Next-generation sequencing technologies and applications for human genetic history and forensics

Por Berglund, Eva C, Kiialainen, Anna, Syvänen, Ann-Christine
Publicado em 2011

Detecting imbalanced expression of SNP alleles by minisequencing on microarrays

Por Dahlgren Andreas, Fredriksson Mona, Liljedahl Ulrika, Syvänen Ann-Christine
Publicado em 2004-10-01

Minisequencing on oligonucleotide microarrays: comparison of immobilisation chemistries

Por Lindroos, Katarina, Liljedahl, Ulrika, Raitio, Mirja, Syvänen, Ann-Christine
Publicado em 2001

Detecting imbalanced expression of SNP alleles by minisequencing on microarrays

Por Liljedahl, Ulrika, Fredriksson, Mona, Dahlgren, Andreas, Syvänen, Ann-Christine
Publicado em 2004

Silhouette scores for assessment of SNP genotype clusters

Por Lovmar, Lovisa, Ahlford, Annika, Jonsson, Mats, Syvänen, Ann-Christine
Publicado em 2005

Heteroplasmy of the Human mtDNA Control Region Remains Constant during Life

Por Lagerström-Fermér, Maria, Olsson, Charlotta, Forsgren, Lars, Syvänen, Ann-Christine
Publicado em 2001

Multiplex SNP genotyping in pooled DNA samples by a four-colour microarray system

Por Lindroos, Katarina, Sigurdsson, Snaevar, Johansson, Karin, Rönnblom, Lars, Syvänen, Ann-Christine
Publicado em 2002

Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA

Por Lovmar, Lovisa, Fredriksson, Mona, Liljedahl, Ulrika, Sigurdsson, Snaevar, Syvänen, Ann-Christine
Publicado em 2003

Association of the Estrogen Receptor 1 (ESR1) Gene with Body Height in Adult Males from Two Swedish Population Cohorts

Por Dahlgren, Andreas, Lundmark, Per, Axelsson, Tomas, Lind, Lars, Syvänen, Ann-Christine
Publicado em 2008

DNA Methylation Analysis of Bone Marrow Cells at Diagnosis of Acute Lymphoblastic Leukemia and at Remission

Por Nordlund, Jessica, Milani, Lili, Lundmark, Anders, Lönnerholm, Gudmar, Syvänen, Ann-Christine
Publicado em 2012

Microarrays for Genotyping Human Group A Rotavirus by Multiplex Capture and Type-Specific Primer Extension

Por Lovmar, Lovisa, Fock, Caroline, Espinoza, Felix, Bucardo, Filemon, Syvänen, Ann-Christine, Bondeson, Kåre
Publicado em 2003

A System for Specific, High-throughput Genotyping by Allele-specific Primer Extension on Microarrays

Por Pastinen, Tomi, Raitio, Mirja, Lindroos, Katarina, Tainola, Päivi, Peltonen, Leena, Syvänen, Ann-Christine
Publicado em 2000

Single nucleotide polymorphisms in the apolipoprotein B and low density lipoprotein receptor genes affect response to antihypertensive treatment

Por Liljedahl, Ulrika, Lind, Lars, Kurland, Lisa, Berglund, Lars, Kahan, Thomas, Syvänen, Ann-Christine
Publicado em 2004

Coffee consumption and CYP1A2 genotype in relation to bone mineral density of the proximal femur in elderly men and women: a cohort study

Por Hallström, Helena, Melhus, Håkan, Glynn, Anders, Lind, Lars, Syvänen, Ann-Christine, Michaëlsson, Karl
Publicado em 2010

Performance of Microarray and Liquid Based Capture Methods for Target Enrichment for Massively Parallel Sequencing and SNP Discovery

Por Kiialainen, Anna, Karlberg, Olof, Ahlford, Annika, Sigurdsson, Snaevar, Lindblad-Toh, Kerstin, Syvänen, Ann-Christine
Publicado em 2011

Y-Chromosomal SNPs in Finno–Ugric-Speaking Populations Analyzed by Minisequencing on Microarrays

Por Raitio, Mirja, Lindroos, Katarina, Laukkanen, Minna, Pastinen, Tomi, Sistonen, Pertti, Sajantila, Antti, Syvänen, Ann-Christine
Publicado em 2001

Sex chromosome evolution and speciation in Ficedula flycatchers.

Por Saetre, Glenn-Peter, Borge, Thomas, Lindroos, Katarina, Haavie, Jon, Sheldon, Ben C, Primmer, Craig, Syvänen, Ann-Christine
Publicado em 2003

Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells

Por Milani, Lili, Gupta, Manu, Andersen, Malin, Dhar, Sumeer, Fryknäs, Mårten, Isaksson, Anders, Larsson, Rolf, Syvänen, Ann-Christine
Publicado em 2007

CopyNumber450kCancer: baseline correction for accurate copy number calling from the 450k methylation array

Por Marzouka, Nour-al-dain, Nordlund, Jessica, Bäcklin, Christofer L., Lönnerholm, Gudmar, Syvänen, Ann-Christine, Carlsson Almlöf, Jonas
Publicado no Bioinformatics (2016)

A novel splicing mutation in the IQSEC2 gene that modulates the phenotype severity in a family with intellectual disability

Por Madrigal, Irene, Alvarez-Mora, Maria Isabel, Rosell, Jordi, Rodríguez-Revenga, Laia, Karlberg, Olof, Sauer, Sascha, Syvänen, Ann-Christine, Mila, Montserrat
Publicado no Eur J Hum Genet (2016)