Items where Author is "Schmidts, Miriam"

Article

Scherer, Nora and Faessler, Daniel and Borisov, Oleg and Cheng, Yurong and Schlosser, Pascal and Wuttke, Matthias and Haug, Stefan and Li, Yong and Telkaemper, Fabian and Patil, Suraj and Meiselbach, Heike and Wong, Casper and Berger, Urs and Sekula, Peggy and Hoppmann, Anselm and Schultheiss, Ulla T. and Mozaffari, Sahar and Xi, Yannan and Graham, Robert and Schmidts, Miriam and Koettgen, Michael and Oefner, Peter J. and Knauf, Felix and Eckardt, Kai-Uwe and Gruenert, Sarah C. and Estrada, Karol and Thiele, Ines and Hertel, Johannes and Koettgen, Anna (2025) Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits. NATURE GENETICS, 57 (1). ISSN 1061-4036, 1546-1718

Cheng, Yurong and Schlosser, Pascal and Hertel, Johannes and Sekula, Peggy and Oefner, Peter J. and Spiekerkoetter, Ute and Mielke, Johanna and Freitag, Daniel F. and Schmidts, Miriam and Kronenberg, Florian and Eckardt, Kai-Uwe and Thiele, Ines and Li, Yong and Koettgen, Anna (2021) Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism. NATURE COMMUNICATIONS, 12 (1): 964. ISSN 2041-1723,

Noethe-Menchen, Tabea and Wallmeier, Julia and Pennekamp, Petra and Hoeben, Inga M. and Olbrich, Heike and Loges, Niki T. and Raidt, Johanna and Dougherty, Gerard W. and Hjeij, Rim and Dworniczak, Bernd and Omran, Heymut and Amirav, Israel and Biebach, Luisa and Fabricius, Dorit and Griese, Matthias and Grosse-Onnebrink, Joerg and Haeffner, Karsten and Hector, Andreas and Jung, Andreas and Kaiser-Labusch, Petra and Kaiser, Thomas and Kessler, Christina and Kitz, Richard and Knowles, Michael R. and Koerner-Rettberg, Cordula and Kristoffersson, Ulf and Leigh, Margaret W. and Mertsch, Pontus and Mischo, Bernhard and Nielsen, Kim G. and Poeta, Marco and Rietschel, Ernst and Roth, Samra and Santamaria, Francesca and Schmalstieg, Christian and Schmidts, Miriam and Schwarz, Carsten and Schwerk, Nicolaus and Seithe, Horst and Tebbe, Johannes and Werner, Claudius and Zariwala, Maimoona A. (2019) Randomization of Left-Right Asymmetry and Congenital Heart Defects The Role of DNAH5 in Humans and Mice. CIRCULATION-GENOMIC AND PRECISION MEDICINE, 12 (11). ISSN 1942-325X

Olbrich, Heike and Schmidts, Miriam and Werner, Claudius and Onoufriadis, Alexandros and Loges, Niki T. and Raidt, Johanna and Banki, Nora Fanni and Shoemark, Amelia and Burgoyne, Tom and Al Turki, Saeed and Hurles, Matthew E. and Koehler, Gabriele and Schroeder, Josef and Nuernberg, Gudrun and Nuernberg, Peter and Chung, Eddie M. K. and Reinhardt, Richard and Marthin, June K. and Nielsen, Kim G. and Mitchison, Hannah M. and Omran, Heymut (2012) Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry. AMERICAN JOURNAL OF HUMAN GENETICS, 91 (4). pp. 672-684. ISSN 0002-9297

Other

Schlosser, Pascal and Scherer, Nora and Grundner-Culemann, Franziska and Monteiro-Martins, Sara and Haug, Stefan and Steinbrenner, Inga and Uluvar, Burulca and Wuttke, Matthias and Cheng, Yurong and Ekici, Arif B. and Gyimesi, Gergely and Karoly, Edward D. and Kotsis, Fruzsina and Mielke, Johanna and Gomez, Maria F. and Yu, Bing and Grams, Morgan E. and Coresh, Josef and Boerwinkle, Eric and Kottgen, Michael and Kronenberg, Florian and Meiselbach, Heike and Mohney, Robert P. and Akilesh, Shreeram and Schmidts, Miriam and Hediger, Matthias A. and Schultheiss, Ulla T. and Eckardt, Kai-Uwe and Oefner, Peter J. and Sekula, Peggy and Li, Yong and Koettgen, Anna (2023) Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. NATURE PORTFOLIO, BERLIN.