Items where Author is "Nürnberg, Peter"

2017

Li, Man and Li, Yong and Weeks, Olivia and Mijatovic, Vladan and Teumer, Alexander and Huffman, Jennifer E. and Tromp, Gerard and Fuchsberger, Christian and Gorski, Mathias and Lyytikäinen, Leo-Pekka and Nutile, Teresa and Sedaghat, Sanaz and Sorice, Rossella and Tin, Adrienne and Yang, Qiong and Ahluwalia, Tarunveer S. and Arking, Dan E. and Bihlmeyer, Nathan A. and Böger, Carsten A. and Carroll, Robert J. and Chasman, Daniel I. and Cornelis, Marilyn C. and Dehghan, Abbas and Faul, Jessica D. and Feitosa, Mary F. and Gambaro, Giovanni and Gasparini, Paolo and Giulianini, Franco and Heid, Iris and Huang, Jinyan and Imboden, Medea and Jackson, Anne U. and Jeff, Janina and Jhun, Min A. and Katz, Ronit and Kifley, Annette and Kilpeläinen, Tuomas O. and Kumar, Ashish and Laakso, Markku and Li-Gao, Ruifang and Lohman, Kurt and Lu, Yingchang and Mägi, Reedik and Malerba, Giovanni and Mihailov, Evelin and Mohlke, Karen L. and Mook-Kanamori, Dennis O. and Robino, Antonietta and Ruderfer, Douglas and Salvi, Erika and Schick, Ursula M. and Schulz, Christina-Alexandra and Smith, Albert V. and Smith, Jennifer A. and Traglia, Michela and Yerges-Armstrong, Laura M. and Zhao, Wei and Goodarzi, Mark O. and Kraja, Aldi T. and Liu, Chunyu and Wessel, Jennifer and Charge Blood Pressure Working Group, and Boerwinkle, Eric and Borecki, Ingrid B. and Bork-Jensen, Jette and Bottinger, Erwin P. and Braga, Daniele and Brandslund, Ivan and Brody, Jennifer A. and Campbell, Archie and Carey, David J. and Christensen, Cramer and Coresh, Josef and Crook, Errol and Curhan, Gary C. and Cusi, Daniele and de Boer, Ian H. and de Vries, Aiko P. J. and Denny, Joshua C. and Devuyst, Olivier and Dreisbach, Albert W. and Endlich, Karlhans and Esko, Tõnu and Franco, Oscar H. and Fulop, Tibor and Gerhard, Glenn S. and Glümer, Charlotte and Gottesman, Omri and Grarup, Niels and Gudnason, Vilmundur and Hansen, Torben and Harris, Tamara B. and Hayward, Caroline and Hocking, Lynne and Hofman, Albert and Hu, Frank B. and Husemoen, Lise Lotte N. and Jackson, Rebecca D. and Jørgensen, Torben and Jørgensen, Marit E. and Kähönen, Mika and Kardia, Sharon L. R. and König, Wolfgang and Kooperberg, Charles and Kriebel, Jennifer and Launer, Lenore J. and Lauritzen, Torsten and Lehtimäki, Terho and Levy, Daniel and Linksted, Pamela and Linneberg, Allan and Liu, Yongmei and Loos, Ruth J. F. and Lupo, Antonio and Meisinger, Christine and Melander, Olle and Metspalu, Andres and Mitchell, Paul and Nauck, Matthias and Nürnberg, Peter and Orho-Melander, Marju and Parsa, Afshin and Pedersen, Oluf and Peters, Annette and Peters, Ulrike and Polasek, Ozren and Porteous, David and Probst-Hensch, Nicole M. and Psaty, Bruce M. and Qi, Lu and Raitakari, Olli T. and Reiner, Alex P. and Rettig, Rainer and Ridker, Paul M. and Rivadeneira, Fernando and Rossouw, Jacques E. and Schmidt, Frank and Siscovick, David and Soranzo, Nicole and Strauch, Konstantin and Toniolo, Daniela and Turner, Stephen T. and Uitterlinden, André G. and Ulivi, Sheila and Velayutham, Dinesh and Völker, Uwe and Völzke, Henry and Waldenberger, Melanie and Wang, Jie Jin and Weir, David R. and Witte, Daniel and Kuivaniemi, Helena and Fox, Caroline S. and Franceschini, Nora and Goessling, Wolfram and Köttgen, Anna and Chu, Audrey Y.. (2017) SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function. Clinical journal of the American Society of Nephrology, 28 (3). pp. 981-994.

2014

Smolonska, Joanna and Koppelman, Gerard H. and Wijmenga, Cisca and Vonk, Judith M. and Zanen, Pieter and Bruinenberg, Marcel and Curjuric, Ivan and Imboden, Medea and Thun, Gian-Andri and Franke, Lude and Probst-Hensch, Nicole M. and Nürnberg, Peter and Riemersma, Roland A. and van Schayck, Constant P. and Loth, Daan W. and Brusselle, Guy G. and Stricker, Bruno H. and Hofman, Albert and Uitterlinden, André G. and Lahousse, Lies and London, Stephanie J. and Loehr, Laura R. and Manichaikul, Ani and Barr, R. Graham and Donohue, Kathleen M. and Rich, Stephen S. and Pare, Peter and Bossé, Yohan and Hao, Ke and van den Berge, Maarten and Groen, Harry J. M. and Lammers, Jan-Willem J. and Mali, Willem and Boezen, H. Marike and Postma, Dirkje S.. (2014) Common genes underlying asthma and COPD? : Genome-wide analysis on the Dutch hypothesis. The European respiratory journal, 44 (4). pp. 860-872.

2010

Gailus, Susann and Suormala, Terttu and Malerczyk-Aktas, Ayse Gül and Toliat, Mohammad R. and Wittkampf, Tanja and Stucki, Martin and Nürnberg, Peter and Fowler, Brian and Hennermann, Julia B. and Rutsch, Frank. (2010) A novel mutation in LMBRD1 causes the cblF defect of vitamin B(12) metabolism in a Turkish patient. Journal of Inherited Metabolic Disease, Vol. 33, no. 1. pp. 17-24.

Gailus, Susann and Höhne, Wolfgang and Gasnier, Bruno and Nürnberg, Peter and Fowler, Brian and Rutsch, Frank. (2010) Insights into lysosomal cobalamin trafficking : lessons learned from cblF disease. Journal of molecular medicine, Vol. 88, no. 5. pp. 459-466.

2009

Rutsch, Frank and Gailus, Susann and Miousse, Isabelle R. and Suormala, Terttu and Sagné, Corinne and Toliat, Mohammad Reza and Nürnberg, Gudrun and Wittkampf, Tanja and Buers, Insa and Sharifi, Azita and Stucki, Martin and Becker, Christian and Baumgartner, Matthias and Robenek, Horst and Marquardt, Thorsten and Höhne, Wolfgang and Gasnier, Bruno and Rosenblatt, David S. and Fowler, Brian and Nürnberg, Peter. (2009) Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. Nature genetics, Vol. 41, H. 2. pp. 234-239.