Rosendael, Sophie E;van den Hoogen, Inge J;Lin, Fay Y;Andreini, Daniele;Al-Mallah, Mouaz H;Budoff, Matthew J;Cademartiri, Filippo;Chinnaiyan, Kavitha;Choi, Jung Hyun;Conte, Edoardo;Marques, Hugo;de Araújo Gonçalves, Pedro;Gottlieb, Ilan;Hadamitzky, Martin;Leipsic, Jonathon A;Maffei, Erica;Pontone, Gianluca;Raff, Gilbert L;Shin, Sanghoon;Kim, Yong-Jin;Lee, Byoung Kwon;Chun, Eun Ju;Sung, Ji Min;Lee, Sang-Eun;Virmani, Renu;Samady, Habib;Stone, Peter H;Min, James K;Narula, Jagat;Shaw, Leslee J;Chang, Hyuk-Jae;van Rosendael, Alexander R;Bax, Jeroen J
Clinical and Coronary Plaque Predictors of Atherosclerotic Nonresponse to Statin Therapy.
JACC Cardiovasc Imaging
2023
16
4
495-504

Steinacker, Jürgen M;van Mechelen, Willem;Bloch, Wilhelm;Börjesson, Mats;Casasco, Maurizio;Wolfarth, Bernd;Knoke, Carolin;Papadopoulou, Theodora;Wendt, Janine;Al Tunaiji, Hashel;Andresen, Dietrich;Andrieieva, Olena;Bachl, Norbert;Badtieva, Victoriya;Beucher, Friedhelm J;Blauwet, Cheri A;Casajus Mallen, Jose-Antonio;Chang, Ju-Ho;Clénin, German;Constantini, Naama;Constantinou, Demitri;Di Luigi, Luigi;Declercq, Lukas;Doutreleau, Stephane;Drozdovska, Svitlana;Duclos, Martine;Ermolao, Andrea;Fischbach, Thomas;Fischer, Anastasia N;Fossati, Chiara;Franchella, Jeorge;Fulcher, Mark;Galle, Jan C;Gerloff, Christian;Georgiades, Evelina;Gojanovic, Boris;González Gross, Marcela;Grote, Andy;Halle, Martin;Hauner, Hans;Herring, Matthew Payton;Hiura, Mikio;Holze, Kerstin;Huber, Gerhard;Hughes, David;Hutchinson, Mark R;Ionescu, Anca;Janse van Rensburg, Dina Christina;Jegier, Anna;Jones, Natasha;Kappert-Gonther, Kirsten;Kellerer, Monika;Kimura, Yutaka;Kiopa, Agrita;Kladny, Bernd;Koch, Gerhard;Kolle, Elin;Kolt, Greg;Koutedakis, Yiannis;Kress, Stephan;Kriemler, Susi;Kröger, Jens;Kuhn, Christian;Laszlo, Roman;Lehnert, Ralph;Lhuissier, François J;Lüdtke, Kerstin;Makita, Shigeru;Manonelles Marqueta, Pedro;März, Winfried;Micallef-Stafrace, Kirill;Miller, Mike;Moore, Melita;Müller, Erich;Neunhäuserer, Daniel;Onur, I Renay;Ööpik, Vahur;Perl, Malgorzata;Philippou, Anastassios;Predel, Hans-Georg;Racinais, Sebastien;Raslanas, Algirdas;Reer, Ruediger;Reinhardt, Klaus;Reinsberger, Claus;Rozenstoka, Sandra;Sallis, Robert;Sardinha, Luis B;Scherer, Martin;Schipperijn, Jasper;Seil, Romain;Tan, Benedict;Schmidt-Trucksäss, Arno;Schumacher, Nils;Schwaab, Bernhard;Schwirtz, Ansgar;Suzuki, Masato;Swart, Jeroen;Tiesler, Ralph;Tippelt, Ulf;Tillet, Eleanor;Thornton, Jane;Ulkar, Bulent;Unt, Eve;Verhagen, Evert;Weikert, Thomas;Vettor, Roberto;Zeng, Sheng;Budgett, Richard;Engebretsen, Lars;Erdener, Ugur;Pigozzi, Fabio;Pitsiladis, Yannis P
Global Alliance for the Promotion of Physical Activity: the Hamburg Declaration.
BMJ Open Sport Exerc Med
2023
9
3

Marx, Nikolaus;Federici, Massimo;Schütt, Katharina;Müller-Wieland, Dirk;Ajjan, Ramzi A;Antunes, Manuel J;Christodorescu, Ruxandra M;Crawford, Carolyn;Di Angelantonio, Emanuele;Eliasson, Björn;Espinola-Klein, Christine;Fauchier, Laurent;Halle, Martin;Herrington, William G;Kautzky-Willer, Alexandra;Lambrinou, Ekaterini;Lesiak, Maciej;Lettino, Maddalena;McGuire, Darren K;Mullens, Wilfried;Rocca, Bianca;Sattar, Naveed
2023 ESC Guidelines for the management of cardiovascular disease in patients with diabetes.
Eur Heart J
2023
44
39
4043-4140

Silvaieh, Sara;König, Theresa;Wurm, Raphael;Parvizi, Tandis;Berger-Sieczkowski, Evelyn;Goeschl, Stella;Hotzy, Christoph;Wagner, Matias;Berutti, Riccardo;Sammler, Esther;Stögmann, Elisabeth;Zimprich, Alexander
Correction: Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes.
Hum Genomics
2023
17
1

Deltas, Constantinos;Papagregoriou, Gregory;Louka, Stavroula F;Malatras, Apostolos;Flinter, Frances;Gale, Daniel P;Gear, Susie;Gross, Oliver;Hoefele, Julia;Lennon, Rachel;Miner, Jeffrey H;Renieri, Alessandra;Savige, Judy;Turner, A Neil
Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice.
Genes (Basel)
2023
14
9

Smirnov, Dmitrii;Konstantinovskiy, Nikita;Prokisch, Holger
Integrative omics approaches to advance rare disease diagnostics.
J Inherit Metab Dis
2023
46
5
824-838

Riedhammer, Korbinian;Thanh-Minh Nguyen, TM;Kosukcu, Can;Calzada-Wack, Julia;Li, Yong;Saygili, Seha;Kim, Gwang-Jin;Caliskan, Salim;Koettgen, Anna;Arnold, Sebastian;Ozaltin, Fatih;Schmidts, Miriam;Hoefele, Julia
FOXD2 DYSFUNCTION IS IMPLICATED IN SYNDROMIC CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT (CAKUT)
Pediatr Nephrol
2023
38 Suppl 2
S128-S129

Kaiyrzhanov, Rauan;Rad, Aboulfazl;Lin, Sheng-Jia;Bertoli-Avella, Aida;Kallemeijn, Wouter W;Godwin, Annie;Zaki, Maha S;Huang, Kevin;Lau, Tracy;Petree, Cassidy;Efthymiou, Stephanie;Karimiani, Ehsan Ghayoor;Hempel, Maja;Normand, Elizabeth A;Rudnik-Schöneborn, Sabine;Schatz, Ulrich A;Baggelaar, Marc P;Ilyas, Muhammad;Sultan, Tipu;Alvi, Javeria Raza;Ganieva, Manizha;Fowler, Ben;Aanicai, Ruxandra;Tayfun, Gulsen Akay;Al Saman, Abdulaziz;Alswaid, Abdulrahman;Amiri, Nafise;Asilova, Nilufar;Shotelersuk, Vorasuk;Yeetong, Patra;Azam, Matloob;Babaei, Meisam;Monajemi, Gholamreza Bahrami;Mohammadi, Pouria;Samie, Saeed;Banu, Selina Husna;Pinto Basto, Jorge;Kortüm, Fanny;Bauer, Mislen;Bauer, Peter;Beetz, Christian;Garshasbi, Masoud;Issa, Awatif Hameed;Eyaid, Wafaa;Ahmed, Hind;Hashemi, Narges;Hassanpour, Kazem;Herman, Isabella;Ibrohimov, Sherozjon;Abdul-Majeed, Ban A;Imdad, Maria;Isrofilov, Maksudjon;Kaiyal, Qassem;Khan, Suliman;Kirmse, Brian;Koster, Janet;Lourenço, Charles Marques;Mitani, Tadahiro;Moldovan, Oana;Murphy, David;Najafi, Maryam;Pehlivan, Davut;Rocha, Maria Eugenia;Salpietro, Vincenzo;Schmidts, Miriam;Shalata, Adel;Mahroum, Mohammad;Talbeya, Jawabreh Kassem;Taylor, Robert W;Vazquez, Dayana;Vetro, Annalisa;Waterham, Hans R;Zaman, Mashaya;Schrader, Tina A;Chung, Wendy K;Guerrini, Renzo;Lupski, James R;Gleeson, Joseph;Suri, Mohnish;Jamshidi, Yalda;Bhatia, Kailash P;Vona, Barbara;Schrader, Michael;Severino, Mariasavina;Guille, Matthew;Tate, Edward W;Varshney, Gaurav K;Houlden, Henry;Maroofian, Reza
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.
Brain
2024
147
4
1436-1456

Indelicato, Elisabetta;Boesch, Sylvia;Mencacci, Niccolo' E;Ghezzi, Daniele;Prokisch, Holger;Winkelmann, Juliane;Zech, Michael
Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine.
Mov Disord
2024
39
1
29-35