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MANF protects human pancreatic beta cells against stress-induced cell death.
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- Diabetologia, 2018, v. 61, n. 10, p. 2202, doi. 10.1007/s00125-018-4687-y
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- Article
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
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- Journal of Human Genetics, 2015, v. 60, n. 7, p. 399, doi. 10.1038/jhg.2015.37
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- Article
CELSR2 is a candidate susceptibility gene in idiopathic scoliosis.
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- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189591
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- Article
Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease.
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- BMC Pulmonary Medicine, 2016, v. 16, p. 1, doi. 10.1186/s12890-016-0309-y
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- Article
Viral infection‐related gene upregulation in monocytes in children with signs of β‐cell autoimmunity.
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- Pediatric Diabetes, 2022, v. 23, n. 6, p. 703, doi. 10.1111/pedi.13346
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- Article
Tyrosine kinase 2 and interferon regulatory factor 5 polymorphisms are associated with discoid and subacute cutaneous lupus erythematosus.
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- Experimental Dermatology, 2010, v. 19, n. 2, p. 123, doi. 10.1111/j.1600-0625.2009.00982.x
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- Article
Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-44882-0
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- Article
A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29011-7
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- Article
Association study of the IL18RAP locus in three European populations with coeliac disease.
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- Human Molecular Genetics, 2009, v. 18, n. 6, p. 1148, doi. 10.1093/hmg/ddn438
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- Article
A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception.
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- Human Molecular Genetics, 2004, v. 13, n. 8, p. 799, doi. 10.1093/hmg/ddh096
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- Article
Linkage but Not Association of Calpain-10 to Type 2 Diabetes Replicated in Northern Sweden.
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- Diabetes, 2006, v. 55, n. 6, p. 1879, doi. 10.2337/db05-1495
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- Article
Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations.
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- European Journal of Human Genetics, 2011, v. 19, n. 6, p. 682, doi. 10.1038/ejhg.2011.2
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- Article
The CTLA4 region as a general autoimmunity factor: An extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease.
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- European Journal of Human Genetics, 2003, v. 11, n. 1, p. 81, doi. 10.1038/sj.ejhg.5200903
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- Article
Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report.
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01020-2
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- Article
The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50334-6
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- Article
Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults.
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- Cerebral Cortex, 2024, v. 34, n. 4, p. 1, doi. 10.1093/cercor/bhae144
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- Article
Homozygosity mapping of familial glioma in Northern Sweden.
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- Acta Oncologica, 2005, v. 44, n. 2, p. 114, doi. 10.1080/02841860510007558
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- Article
Polymorphisms of the ITGAM Gene Confer Higher Risk of Discoid Cutaneous Than of Systemic Lupus Erythematosus.
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- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0014212
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- Article
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.
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- Human Genetics, 2015, v. 134, n. 11/12, p. 1239, doi. 10.1007/s00439-015-1602-1
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- Article
Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.
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- Scientific Reports, 2016, p. 33240, doi. 10.1038/srep33240
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- Article
Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples.
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- Scientific Reports, 2016, p. 33256, doi. 10.1038/srep33256
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- Article
Corrigendum: Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos.
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- Scientific Reports, 2016, p. 32053, doi. 10.1038/srep32053
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- Article
Globin mRNA reduction for whole-blood transcriptome sequencing.
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- Scientific Reports, 2016, p. 31584, doi. 10.1038/srep31584
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- Article
Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos.
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- Scientific Reports, 2016, p. 28995, doi. 10.1038/srep28995
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- Article
Mlh1 deficiency in normal mouse colon mucosa associates with chromosomally unstable colon cancer.
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- Carcinogenesis, 2018, v. 39, n. 6, p. 788, doi. 10.1093/carcin/bgy056
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- Article
Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma.
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- Acta Dermato-Venereologica, 2020, v. 100, n. 2, p. 1, doi. 10.2340/00015555-3404
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- Article
The genetic population structure of northern Sweden and its implications for mapping genetic diseases.
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- Hereditas, 2007, v. 144, n. 5, p. 171, doi. 10.1111/j.2007.0018-0661.02007.x
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- Article
Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.
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- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01190
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- Article
IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease.
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- BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-8
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- Article
Human endometrial cell-type-specific RNA sequencing provides new insights into the embryo–endometrium interplay.
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- Human Reproduction Open, 2022, v. 2022, n. 4, p. 1, doi. 10.1093/hropen/hoac043
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- Article
Long-chain polyphosphates inhibit type I interferon signaling and augment LPS-induced cytokine secretion in human leukocytes.
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- Journal of Leukocyte Biology, 2023, v. 114, n. 3, p. 250, doi. 10.1093/jleuko/qiad058
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- Article
A2ML1 and otitis media: novel variants, differential expression, and relevant pathways.
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- Human Mutation, 2019, v. 40, n. 8, p. 1156, doi. 10.1002/humu.23769
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- Article
The role of CDHR3 in susceptibility to otitis media.
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- Journal of Molecular Medicine, 2021, v. 99, n. 11, p. 1571, doi. 10.1007/s00109-021-02118-7
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- Article
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
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- eLife, 2024, p. 1, doi. 10.7554/eLife.89762
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- Article
Novel TMEM173 Mutation and the Role of Disease Modifying Alleles.
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- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02770
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- Article
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.
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- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3986, doi. 10.1093/hmg/ddy306
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- Article
Current Knowledge of the Genetics of Otitis Media.
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- Current Allergy & Asthma Reports, 2012, v. 12, n. 6, p. 582, doi. 10.1007/s11882-012-0292-1
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- Article
Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods.
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- BMC Bioinformatics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12859-019-3017-9
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- Article
Moritella viscosa in lumpfish (Cyclopterus lumpus) and Atlantic salmon (Salmo salar).
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- Journal of Fish Diseases, 2018, v. 41, n. 11, p. 1751, doi. 10.1111/jfd.12884
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- Article
Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb<sup>-/-</sup> Microglia.
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- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0158195
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- Article
Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus.
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- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0132551
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- Article
Effects of exercise on whole‐blood transcriptome profile in children with overweight/obesity.
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- American Journal of Human Biology, 2024, v. 36, n. 2, p. 1, doi. 10.1002/ajhb.23983
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- Article