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Refinado por: Biblioteca: FM - Fac. Medicina remover
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1
Autosome search for schizophrenia susceptibility genes in multiply affected families
Autosome search for schizophrenia susceptibility genes in multiply affected families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosome search for schizophrenia susceptibility genes in multiply affected families

M. I. Rees I Fenton; N. M Williams; P Holmans; N Norton; A Cardno; P Asherson; G Spurlock; Eric Roberts; E Parfitt; R Mant; Homero Pinto Vallada Filho; E Dawson; M. W Li; D. A Collier; J. F Powell; S Nanko; M Gill; Peter McGuffin; Michael J Owen

Molecular Psychiatry v. 4, n. 4, p. 353-359, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 1999 303 )(Acessar)

2
Autosome search for schizophrenia susceptibility genes in multiply affected families
Autosome search for schizophrenia susceptibility genes in multiply affected families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosome search for schizophrenia susceptibility genes in multiply affected families

M. I. Rees I Fenton; N. M Williams; P Holmans; N Norton; A Cardno; P Asherson; G Spurlock; Eric Roberts; E Parfitt; R Mant; Homero Pinto Vallada Filho; E Dawson; M. W Li; D. A Collier; J. F Powell; S Nanko; M Gill; Peter McGuffin; Michael J Owen

Molecular Psychiatry v. 4, n. 4, p. 353-359, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 1999 303 )(Acessar)

3
Sickled cell disease an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation
Sickled cell disease an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Sickled cell disease an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation

Eliane Gluckman Barbara Cappelli; Francoise Bernaudin; Myriam Labopin; Fernanda Volt; Jeanette Carreras; Belinda Pinto Simões; Alina Ferster; Sophie Dupont; Josu de la Fuente; Jean-Hugues Dalle; Marcos Zecca; Mark C Walters; Lakshmanan Krishnamurti; Monica Bhatia; Kathryn Leung; Gregory Yanik; Joanne Kurtzberg; Nathalie Dhedin; Mathieu Kuentz; Gerard Michel; Jane Apperley; Patrick Lutz; Bénédicte Neven; Ives Bertrand; Jean Pierre Vannier; Mouhab Ayas; Marina Cavazzana; Susanne Matthes Martin; Vanderson Amadeu da Rocha; Chantal Kenzey; Peter Bader; Franco Locatelli; Annalisa Ruggeri; Mary Eapen

Blood New York v. 129, n. 11, p. 1548-1556, 2017

New York 2017

Localização: FM - Fac. Medicina    (BCSEP 121 2017 )(Acessar)

4
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Material Type:
Artigo 		Adicionar ao Meu Espaço

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

Lea K. Davis Dongomei Yu; Clare L Keenan; Eric R Gamazon; Anuar I Konkashbaev; Eske M Derks; Benjamin M Neale; Jian Yang; S. Hong Lee; Patrick Evans; Cathy L Barr; Laura Bellodi; Fortu Benarroch; Gabriel Bedova Berrio; Oscar J Bienvenu; Michael H Bloch; Rianne M Blom; Ruth D Bruun; Cathy L Budman; Beatriz Camarena; Desmond Campbell; Carolina Cappi; Julio C. Cardona Salgado; Danielle C Cath; Maria C Cavallini; Denise A Chavira; Sylvain Chouinard; David V Conti; Edwin H Cook; Vladimir Coric; Bernadette A Cullen; Dieter Deforce; Richard Delorne; Yves Dion; Christopher K Edlund; Karin Egberts; Peter Falkai; Thomas V Fernandez; Patience J Gallagher; Helena Garrido; Daniel Geller; Simon L Girard; Hans J Grabe; Marco A Grados; Benjamin D Greenberg; Varda Gross Tsur; Stephen Haddad; Gary A Heiman; Sian M. J Hemmings; Ana G Hounie; Cornelia Illmann; Joseph Jankovic; Michael A Jenike; Robert A King; Barbara Kremeyer; Roger Kurlan; Nuria Lanzagorta; Marion Leboyer; James F Leckman; Leonhard Lennerts; Chunyu Liu; Christine Lochner; Thomas L Lowe; Fabio Macciardi; James T McCracken; Lauren MacGrant; Sandra C. Mesa Restrepo; Rainald Moessner; Jubel Morgan; Heike Muller; Dennis L Murphy; Allan L Naarden; William Cornejo Ochoa; Roel A Ophoff; Lisa Osieck; Andrew J Pakstis; Michele T Pato; Carlos N Pato; John Piacentini; Christopher Pittenger; Yehuda Pollak; Scott L Rauch; Tobias J Renner; Victor I Reus; Mark A Riddle; Mary M Robertson; Roxana Romero; Maria C Rosàrio; David Rosenberg; Guy A Rouleau; Stephan Ruhrmann; Andres Ruiz Linares; Aline S Sampaio; Jack Samuels; Paul Sandor; Brooke Sheppard; Harvey S Singer; Jan H Smit; Dan J Stein; E Strengman; Jay A Tischfield; Ana V. Valencia Duarte; Homero Pinto Vallada Filho; Filip Van Nieuwerburgh; Jeremy Veenstra VanderWeele; Susanne Walitza; Ying Wang; Jens R Wendland; Herman G. M Westenberg; Yin Yao Shugart; Eurípedes Constantino Miguel; William McMahon; Michael Wagner; Humberto Nicolini; Danielle Posthuma; Gregory L Hanna; Peter Heutink; Damiaan Denys; Paul D Arnold; Ben A Oostra; Gerald Nestadt; Nelson B Freimer; David L Pauls; Naomi R Wray; S. Evelyn Stewart; Carol A Mathews; James A Knowles; Nancy J Cox; Jeremiah M Scharf

Plos genetics San Francisco v. 9, n. 10, p. e1003864, 2013

San Francisco 2013

Localização: FM - Fac. Medicina    (BCSEP 483 2013 )(Acessar)

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Deste Autor:

  1. Vallada Filho, H
  2. Li, M
  3. Rees, M
  4. Nanko, S
  5. Dawson, E

Neste Assunto:

  1. Psiquiatria
  2. Genômica
  3. Sequenciamento Genético
  4. Fatores De Risco
  5. Anemia Falciforme

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

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