Torthaí cuardaigh - Aarno Palotie
- 1 - 20 toradh as 265 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Use of population isolates for mapping complex traits de réir Leena Peltonen, Aarno Palotie, Kenneth Lange
Foilsithe / Cruthaithe 2000Revisão -
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Lessons from studying monogenic disease for common disease de réir Leena Peltonen, Markus Perola, Jussi Naukkarinen, Aarno Palotie
Foilsithe / Cruthaithe 2006Revisão -
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Systematic review of genome-wide expression studies in multiple sclerosis de réir A K Kemppinen, Jaakko Kaprio, Aarno Palotie, Janna Saarela
Foilsithe / Cruthaithe 2011Artigo -
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Patterns of Inheritance of Constitutional Delay of Growth and Puberty in Families of Adolescent Girls and Boys Referred to Specialist Pediatric Care de réir Karoliina Wehkalampi, Elisabeth Widén, Tiina Laine, Aarno Palotie, Leo Dunkel
Foilsithe / Cruthaithe 2007Artigo -
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Genetic Risk Prediction and a 2-Stage Risk Screening Strategy for Coronary Heart Disease de réir Emmi Tikkanen, Aki S. Havulinna, Aarno Palotie, Veikko Salomaa, Samuli Ripatti
Foilsithe / Cruthaithe 2013Artigo -
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Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levels de réir Hanna Mikkola, Martti Syrjälä, Vesa Rasi, Elina Vahtera, Eija Hämäläinen, Leena Peltonen, Aarno Palotie
Foilsithe / Cruthaithe 1994Artigo -
11
Genomic Organization of Human and Mouse Genes for Vascular Endothelial Growth Factor C de réir Dmitri Chilov, Eola Kukk, Suvi Taira, Michael Jeltsch, Jaakko Kaukonen, Aarno Palotie, Vladimir Joukov, Kari Alitalo
Foilsithe / Cruthaithe 1997Artigo -
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Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in <i>MUC5B</i> mutation carriers de réir Antti Palomäki, Aarno Palotie, Jukka Koskela, Kari K. Eklund, Matti Pirinen, Samuli Ripatti, Tarja Laitinen, Nina Mars
Foilsithe / Cruthaithe 2021Artigo -
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A Comparison of the Whole Genome Approach of MeDIP-Seq to the Targeted Approach of the Infinium HumanMethylation450 BeadChip® for Methylome Profiling de réir Christine Clark, Priit Palta, Christopher J. Joyce, Carol Scott, Elin Grundberg, Panos Deloukas, Aarno Palotie, Alison J. Coffey
Foilsithe / Cruthaithe 2012Artigo -
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Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16 de réir Kaisu Keskitalo, Antti Knaapila, Mikko Kallela, Aarno Palotie, Maija Wessman, Sampo Sammalisto, Leena Peltonen, Hely Tuorila, Markus Perola
Foilsithe / Cruthaithe 2007Artigo -
16
Tissue microarray analysis of cytoskeletal actin‐associated biomarkers gelsolin and E‐cadherin in urothelial carcinoma de réir Jianyu Rao, David B. Seligson, Harri Visapää, Steve Horvath, Mervi Eeva, Kia Michel, Allan Pantuck, Arie S. Belldegrun, Aarno Palotie
Foilsithe / Cruthaithe 2002Artigo -
17
Describing the genetic architecture of epilepsy through heritability analysis de réir Doug Speed, Terence J. O’Brien, Aarno Palotie, Kirill Shkura, Anthony G Marson, David J. Balding, Michael R. Johnson
Foilsithe / Cruthaithe 2014Artigo -
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Bmx Tyrosine Kinase Has a Redundant Function Downstream of Angiopoietin and Vascular Endothelial Growth Factor Receptors in Arterial Endothelium de réir Iiro Rajantie, Niklas Ekman, Kristiina Iljin, Elena Arighi, Yuji Gunji, Jaakko Kaukonen, Aarno Palotie, Mieke Dewerchin, Peter Carmeliet, Kari Alitalo
Foilsithe / Cruthaithe 2001Artigo -
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Neural, not gonadal, origin of brain sex differences in a gynandromorphic finch de réir Robert J. Agate, William Grisham, Juli Wade, Suzanne M. Mann, John C. Wingfield, Carolyn Schanen, Aarno Palotie, Arthur P. Arnold
Foilsithe / Cruthaithe 2003Artigo -
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Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events de réir Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, Reetta Kälviäinen, Mark J. Daly
Foilsithe / Cruthaithe 2024Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Medicine
Genotype
Internal medicine
Single-nucleotide polymorphism
Genome-wide association study
Genetic association
Computational biology
Population
Disease
Psychiatry
Psychology
Bioinformatics
Environmental health
Phenotype
Endocrinology
Genome
Sociology
Demography
Computer science
Evolutionary biology
Mutation
Neuroscience
Pathology
Allele
Biochemistry
Genetic variation
Immunology