Fatty acid metabolism in adipose tissue, muscle and liver in health and disease. by Frayn, K, Arner, P, Yki-Järvinen, H

Dietary carbohydrates and fats in nonalcoholic fatty liver disease by Yki-Järvinen, H, Luukkonen, PK, Hodson, L, Moore, JB

Liver fat and lipid oxidation in humans. by Kotronen, A, Seppälä-Lindroos, A, Vehkavaara, S, Bergholm, R, Frayn, K, Fielding, B, Yki-Järvinen, H

A clinical audit programme for diagnostic radiology: The approach adopted by the international atomic energy agency by Faulkner, K., Jarvinen, H., Butler, P., McLean, I.D., Pentecost, M., Rickard, M., Abdullah, B.

Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci. by Niittymäki, I, Tuupanen, S, Li, Y, Järvinen, H, Mecklin, J, Tomlinson, I, Houlston, R, Karhu, A, Aaltonen, L

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients. by Enholm, S, Hienonen, T, Suomalainen, A, Lipton, L, Tomlinson, I, Kärjä, V, Eskelinen, M, Mecklin, J, Karhu, A, Järvinen, H, Aaltonen, L

Mutations in the SMAD4/DPC4 gene in juvenile polyposis. by Howe, JR, Roth, S, Ringold, J, Summers, R, Järvinen, H, Sistonen, P, Tomlinson, I, Houlston, R, Bevan, S, Mitros, F, Stone, E, Aaltonen, L

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis by Kokko, A, Laiho, P, Lehtonen, R, Korja, S, Carvajal-Carmona, L, Järvinen, H, Mecklin, J, Eng, C, Schleutker, J, Tomlinson, I, Vahteristo, P, Aaltonen, L

Splanchnic balance of free fatty acids, endocannabinoids and lipids in subjects with NAFLD by Kotronen, A, Westerbacka, J, Fielding, B, Wahren, J, Hodson, L, Seppanen-Laakso, T, Suortti, T, Arola, J, Hultcrantz, R, Castillo, S, Frayn, K, Oresic, M, Yki-Jarvinen, H

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. by Hemminki, A, Tomlinson, I, Markie, D, Järvinen, H, Sistonen, P, Björkqvist, A, Knuutila, S, Salovaara, R, Bodmer, W, Shibata, D, de la Chapelle, A, Aaltonen, L

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome. by Volikos, E, Robinson, J, Aittomäki, K, Mecklin, J, Järvinen, H, Westerman, A, de Rooji, F, Vogel, T, Moeslein, G, Launonen, V, Tomlinson, I, Silver, A, Aaltonen, L

Splanchnic balance of free fatty acids, endocannabinoids, and lipids in subjects with nonalcoholic fatty liver disease. by Westerbacka, J, Kotronen, A, Fielding, B, Wahren, J, Hodson, L, Perttilä, J, Seppänen-Laakso, T, Suortti, T, Arola, J, Hultcrantz, R, Castillo, S, Olkkonen, V, Frayn, K, Orešič, M, Yki-Järvinen, H

Effect of short-term carbohydrate overfeeding and long-term weight loss on liver fat in overweight humans. by Sevastianova, K, Santos, A, Kotronen, A, Hakkarainen, A, Makkonen, J, Silander, K, Peltonen, M, Romeo, S, Lundbom, J, Lundbom, N, Olkkonen, V, Gylling, H, Fielding, B, Rissanen, A, Yki-Järvinen, H

Mutations in Exon 1 Highlight the Role of MED12 in Uterine Leiomyomas by Kämpjärvi, K, Park, M, Mehine, M, Kim, N, Clark, A, Bützow, R, Böhling, T, Böhm, J, Mecklin, J, Järvinen, H, Tomlinson, I, van der Spuy, Z, Sjöberg, J, Boyer, T, Vahteristo, P

Mutations in exon 1 highlight the role of MED12 in uterine leiomyomas by Kämpjärvi, K, Park, M, Mehine, M, Kim, N, Clark, A, Bützow, R, Böhling, T, Böhm, J, Mecklin, J, Järvinen, H, Tomlinson, I, van der Spuy, Z, Sjöberg, J, Boyer, T, Vahteristo, P

Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases. by Laiho, P, Hienonen, T, Karhu, A, Lipton, L, Aalto, Y, Thomas, H, Birkenkamp-Demtroder, K, Hodgson, S, Salovaara, R, Mecklin, J, Järvinen, H, Knuutila, S, Halford, S, Ørntoft, T, Tomlinson, I, Launonen, V, Houlston, R, Aaltonen, L

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. by Ylikorkala, A, Avizienyte, E, Tomlinson, I, Tiainen, M, Roth, S, Loukola, A, Hemminki, A, Johansson, M, Sistonen, P, Markie, D, Neale, K, Phillips, R, Zauber, P, Twama, T, Sampson, J, Järvinen, H, Mäkelä, T, Aaltonen, L

Human PNPLA3-I148M variant increases hepatic retention of polyunsaturated fatty acids by Luukkonen, PK, Nick, A, Hölttä-Vuori, M, Thiele, C, Isokuortti, E, Lallukka-Brück, S, Zhou, Y, Hakkarainen, A, Lundbom, N, Peltonen, M, Orho-Melander, M, Orešič, M, Hyötyläinen, T, Hodson, L, Ikonen, E, Yki-Järvinen, H

The C/C-13910 genotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population. by Rasinperä, H, Forsblom, C, Enattah, N, Halonen, P, Salo, K, Victorzon, M, Mecklin, J, Järvinen, H, Enholm, S, Sellick, G, Alazzouzi, H, Houlston, R, Robinson, J, Groop, P, Tomlinson, I, Schwartz, S, Aaltonen, L, Järvelä, I

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. by Hemminki, A, Markie, D, Tomlinson, I, Avizienyte, E, Roth, S, Loukola, A, Bignell, G, Warren, W, Aminoff, M, Höglund, P, Järvinen, H, Kristo, P, Pelin, K, Ridanpää, M, Salovaara, R, Toro, T, Bodmer, W, Olschwang, S, Olsen, A, Stratton, MR, de la Chapelle, A, Aaltonen, L