Naesens, Maarten;Budde, Klemens;Hilbrands, Luuk;Oberbauer, Rainer;Bellini, Maria Irene;Glotz, Denis;Grinyó, Josep;Heemann, Uwe;Jochmans, Ina;Pengel, Liset;Reinders, Marlies;Schneeberger, Stefan;Loupy, Alexandre
Surrogate Endpoints for Late Kidney Transplantation Failure.
Transpl Int
2022
35

Al Ojaimi, Mode;Banimortada, Bashar J;Othman, Amna;Riedhammer, Korbinian M;Almannai, Mohammed;El-Hattab, Ayman W
Disorders of histone methylation: Molecular basis and clinical syndromes.
Clin Genet
2022
102
3
169-181

Reifenrath, Johannes;Seiferth, Nick;Wilhelm, Theresa;Holzmann-Littig, Christopher;Phillip, Veit;Wijnen-Meijer, Marjo
Integrated clinical case discussions - a fully student-organized peer-teaching program on internal medicine.
BMC Med Educ
2022
22
1

Würstle, Silvia;Erber, Johanna;Hanselmann, Michael;Hoffmann, Dieter;Werfel, Stanislas;Hering, Svenja;Weidlich, Simon;Schneider, Jochen;Franke, Ralf;Maier, Michael;Henkel, Andreas G;Schmid, Roland M;Protzer, Ulrike;Laxy, Michael;Spinner, Christoph D
A Telemedicine-Guided Self-Collection Approach for PCR-Based SARS-CoV-2 Testing: Comparative Study.
JMIR Form Res
2022
6
1

Günthner, Roman;Knipping, Lea;Jeruschke, Stefanie;Satanoskij, Robin;Lorenz-Depiereux, Bettina;Hemmer, Clara;Braunisch, Matthias C;Riedhammer, Korbinian M;Ćomić, Jasmina;Tönshoff, Burkhard;Tasic, Velibor;Abazi-Emini, Nora;Nushi-Stavileci, Valbona;Buiting, Karin;Gjorgjievski, Nikola;Momirovska, Ana;Patzer, Ludwig;Kirschstein, Martin;Gross, Oliver;Lungu, Adrian;Weber, Stefanie;Renders, Lutz;Heemann, Uwe;Meitinger, Thomas;Büscher, Anja K;Hoefele, Julia
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age.
Front Med (Lausanne)
2022
9

Zhang, Ling;Hauske, Sibylle;Ono, Yasuhisa;Kyaw, Moe H;Steubl, Dominik;Naito, Yusuke;Kanasaki, Keizo
Analysis of eGFR index category and annual eGFR slope association with adverse clinical outcomes using real-world Japanese data: a retrospective database study.
BMJ Open
2022
12
2

Werner, Anne;Popp, Maria;Fichtner, Falk;Holzmann-Littig, Christopher;Kranke, Peter;Steckelberg, Anke;Lühnen, Julia;Redlich, Lisa Marie;Dickel, Steffen;Grimm, Clemens;Moerer, Onnen;Nothacker, Monika;Seeber, Christian
COVID-19 Intensive Care-Evaluation of Public Information Sources and Current Standards of Care in German Intensive Care Units: A Cross Sectional Online Survey on Intensive Care Staff in Germany.
Healthcare (Basel)
2022
10
7

Breuer, Katinka;Riedhammer, Korbinian M;Müller, Nicole;Schaidinger, Birthe;Dombrowsky, Gregor;Dittrich, Sven;Zeidler, Susanne;Bauer, Ulrike M M;Westphal, Dominik S;Meitinger, Thomas;Dakal, Tikam Chand;Hitz, Marc-Phillip;Breuer, Johannes;Reutter, Heiko;Hilger, Alina C;Hoefele, Julia
Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genes.
Eur J Hum Genet
2022
30
8
946-954

Najafi, Maryam;Riedhammer, Korbinian M;Rad, Aboulfazl;Torbati, Paria Najarzadeh;Berutti, Riccardo;Schüle, Isabel;Schroda, Sophie;Meitinger, Thomas;Ćomić, Jasmina;Bojd, Simin Sadeghi;Baranzehi, Tayebeh;Shojaei, Azadeh;Azarfar, Anoush;Khazaei, Mahmood Reza;Köttgen, Anna;Backofen, Rolf;Karimiani, Ehsan Ghayoor;Hoefele, Julia;Schmidts, Miriam
High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases.
Front Pediatr
2022
10

Weng, Rosa;Nenning, Karl-Heinz;Schwarz, Michelle;Riedhammer, Korbinian M;Brunet, Theresa;Wagner, Matias;Kasprian, Gregor;Lehrner, Johann;Zimprich, Fritz;Bonelli, Silvia B;Krenn, Martin
Connectome Analysis in an Individual with SETD1B -Related Neurodevelopmental Disorder and Epilepsy.
J Dev Behav Pediatr
2022
43
6
e419-e422