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1
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma
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Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma

Paul A. Northcott Yukiko Nakahara; Xiaochong Wu; Lars Freuk; David W Ellison; Sid Croul; Stephen Mack; Paul N Kongkham; John Peacock; Adrian Dubuc; Young-Shin Ra; Karen Zilberberg; Jessica Mcleod; Stephen W Scherer; J. Sunil Rao; Charles G Eberhart; Wiesia Grajkowska; Yancey Gillespie; Boleslaw Lach; Richard Grundy; Ian F Pollack; Ronald L Hamilton; Timothy Van Meter; Carlos Gilberto Carlotti Júnior; Frederick Boop; Darrell Bigner; Richard J Gilbertson; James T Rutka; Michael D Taylor

Nature Genetics New York v. 41, n. 4, p. 465-472, 2009

New York 2009

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1765088 )(Acessar)

2
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma
Material Type:
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Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma

Paul A. Northcott Yukiko Nakahara; Xiaochong Wu; Lars Freuk; David W Ellison; Sid Croul; Stephen Mack; Paul N Kongkham; John Peacock; Adrian Dubuc; Young-Shin Ra; Karen Zilberberg; Jessica Mcleod; Stephen W Scherer; J. Sunil Rao; Charles G Eberhart; Wiesia Grajkowska; Yancey Gillespie; Boleslaw Lach; Richard Grundy; Ian F Pollack; Ronald L Hamilton; Timothy Van Meter; Carlos Gilberto Carlotti Júnior; Frederick Boop; Darrell Bigner; Richard J Gilbertson; James T Rutka; Michael D Taylor

Nature Genetics New York v. 41, n. 4, p. 465-472, 2009

New York 2009

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1765088 )(Acessar)

3
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Ingrid E. Christophersen Michiel Rienstra; Carolina Roselli; Xiaoyan Yin; Bastiaan Geelhoed; John Barnard; Honghuang Lin; Dan E Arking; Albert V Smith; Christine M Albert; Mark Chaffin; Nathan R Tucker; Molong Li; Derek Klarin; Nathan A Bihlmeyer; Siew-Kee Low; Peter E Weeke; Martina Müller Nurasyid; J. Gustav Smith; Jennifer A Brody; Maartje N Niemeijer; Marcus Dörr; Stella Trompet; Jennifer Huffman; Stefan Gustafsson; Claudia Schurmann; Marcus E Kleber; Leo-Pekka Lyytikäinen; Ilkka Seppälä; Rainer Malik; Andrea R. V Horimoto; Marco Perez; Juha Sinisalo; Stefanie Aeschbacher; Sébastien Theriault; Jie Yao; Farid Radmanesh; Alexander Teumer; Seung Hoan Choi; Lu-Chen Weng; Sebastian Clauss; Rajat Deo; Daniel J Rader; Svati H Shah; Albert Sun; Jemma C Hopewell; Stephanie Debette; Ganesh Chauhan; Qiong Yang; Bradford B Worral; Guillaume Paré; Yoichiro Kamatani; Yanick P Hagemeijer; Niek Verweij; Joylene E Siland; Michiaki Kubo; Jonathan D Smith; David R. Van Wagoner; Joshua C Bis; Siegfried Perz; Bruce M Psaty; Paul M Ridker; Jared W Magnani; Tamara B Harris; Lenore J Launer; M. Benjamin Shoemaker; Sandosh Padmanabhan; Jeffrey Haessler; Traci M Bartz; Melanie Waldenberger; Peter Lichtner; José Eduardo Krieger; Mika Kähönen; Lorenz Risch; Alfredo José Mansur; Annette Peters; Blair H Smith; Lars Lind; Stuart A Scott; Yingchang Lu; Erwin B Bottinger; Jussi Hernesniemi; Cecilia M Lindgren; Jorge A Wong; Jie Huang; Markku Eskola; Andrew P Morris; Ian Ford; Alex P Reiner; Graciela Delgado; Lin Y Yen; Yii-Der Ida Chen; Roopinder Sandhu; Man Li; Eric Boerwinkle; Lewin Eisele; Lars Lannfelt; Natalia Rost; Christopher D Anderson; Kent D Taylor; Archie Campbell; Patrick K Magnusson; David Porteous; Lynne J Hoking; Efthymia Vlachopoulou; Nancy L Pedersen; Kjell Nikus; Marju Orho Melander; Anders Hamsten; Jan Heeringa; Joshua C Denny; Jennifer Kriebel; Dawood Darbar; Christopher Newton Cheh Shaffer,Christian; Peter W Macfarlane; Stefanie Heilmann Heimbach; Peter Almgren; Paul L Huang; Nona Sotoodehnia; Elsayed Z Soliman; Andre G Uitterlinden; Albert Hofman; Oscar H Franco; Uwe Völker; Karl-Heinz Jöckel Sinner,Moritz F; Henry J Lin; Xiuqing Guo; Martin Dichgans; Erik Ingelsson; Charles Kooperberg; Olle Melander; Ruth J. F Loos; Jari Laurikka; David Conen; Jonathan Rosand; Pim van der Harst; Marja-Liisa Lokki; Sekar Kathiresan; Alexandre Pereira; J. Wouter Jukema; Caroline Hayward; Jerome I Rotter; Winfried März; Terho Lehtimäki; Bruno H Stricker; Mina K Chung; Stephan B Felix; Vilmundur Gudnason; Alvaro Alonso; Dan M Roden; Stefan Kääb; Daniel I Chasman; Susan R Heckbert; Emelia J Benjamin; Toshihiro Tanaka; Kathryn L Lunetta; Steven A Lubitz; Patrick T Ellinor

Nature Genetics New York v. 49, n. 6, p. 946-952, 2017

New York 2017

Item não circula. Consulte sua biblioteca.(Acessar)

4
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
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Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

Pfeifer, Susanne P ; Hansen, Ruth M S ; Olesen, Inge A ; Meyts, Ewa Rajpert-De ; Wilkie, Andrew O M ; Goriely, Anne ; McGowan, Simon J ; Taylor, Indira B ; McVean, Gilean A T ; Jacobsen, Grete Krag

Nature genetics, 2009-11, Vol.41 (11), p.1247-1252 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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5
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation
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Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

Burmeister, Margit ; Novak, Jakub ; Liang, Mei-Ying ; Basu, Sharmila ; Ploder, Lynda ; Hawes, Norman L ; Vidgen, Danka ; Hoover, Frank ; Goldman, Daniel ; Kalnins, Vitauts I ; Roderick, Thomas H ; Taylor, Benjamin A ; Hankin, Mark H ; Mclnnes, Roderick R

Nature genetics, 1996-04, Vol.12 (4), p.376-384 [Periódico revisado por pares]

London: Nature Publishing Group

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6
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Patsopoulos, Nikolaos A ; Xifara, Dionysia K ; Davis, Mary F ; Kemppinen, Anu ; Cotsapas, Chris ; Booth, David ; Goris, An ; Martin, Claes ; D'Alfonso, Sandra ; Martinelli-Boneschi, Filippo ; Harbo, Hanne F ; Hillert, Jan ; Olsson, Tomas ; Ban, Maria ; Oksenberg, Jorge R ; Hintzen, Rogier ; Barcellos, Lisa F ; Alfredsson, Lars ; Andrews, Robert ; Baker, Amie ; Band, Gavin ; Baranzini, Sergio E ; Barizzone, Nadia ; Bernardinelli, Luisa ; Blackburn, Hannah ; Brambilla, Paola ; Brochet, Bruno ; Brundin, Lou ; Butzkueven, Helmut ; Caillier, Stacy J ; Cavalla, Paola ; Celius, Elisabeth G ; Cosemans, Leentje ; Cree, Bruce A C ; Delgado, Silvia R ; Deloukas, Panos ; di Sapio, Alessia ; Duddy, Martin ; Elovaara, Irina ; Evangelou, Nikos ; Field, Judith ; Franke, Andre ; Freeman, Colin ; Galimberti, Daniela ; Graetz, Christiane ; Graham, Andrew ; Guaschino, Clara ; Hakonarson, Hakon ; Halfpenny, Christopher ; Harrower, Timothy ; Hellenthal, Garrett ; Hillier, Charles ; Hobart, Jeremy ; Hunt, Sarah E ; Jochim, Angela ; Kendall, Brian ; Kermode, Allan ; Kilpatrick, Trevor ; Langford, Cordelia ; Larsson, Malin ; Lathrop, Mark ; Lechner-Scott, Jeannette ; Lee, Michelle H ; Leppä, Virpi ; Lill, Christina M ; Lindén, Magdalena ; Lycke, Jan ; Macciardi, Fabio ; Manrique, Clara P ; Martinelli, Vittorio ; McCabe, Cristin ; Mero, Inger-Lise ; Nicholas, Richard ; Nilsson, Petra ; Piehl, Fredrik ; Quach, Hong ; Rodegher, Mariaemma ; Rog, David ; Salvetti, Marco ; Schnetz-Boutaud, Nathalie C ; Sellebjerg, Finn ; Schaefer, Catherine ; Siffrin, Volker ; Slee, Mark ; Sorosina, Melissa ; Sospedra, Mireia ; Sundqvist, Emilie ; Thorpe, John ; Ticca, Anna ; Visser, Elizabeth M ; Vucic, Steve ; Westerlind, Helga ; Wiley, James S ; Wilkins, Alastair ; Winkelmann, Juliane ; Zajicek, John ; Zindler, Eva ; Ivinson, Adrian J ; Hauser, Stephen L ; McVean, Gil

Nature genetics, 2013-11, Vol.45 (11), p.1353-1360 [Periódico revisado por pares]

United States: Nature Publishing Group

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7
Class II HLA interactions modulate genetic risk for multiple sclerosis
Class II HLA interactions modulate genetic risk for multiple sclerosis
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Class II HLA interactions modulate genetic risk for multiple sclerosis

Moutsianas, Loukas ; Jostins, Luke ; Beecham, Ashley H ; Dilthey, Alexander T ; Xifara, Dionysia K ; Ban, Maria ; Shah, Tejas S ; Patsopoulos, Nikolaos A ; Alfredsson, Lars ; Anderson, Carl A ; Attfield, Katherine E ; Baranzini, Sergio E ; Barrett, Jeffrey ; Binder, Thomas M C ; Booth, David ; Buck, Dorothea ; Celius, Elisabeth G ; Cotsapas, Chris ; D'Alfonso, Sandra ; Dendrou, Calliope A ; Donnelly, Peter ; Dubois, Bénédicte ; Fontaine, Bertrand ; Fugger, Lars ; Goris, An ; Gourraud, Pierre-Antoine ; Graetz, Christiane ; Hemmer, Bernhard ; Hillert, Jan ; Kockum, Ingrid ; Leslie, Stephen ; Lill, Christina M ; Martinelli-Boneschi, Filippo ; Oksenberg, Jorge R ; Olsson, Tomas ; Oturai, Annette ; Saarela, Janna ; Søndergaard, Helle Bach ; Spurkland, Anne ; Taylor, Bruce ; Winkelmann, Juliane ; Zipp, Frauke ; Haines, Jonathan L ; Pericak-Vance, Margaret A ; Spencer, Chris C A ; Stewart, Graeme ; Hafler, David A ; Ivinson, Adrian J ; Harbo, Hanne F ; Hauser, Stephen L ; De Jager, Philip L ; Compston, Alastair ; McCauley, Jacob L ; Sawcer, Stephen ; McVean, Gil

Nature genetics, 2015-10, Vol.47 (10), p.1107-1113 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients
Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients
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Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients

Özcelik, Hilmi ; Schmocker, Beverly ; Nicola, Nando Di ; Shi, Xiu-Hong ; Langer, Bernard ; Moore, Malcolm ; Taylor, Bryce R ; Narod, Steven A ; Darlington, Gerarda ; Andrulis, Irene L ; Gallinger, Steven ; Redston, Mark

Nature genetics, 1997-05, Vol.16 (1), p.17-18 [Periódico revisado por pares]

United States

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9
Recurrent activating mutations of G-protein-coupled receptor CYSLTR2 in uveal melanoma
Recurrent activating mutations of G-protein-coupled receptor CYSLTR2 in uveal melanoma
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Recurrent activating mutations of G-protein-coupled receptor CYSLTR2 in uveal melanoma

Moore, Amanda R ; Ceraudo, Emilie ; Sher, Jessica J ; Guan, Youxin ; Shoushtari, Alexander N ; Chang, Matthew T ; Zhang, Jenny Q ; Walczak, Edward G ; Kazmi, Manija A ; Taylor, Barry S ; Huber, Thomas ; Chi, Ping ; Sakmar, Thomas P ; Chen, Yu

Nature genetics, 2016-06, Vol.48 (6), p.675-680 [Periódico revisado por pares]

United States: Nature Publishing Group

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10
Genetic mapping across autoimmune diseases reveals shared associations and mechanisms
Genetic mapping across autoimmune diseases reveals shared associations and mechanisms
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Genetic mapping across autoimmune diseases reveals shared associations and mechanisms

Lincoln, Matthew R ; Connally, Noah ; Axisa, Pierre-Paul ; Gasperi, Christiane ; Mitrovic, Mitja ; van Heel, David ; Wijmenga, Cisca ; Withoff, Sebo ; Jonkers, Iris H ; Padyukov, Leonid ; Rich, Stephen S ; Graham, Robert R ; Gaffney, Patrick M ; Langefeld, Carl D ; Vyse, Timothy J ; Hafler, David A ; Chun, Sung ; Sunyaev, Shamil R ; Cotsapas, Chris

Nature genetics, 2024-05, Vol.56 (5), p.838-3 [Periódico revisado por pares]

United States: Nature Publishing Group

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Deste Autor:

  1. Ellison, D
  2. Taylor, M
  3. Peacock, J
  4. Mack, S
  5. Gillespie, Y

Neste Assunto:

  1. Genetics & Heredity
  2. Life Sciences & Biomedicine
  3. Science & Technology
  4. Humans
  5. Genetic Aspects

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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