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1
Tau haplotypes support the Asian ancestry of the Roma population settled in the Basque Country
Tau haplotypes support the Asian ancestry of the Roma population settled in the Basque Country
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Tau haplotypes support the Asian ancestry of the Roma population settled in the Basque Country

Alfonso-Sánchez, Miguel A ; Espinosa, Ibone ; Gómez-Pérez, Luis ; Poveda, Alaitz ; Rebato, Esther ; Peña, Jose A

Heredity, 2018-01, Vol.120 (2), p.91-99 [Periódico revisado por pares]

England: Springer Nature B.V

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2
Alcohol use disorder and divorce: evidence for a genetic correlation in a population‐based Swedish sample
Alcohol use disorder and divorce: evidence for a genetic correlation in a population‐based Swedish sample
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Alcohol use disorder and divorce: evidence for a genetic correlation in a population‐based Swedish sample

Salvatore, Jessica E. ; Larsson Lönn, Sara ; Sundquist, Jan ; Lichtenstein, Paul ; Sundquist, Kristina ; Kendler, Kenneth S.

Addiction (Abingdon, England), 2017-04, Vol.112 (4), p.586-593 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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3
Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium
Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium
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Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium

Heckman, Michael G. ; Soto-Ortolaza, Alexandra I. ; Aasly, Jan O. ; Abahuni, Nadine ; Annesi, Grazia ; Bacon, Justin A. ; Bardien, Soraya ; Bozi, Maria ; Brice, Alexis ; Brighina, Laura ; Carr, Jonathan ; Chartier-Harlin, Marie-Christine ; Dardiotis, Efthimios ; Dickson, Dennis W. ; Diehl, Nancy N. ; Elbaz, Alexis ; Ferrarese, Carlo ; Fiske, Brian ; Gibson, J. Mark ; Gibson, Rachel ; Hadjigeorgiou, Georgios M. ; Hattori, Nobutaka ; Ioannidis, John P.A. ; Boczarska-Jedynak, Magdalena ; Jasinska-Myga, Barbara ; Jeon, Beom S. ; Kim, Yun Joong ; Klein, Christine ; Kruger, Rejko ; Kyratzi, Elli ; Lesage, Suzanne ; Lin, Chin-Hsien ; Lynch, Timothy ; Maraganore, Demetrius M. ; Mellick, George D. ; Mutez, Eugénie ; Nilsson, Christer ; Opala, Grzegorz ; Park, Sung Sup ; Petrucci, Simona ; Puschmann, Andreas ; Quattrone, Aldo ; Sharma, Manu ; Silburn, Peter A. ; Sohn, Young Ho ; Stefanis, Leonidas ; Tadic, Vera ; Theuns, Jessie ; Tomiyama, Hiroyuki ; Uitti, Ryan J. ; Valente, Enza Maria ; Van Broeckhoven, Christine ; van de Loo, Simone ; Vassilatis, Demetrios K. ; Vilariño-Güell, Carles ; White, Linda R. ; Wirdefeldt, Karin ; Wszolek, Zbigniew K. ; Wu, Ruey-Meei ; Hentati, Faycal ; Farrer, Matthew J. ; Ross, Owen A.

Movement disorders, 2013-10, Vol.28 (12), p.1740-1744 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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4
Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus
Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus
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Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus

Arora, G. P. ; Åkerlund, M. ; Brøns, C. ; Moen, G.‐H. ; Wasenius, N. S. ; Sommer, C. ; Jenum, A. K. ; Almgren, P. ; Thaman, R. G. ; Orho‐Melander, M. ; Eriksson, J. ; Qvigstad, E. ; Birkeland, K. ; Berntorp, K. ; Vaag, A. A. ; Groop, L. ; Prasad, R. B.

Journal of internal medicine, 2019-08, Vol.286 (2), p.192-206 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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5
Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population-based cohort
Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population-based cohort
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Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population-based cohort

Lannoy, Séverine ; Ohlsson, Henrik ; Stephenson, Mallory ; Sundquist, Jan ; Sundquist, Kristina ; Edwards, Alexis C

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2024-02, p.e32974-e32974 [Periódico revisado por pares]

United States

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6
Risk of non‐fatal suicide attempt in individuals with substance use disorder: the roles of aggregate genetic liability and environmental exposures in a Swedish population‐based cohort
Risk of non‐fatal suicide attempt in individuals with substance use disorder: the roles of aggregate genetic liability and environmental exposures in a Swedish population‐based cohort
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Risk of non‐fatal suicide attempt in individuals with substance use disorder: the roles of aggregate genetic liability and environmental exposures in a Swedish population‐based cohort

Lannoy, Séverine ; Ohlsson, Henrik ; Stephenson, Mallory ; Kendler, Kenneth S. ; Sundquist, Jan ; Sundquist, Kristina ; Edwards, Alexis C.

Addiction (Abingdon, England), 2022-11, Vol.117 (11), p.2943-2952 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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7
Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children
Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children
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Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children

Lundvall, Mikael ; Rajaei, Saideh ; Erlandson, Anna ; Kyllerman, Mårten

Acta Paediatrica, 2012-01, Vol.101 (1), p.85-91 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
Genetic and environmental contributions to the association between ADHD and affective problems in early childhood—A Swedish population‐based twin study
Genetic and environmental contributions to the association between ADHD and affective problems in early childhood—A Swedish population‐based twin study
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Genetic and environmental contributions to the association between ADHD and affective problems in early childhood—A Swedish population‐based twin study

Rydell, Mina ; Taylor, Mark J. ; Larsson, Henrik

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-07, Vol.174 (5), p.538-546 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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9
Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease
Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease
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Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease

Johansson, Anna M. ; Halldén, Christer ; Säll, Torbjörn ; Lethagen, Stefan

Annals of human genetics, 2011-07, Vol.75 (4), p.447-455 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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10
Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3
Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3
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Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: Suggestive linkage to 10q23.32-q25.3

Bergman, Annika ; Karlsson, Per ; Berggren, Jonna ; Martinsson, Tommy ; Björck, Karin ; Nilsson, Staffan ; Wahlström, Jan ; Wallgren, Arne ; Nordling, Margareta

Genes chromosomes & cancer, 2007-03, Vol.46 (3), p.302-309 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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