J. Partanen

发表

Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes

Beryl B. Cummings, John D. Eicher, Jonathan H. Chung, 2022, Communications Biology.

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Matthew S. Lebo, Beryl B. Cummings, John D. Eicher, 2021, Nature Medicine.

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

Pietro Della Briotta Parolo, Javier Gracia Tabuenca, John D. Eicher, 2019, Nature Communications.

Candidate gene region 15q26 and genetic susceptibility to coeliac disease in Finnish families.

M. Mäki, J. Partanen, K. Mustalahti, 2001, Scandinavian journal of gastroenterology.

FinnGen provides genetic insights from a well-phenotyped isolated population

Jacob C. Ulirsch, Benjamin B. Sun, Christopher N. Foley, 2023, Nature.

Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata

John D. Eicher, M. Obeidat, K. Kristiansson, 2023, Nature Communications.

FinnGen: Unique genetic insights from combining isolated population and national health register data

Aino, Pietro Della Briotta Parolo, Tuomo, 2022, medRxiv.

How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study

V. Salomaa, J. Kaprio, A. Palotie, 2022, Circulation. Genomic and precision medicine.

Accurate multi-population imputation of MICA, MICB, HLA-E, HLA-F and HLA-G alleles from genome SNP data

J. Ritari, S. Koskela, K. Hyvärinen, 2023, bioRxiv.

A comparative study of HLA genes in HLA-B27 positive ankylosing spondylitis and HLA-B27 positive peripheral reactive arthritis.

J. Partanen, M. Leirisalo-Repo, S. Koskimies, 1996, Arthritis and rheumatism.

Paper alert

K. Kaukinen, K. Kurppa, P. Saavalainen, 2009, Gastroenterology.

Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q.

L. Peltonen, J. Terwilliger, J. Kaprio, 1999, American journal of human genetics.

Development of mesothelioma-specific oncolytic immunotherapy enabled by immunopeptidomics of murine and human mesothelioma tumors

Rui M. M. Branca, J. Lehtiö, V. Cerullo, 2023, Nature communications.

the genetic etiology

Beryl B. Cummings, John D. Eicher, W. M. van der Flier, 2023 .

The role of polygenic risk and susceptibility genes in breast cancer over the course of life

Beryl B. Cummings, John D. Eicher, M. Pirinen, 2020, Nature Communications.

A machine-learning method for biobank-scale genetic prediction of blood group antigens

J. Ritari, K. Hyvärinen, K. Haimila, 2023, medRxiv.

Communicating polygenic and non-genetic risk for atherosclerotic cardiovascular disease - An observational follow-up study

V. Salomaa, J. Kaprio, A. Palotie, 2020, medRxiv.

Oral and non-oral lichen planus show genetic heterogeneity and differential risk for autoimmune disease and oral cancer

S. Ripatti, J. Karjalainen, M. Reeve, 2024, American journal of human genetics.

Hippocampal sclerosis in refractory temporal lobe epilepsy is associated with gluten sensitivity

K. Kaukinen, J. Peltola, Jukka Partanen, 2009, Journal of Neurology, Neurosurgery, and Psychiatry.

Killer-cell immunoglobulin-like receptor ligand compatibility in the outcome of Finnish unrelated donor hematopoietic stem cell transplantation.

J. Partanen, K. Porkka, K. Vettenranta, 2007, Transplant immunology.

Endomysial antibody-negative coeliac disease: clinical characteristics and intestinal autoantibody deposits

L. Lorand, K. Kaukinen, I. Korponay-Szabó, 2006, Gut.

A FinnGen pilot clinical recall study for Alzheimer’s disease

Pietro Della Briotta Parolo, John D. Eicher, M. Obeidat, 2023, medRxiv.

Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population.

J. Partanen, R. Voutilainen, A. Levo, 1997, The Journal of clinical endocrinology and metabolism.

Immunoglobulin A autoantibodies against transglutaminase 2 in the small intestinal mucosa predict forthcoming coeliac disease

K. Kaukinen, I. Korponay-Szabó, M. Mäki, 2006, Alimentary pharmacology & therapeutics.

CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study.

Mikko Arvas, P. Sistonen, J. Partanen, 1999, Tissue antigens.

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

John D. Eicher, Audrey Y. Chu, M. Pirinen, 2019, European Journal of Human Genetics.

Proteomic aging clock predicts mortality and risk of common age-related diseases in diverse populations

M. Kurki, N. Amin, A. Nevado-Holgado, 2023, medRxiv.

Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

Javier Gracia Tabuenca, John D. Eicher, A. Auton, 2020, Nature.

Phenome-wide HLA association study of Finnish biobankparticipants reveals infection-autoimmune disease linksand modifier effects between HLA genes and alleles

J. Partanen, J. Ritari, S. Koskela, 2020, medRxiv.

Heme oxygenase 1 gene polymorphisms and outcome of renal transplantation

K. Salmela, J. Partanen, L. Kyllönen, 2007, International journal of immunogenetics.

Gamete-level immunogenetic incompatibility in humans–towards deeper understanding of fertilization and infertility?

J. Kekäläinen, J. Ritari, S. Koskela, 2020, Heredity.

Platelet alloantigens HPA‐1, ‐2, ‐3, ‐5 and ‐6b in Finns

J. Partanen, R. Kekomäki, Jukka Partanen, 1995, Transfusion medicine.

Morphological single-cell analysis of peripheral blood mononuclear cells from 390 healthy blood donors with Blood Cell Painting

L. Paavolainen, V. Pietiäinen, R. Rodosthenous, 2024, bioRxiv.