Proteomics: Progress and Promise of High-Throughput Proteomics in Chronic Kidney Disease

por Schlosser, Pascal, Grams, Morgan E., Rhee, Eugene P.
Publicado 2023

pgainsim: an R-package to assess the mode of inheritance for quantitative trait loci in GWAS

por Scherer, Nora, Sekula, Peggy, Pfaffelhuber, Peter, Schlosser, Pascal
Publicado 2021

GenToS: Use of Orthologous Gene Information to Prioritize Signals from Human GWAS

por Hoppmann, Anselm S., Schlosser, Pascal, Backofen, Rolf, Lausch, Ekkehart, Köttgen, Anna
Publicado 2016

Integrated proteomic and metabolomic modules identified as biomarkers of mortality in the Atherosclerosis Risk in Communities study and the African American Study of Kidney Disease...

por Zhou, Linda, Surapaneni, Aditya, Rhee, Eugene P., Yu, Bing, Boerwinkle, Eric, Coresh, Josef, Grams, Morgan E., Schlosser, Pascal
Publicado 2022

Epigenome-wide DNA methylation in obsessive-compulsive disorder

por Schiele, Miriam A., Lipovsek, Jan, Schlosser, Pascal, Soutschek, Michael, Schratt, Gerhard, Zaudig, Michael, Berberich, Götz, Köttgen, Anna, Domschke, Katharina
Publicado 2022

Circulating Proteins and Mortality in CKD: A Proteomics Study of the AASK and ARIC Cohorts

por Srialluri, Nityasree, Surapaneni, Aditya, Schlosser, Pascal, Chen, Teresa K., Schmidt, Insa M., Rhee, Eugene P., Coresh, Josef, Grams, Morgan E.
Publicado 2023

Integrative Network-based Analysis of Magnetic Resonance Spectroscopy and Genome Wide Expression in Glioblastoma multiforme

por Heiland, Dieter Henrik, Mader, Irina, Schlosser, Pascal, Pfeifer, Dietmar, Carro, Maria Stella, Lange, Thomas, Schwarzwald, Ralf, Vasilikos, Ioannis, Urbach, Horst, Weyerbrock, Astrid
Publicado 2016

Serum Metabolites and Kidney Outcomes: The Atherosclerosis Risk in Communities Study

por Bernard, Lauren, Zhou, Linda, Surapaneni, Aditya, Chen, Jingsha, Rebholz, Casey M., Coresh, Josef, Yu, Bing, Boerwinkle, Eric, Schlosser, Pascal, Grams, Morgan E.
Publicado 2022

A genome-wide association study identifies 41 loci associated with eicosanoid levels

por Rhee, Eugene P., Surapaneni, Aditya L., Schlosser, Pascal, Alotaibi, Mona, Yang, Yueh-ning, Coresh, Josef, Jain, Mohit, Cheng, Susan, Yu, Bing, Grams, Morgan E.
Publicado 2023

The DNA methylome in panic disorder: a case-control and longitudinal psychotherapy-epigenetic study

por Ziegler, Christiane, Grundner-Culemann, Franziska, Schiele, Miriam A., Schlosser, Pascal, Kollert, Leonie, Mahr, Marina, Gajewska, Agnieszka, Lesch, Klaus-Peter, Deckert, Jürgen, Köttgen, Anna, Domschke, Katharina
Publicado 2019

Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease

por Getwan, Maike, Hoppmann, Anselm, Schlosser, Pascal, Grand, Kelli, Song, Weiting, Diehl, Rebecca, Schroda, Sophie, Heeg, Florian, Deutsch, Konstantin, Hildebrandt, Friedhelm, Lausch, Ekkehart, Köttgen, Anna, Lienkamp, Soeren S.
Publicado 2021

Transcriptome- and proteome-wide association studies nominate determinants of kidney function and damage

por Schlosser, Pascal, Zhang, Jingning, Liu, Hongbo, Surapaneni, Aditya L., Rhee, Eugene P., Arking, Dan E., Yu, Bing, Boerwinkle, Eric, Welling, Paul A., Chatterjee, Nilanjan, Susztak, Katalin, Coresh, Josef, Grams, Morgan E.
Publicado 2023

Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism

por Cheng, Yurong, Schlosser, Pascal, Hertel, Johannes, Sekula, Peggy, Oefner, Peter J., Spiekerkoetter, Ute, Mielke, Johanna, Freitag, Daniel F., Schmidts, Miriam, Kronenberg, Florian, Eckardt, Kai-Uwe, Thiele, Ines, Li, Yong, Köttgen, Anna
Publicado 2021

Author Correction: Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism

por Cheng, Yurong, Schlosser, Pascal, Hertel, Johannes, Sekula, Peggy, Oefner, Peter J., Spiekerkoetter, Ute, Mielke, Johanna, Freitag, Daniel F., Schmidts, Miriam, Kronenberg, Florian, Eckardt, Kai-Uwe, Thiele, Ines, Li, Yong, Köttgen, Anna
Publicado 2021

In vivo kinetics of early, non-random methylome and transcriptome changes induced by DNA-hypomethylating treatment in primary AML blasts

por Greve, Gabriele, Andrieux, Geoffroy, Schlosser, Pascal, Blagitko-Dorfs, Nadja, Rehman, Usama-Ur, Ma, Tobias, Pfeifer, Dietmar, Heil, Gerhard, Neubauer, Andreas, Krauter, Jürgen, Heuser, Michael, Salih, Helmut R., Döhner, Konstanze, Döhner, Hartmut, Hackanson, Björn, Boerries, Melanie, Lübbert, Michael
Publicado 2023

38 Plasma proteomic signature of motoric cognitive risk syndrome

por Gomez, Gabriela T., Sathyan, Sanish, Chen, Jingsha, Fornage, Myriam, Schlosser, Pascal, Peng, Zhongsheng, Cordon, Jenifer, Palta, Priya, Sullivan, Kevin J., Tin, Adrienne, Windham, B. Gwen, Gottesman, Rebecca F., Coresh, Josef, Barzilai, Nir, Milman, Sofiya, Verghese, Joe, Walker, Keenan A.
Publicado 2023

Epigenome-wide association studies identify DNA methylation associated with kidney function

por Chu, Audrey Y., Tin, Adrienne, Schlosser, Pascal, Ko, Yi-An, Qiu, Chengxiang, Yao, Chen, Joehanes, Roby, Grams, Morgan E., Liang, Liming, Gluck, Caroline A., Liu, Chunyu, Coresh, Josef, Hwang, Shih-Jen, Levy, Daniel, Boerwinkle, Eric, Pankow, James S., Yang, Qiong, Fornage, Myriam, Fox, Caroline S., Susztak, Katalin, Köttgen, Anna
Publicado 2017

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

por Stanzick, Kira J., Li, Yong, Schlosser, Pascal, Gorski, Mathias, Wuttke, Matthias, Thomas, Laurent F., Rasheed, Humaira, Rowan, Bryce X., Graham, Sarah E., Vanderweff, Brett R., Patil, Snehal B., Robinson-Cohen, Cassiane, Gaziano, John M., O’Donnell, Christopher J., Willer, Cristen J., Hallan, Stein, Åsvold, Bjørn Olav, Gessner, Andre, Hung, Adriana M., Pattaro, Cristian, Köttgen, Anna, Stark, Klaus J., Heid, Iris M., Winkler, Thomas W.
Publicado 2021

Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine

por Schlosser, Pascal, Scherer, Nora, Grundner-Culemann, Franziska, Monteiro-Martins, Sara, Haug, Stefan, Steinbrenner, Inga, Uluvar, Burulça, Wuttke, Matthias, Cheng, Yurong, Ekici, Arif B., Gyimesi, Gergely, Karoly, Edward D., Kotsis, Fruzsina, Mielke, Johanna, Gomez, Maria F., Yu, Bing, Grams, Morgan E., Coresh, Josef, Boerwinkle, Eric, Köttgen, Michael, Kronenberg, Florian, Meiselbach, Heike, Mohney, Robert P., Akilesh, Shreeram, Schmidts, Miriam, Hediger, Matthias A., Schultheiss, Ulla T., Eckardt, Kai-Uwe, Oefner, Peter J., Sekula, Peggy, Li, Yong, Köttgen, Anna
Publicado 2023

Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases

por Li, Yong, Cheng, Yurong, Consolato, Francesco, Schiano, Guglielmo, Chong, Michael R., Pietzner, Maik, Nguyen, Ngoc Quynh H., Scherer, Nora, Biggs, Mary L., Kleber, Marcus E., Haug, Stefan, Göçmen, Burulça, Pigeyre, Marie, Sekula, Peggy, Steinbrenner, Inga, Schlosser, Pascal, Joseph, Christina B., Brody, Jennifer A., Grams, Morgan E., Hayward, Caroline, Schultheiss, Ulla T., Krämer, Bernhard K., Kronenberg, Florian, Peters, Annette, Seissler, Jochen, Steubl, Dominik, Then, Cornelia, Wuttke, Matthias, März, Winfried, Eckardt, Kai-Uwe, Gieger, Christian, Boerwinkle, Eric, Psaty, Bruce M., Coresh, Josef, Oefner, Peter J., Pare, Guillaume, Langenberg, Claudia, Scherberich, Jürgen E., Yu, Bing, Akilesh, Shreeram, Devuyst, Olivier, Rampoldi, Luca, Köttgen, Anna
Publicado 2022