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Jukka Partanen
Jukka Partanen
Research director, FRC Blood Service, Helsinki, Finland
Geverifieerd e-mailadres voor veripalvelu.fi
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HLA types in celiac disease patients not carrying the DQA1* 05-DQB1* 02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease
K Karell, AS Louka, SJ Moodie, H Ascher, F Clot, L Greco, PJ Ciclitira, ...
Human immunology 64 (4), 469-477, 2003
8312003
FinnGen provides genetic insights from a well-phenotyped isolated population
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ...
Nature 613 (7944), 508-518, 2023
6632023
Celiac disease risk in the USA: high prevalence of antiendomysium antibodies in healthy blood donors
T Not, K Horvath, ID Hill, J Partanen, A Hammed, G Magazzu, A Fasano
Scandinavian journal of gastroenterology 33 (5), 494-498, 1998
4921998
Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus
G Thomson, WP Robinson, MK Kuhner, S Joe, MJ MacDonald, ...
American journal of human genetics 43 (6), 799, 1988
4571988
Celiac disease in patients with severe liver disease: gluten-free diet may reverse hepatic failure
K Kaukinen, L Halme, P Collin, M Färkkilä, M Mäki, P Vehmanen, ...
Gastroenterology 122 (4), 881-888, 2002
3782002
HLA-DQ typing in the diagnosis of celiac disease
K Kaukinen, J Partanen, M Mäki, P Collin
Official journal of the American College of Gastroenterology| ACG 97 (3 …, 2002
3592002
FinnGen: Unique genetic insights from combining isolated population and national health register data
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ...
MedRxiv, 2022.03. 03.22271360, 2022
3442022
Diagnosing mild enteropathy celiac disease: a randomized, controlled clinical study
K Kurppa, P Collin, M Viljamaa, K Haimila, P Saavalainen, J Partanen, ...
Gastroenterology 136 (3), 816-823, 2009
3262009
Endomysial antibody-negative coeliac disease: clinical characteristics and intestinal autoantibody deposits
TT Salmi, P Collin, IR Korponay-Szabo, K Laurila, J Partanen, H Huhtala, ...
Gut 55 (12), 1746-1753, 2006
3232006
Secretor genotype (FUT2 gene) is strongly associated with the composition of Bifidobacteria in the human intestine
P Wacklin, H Mäkivuokko, N Alakulppi, J Nikkilä, H Tenkanen, J Räbinä, ...
PloS one 6 (5), e20113, 2011
3022011
Elevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiency
IR Korponay-Szabó, I Dahlbom, K Laurila, S Koskinen, N Woolley, ...
Gut 52 (11), 1567-1571, 2003
2792003
Genetic susceptibility to severe course of nephropathia epidemica caused by Puumala hantavirus
J Mustonen, J Partanen, M Kanerva, K Pietilä, O Vapalahti, A Pasternack, ...
Kidney international 49 (1), 217-221, 1996
2701996
The duodenal microbiota composition of adult celiac disease patients is associated with the clinical manifestation of the disease
P Wacklin, K Kaukinen, E Tuovinen, P Collin, K Lindfors, J Partanen, ...
Inflammatory bowel diseases 19 (5), 934-941, 2013
2442013
AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype
M Halonen, P Eskelin, AG Myhre, J Perheentupa, ES Husebye, ...
The Journal of Clinical Endocrinology & Metabolism 87 (6), 2568-2574, 2002
2342002
Celiac disease without villous atrophy
K Kaukinen, M Mãki, J Partanen, H Sievãnen, P Collin
Digestive diseases and sciences 46, 879-887, 2001
2342001
Celiac disease and markers of celiac disease latency in patients with primary Sjögren’s syndrome
S Iltanen, P Collin, M Korpela, K Holm, J Partanen, A Polvi, M Mäki
The American journal of gastroenterology 94 (4), 1042-1046, 1999
2061999
Persistent small bowel mucosal villous atrophy without symptoms in coeliac disease
K Kaukinen, M Peräaho, K Lindfors, J Partanen, N Woolley, P Pikkarainen, ...
Alimentary pharmacology & therapeutics 25 (10), 1237-1245, 2007
2002007
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 Jääskeläinen, A Levo, R Voutilainen, J Partanen
The Journal of Clinical Endocrinology & Metabolism 82 (10), 3293-3297, 1997
1961997
Multiplex, fluorescent, solid-phase minisequencing for efficient screening of DNA sequence variation
T Pastinen, J Partanen, AC Syvänen
Clinical Chemistry 42 (9), 1391-1397, 1996
1931996
Small-bowel mucosal transglutaminase 2-specific IgA deposits in coeliac disease without villous atrophy: a prospective and randomized clinical study
K Kaukinen, M Peräaho, P Collin, J Partanen, N Woolley, T Kaartinen, ...
Scandinavian journal of gastroenterology 40 (5), 564-572, 2005
1762005
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Artikelen 1–20