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Nature genetics, ISSN 1546-1718, 2016, Volume 48, Issue 10, pp. 1279 - 1283
We describe a reference panel of 64,976 human haplotypes at 39,235,157 SNPs constructed using whole-genome sequence data from 20 studies of predominantly... 
POPULATION | RARE VARIANTS | SEQUENCE | GENOME-WIDE ASSOCIATION | Studies | Datasets | Haplotypes | Consortia | Accuracy | Genealogy | Researchers | Genomics | Collaboration | Genomes | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Cell stem cell, ISSN 1934-5909, 2017, Volume 21, Issue 5, pp. 569 - 573
Stem cell-based therapies for Parkinson’s disease are moving into a new and exciting era, with several groups pursuing clinical trials with pluripotent stem... 
THERAPIES | MODEL | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
by Nikpay, Majid and Goel, Anuj and Won, Hong-Hee and Hall, Leanne M and Willenborg, Christina and Kanoni, Stavroula and Saleheen, Danish and Kyriakou, Theodosios and Nelson, Christopher P and CHopewell, Jemma and Webb, Thomas R and Zeng, Lingyao and Dehghan, Abbas and Alver, Maris and MArmasu, Sebastian and Auro, Kirsi and Bjonnes, Andrew and Chasman, Daniel I and Chen, Shufeng and Ford, Ian and Franceschini, Nora and Gieger, Christian and Grace, Christopher and Gustafsson, Stefan and Huang, Jie and Hwang, Shih-Jen and Kim, Yun Kyoung and Kleber, Marcus E and Lau, King Wai and Lu, Xiangfeng and Lu, Yingchang and Lyytikäinen, Leo-Pekka and Mihailov, Evelin and Morrison, Alanna C and Pervjakova, Natalia and Qu, Liming and Rose, Lynda M and Salfati, Elias and Saxena, Richa and Scholz, Markus and Smith, Albert V and Tikkanen, Emmi and Uitterlinden, Andre and Yang, Xueli and Zhang, Weihua and Zhao, Wei and De Andrade, Mariza and De Vries, Paul S and Van Zuydam, Natalie R and Anand, Sonia S and Bertram, Lars and Beutner, Frank and Dedoussis, George and Frossard, Philippe and Gauguier, Dominique and Goodall, Alison H and Gottesman, Omri and Haber, Marc and Han, Bok-Ghee and Huang, Jianfeng and Jalilzadeh, Shapour and Kessler, Thorsten and König, Inke R and Lannfelt, Lars and Lieb, Wolfgang and Lind, Lars and MLindgren, Cecilia and Lokki, Marja-Liisa and Magnusson, Patrik K and Mallick, Nadeem H and Mehra, Narinder and Meitinger, Thomas and Memon, Fazal-Uur-Rehman and Morris, Andrew P and Nieminen, Markku S and Pedersen, Nancy L and Peters, Annette and Rallidis, Loukianos S and Rasheed, Asif and Samuel, Maria and Shah, Svati H and Sinisalo, Juha and EStirrups, Kathleen and Trompet, Stella and Wang, Laiyuan and Zaman, Khan S and Ardissino, Diego and Boerwinkle, Eric and Borecki, Ingrid B and Bottinger, Erwin P and Buring, Julie E and Chambers, John C and Collins, Rory and Cupples, Ladrienne and Danesh, John and Demuth, Ilja and Elosua, Roberto and Epstein, Stephen E and Esko, Tõnu and Feitosa, Mary F and ... and the CARDIoGRAMplusC4D Consortium and CARDIoGRAMplusC4D Consortium
Nature genetics, ISSN 1546-1718, 2015, Volume 47, Issue 10, pp. 1121 - 1130
Journal Article
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Bramon, Elvira and Corvin, Aiden P and O'Donovan, Michael C and Stefansson, Kari and Scolnick, Edward and Purcell, Shaun and McCarroll, Steven A and Sklar, Pamela and Hultman, Christina M and Sullivan, Patrick F and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 10, pp. 1150 - 1159
Journal Article
Journal Article
by Nik-Zainal, Serena and Davies, Helen and Staaf, Johan and Ramakrishna, Manasa and Glodzik, Dominik and Zou, Xueqing and Martincorena, Inigo and Alexandrov, Ludmil B and Martin, Sancha and Wedge, David C and Van Loo, Peter and Ju, Young Seok and Smid, Marcel and Brinkman, Arie B and Morganella, Sandro and Aure, Miriam R and Lingjærde, Ole Christian and Langerød, Anita and Ringnér, Markus and Ahn, Sung-Min and Boyault, Sandrine and Brock, Jane E and Broeks, Annegien and Butler, Adam and Desmedt, Christine and Dirix, Luc and Dronov, Serge and Fatima, Aquila and Foekens, John A and Gerstung, Moritz and Hooijer, Gerrit K. J and Jang, Se Jin and Jones, David R and Kim, Hyung-Yong and King, Tari A and Krishnamurthy, Savitri and Lee, Hee Jin and Lee, Jeong-Yeon and Li, Yilong and McLaren, Stuart and Menzies, Andrew and Mustonen, Ville and O’Meara, Sarah and Pauporté, Iris and Pivot, Xavier and Purdie, Colin A and Raine, Keiran and Ramakrishnan, Kamna and Rodríguez-González, F. Germán and Romieu, Gilles and Sieuwerts, Anieta M and Simpson, Peter T and Shepherd, Rebecca and Stebbings, Lucy and Stefansson, Olafur A and Teague, Jon and Tommasi, Stefania and Treilleux, Isabelle and Van den Eynden, Gert G and Vermeulen, Peter and Vincent-Salomon, Anne and Yates, Lucy and Caldas, Carlos and Veer, Laura van’t and Tutt, Andrew and Knappskog, Stian and Tan, Benita Kiat Tee and Jonkers, Jos and Borg, Åke and Ueno, Naoto T and Sotiriou, Christos and Viari, Alain and Futreal, P. Andrew and Campbell, Peter J and Span, Paul N and Van Laere, Steven and Lakhani, Sunil R and Eyfjord, Jorunn E and Thompson, Alastair M and Birney, Ewan and Stunnenberg, Hendrik G and van de Vijver, Marc J and Martens, John W. M and Børresen-Dale, Anne-Lise and Richardson, Andrea L and Kong, Gu and Thomas, Gilles and Stratton, Michael R and Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
Nature (London), ISSN 1476-4687, 2016, Volume 534, Issue 7605, pp. 47 - 54
Journal Article
Cell Death and Disease, ISSN 2041-4889, 2013, Volume 4, Issue 10, pp. e881 - e881
  The low-molecular-weight compound APR-246 (PRIMA-1MET ) restores wild-type conformation and function to mutant p53, and triggers apoptosis in tumor cells. We... 
Mutant p53 | APR-246 | PRIMA-1MET | ROS | Thioredoxin reductase 1 | Farmakologi och toxikologi | Medicin och hälsovetenskap | Cell- och molekylärbiologi | Medicinska och farmaceutiska grundvetenskaper
Journal Article