Hudson, G., Carelli, V., Horvath, R., Zeviani, M., Smeets, H.J.M., Chinnery, P.F. X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy. MOLECULAR VISION 2007 Dec;13:2339-43. IF: 2.377

Souren, N.Y.P., Paulussen, A.D.C., Loos, R.J., Gielen, M.J.F., Beunen, G., Fagard, R., Derom, C., Vlietinck, R., Zeegers, M.P.A. Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities. DIABETOLOGIA 2007 Oct;50(10):2107-16.
IF: 5.247

de Wit, L.E., Spruijt, L., Schoonderwoerd, G.C., de Coo, I.F., Smeets, H.J.M., Scholte, H.R., Sluiter, W. A simplified and reliable assay for complex I in human blood lymphocytes. JOURNAL OF IMMUNOLOGICAL METHODS 2007 Sep;326 (1-2):76-82. IF: 2.402
MEDICAL GENETICS 2007 Sep;44(9),562-569. IF: 5.087

Bergman, J.E., Veenstra-Knol, H.E., van Essen, A.J., van Ravenswaaij, C.M., den Dunnen, W.F., van den Wijngaard, A., van Tintelen, J.P.
Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene. European Journal of Medical Genetics 2007 Sep;50(5): 355-66. IF: 1.614

Moonen, R.M., Paulussen, A.D.C., Souren, N.Y.P., Kessels, A.G., Rubio-Gozalbo, M.E., Villamor, E. Carbamoyl phosphate synthetase polymorphisms as a risk factor for necrotizing enterocolitis. PEDIATRIC RESEARCH 2007 Aug;62(2):188-90. IF: 2.619

Smits, K.M., Smits, L.J.M., Peeters, F., Schouten, J., Janssen, R.J.H.L., Smeets, H.J.M., van Os, J.J., Prins, M.H.

The influence of 5-HTTLPR and STin2 polymorphisms in the serotonin transporter gene on treatment effect of selective serotonin reuptake inhibitors in depressive patients. Psychiatr Genet. 2008 Aug;18(4):184-90. IF:2.257

Hudson, G., Carelli, V., Spruijt, L., Gerards, M., Mowbray, C., Achilli, A., Pyle, A., Elson, J., Howell, N., La Morgia, C., Valentino, M.L., Huoponen, K., Savontaus, M.L., Nikoskelainen, E., Sadun, A.A., Salomao, S.R., Belfort R. Jr, Griffiths, P., Man, P.Y., de Coo, R.F., Horvath, R., Zeviani, M., Smeets, H.J.M., Torroni, A., Chinnery, P.F. Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background. AMERICAN JOURNAL OF HUMAN GENETICS 2007 Aug;81(2):228-33. IF: 12.629

Meex, S.J.R., van Greevenbroek, M.M.J.,
Ayoubi, T.A.Y., Vlietinck, R., van Vliet-Ostaptchouk, J.V., Hofker, M.H., Vermeulen, V.M.M.J., Schalkwijk, C.G., Feskens, E.J.M., Boer, J.M., Stehouwer, C.D.A., van der Kallen, C.J.H., de Bruin, T.W. Activating transcription factor 6 polymorphisms and haplotypes are associated with impaired glucose homeostasis and type 2 diabetes in Dutch Caucasians. JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 2007 Jul;92(7):2720-5. IF: 5.799

Saenen, J.B., Paulussen, A.D.C., Jongbloed, R.J.E., Marcelis, C.L., Gilissen, R.A., Aerssens, J., Snyders, D.J., Raes, A.L. A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY 2007 Jul;43(1):63-72. IF: 4.859

Spruijt, L., Smeets, H.J.M., Hendrickx, A., Bettink-Remeijer, M.W., Maat-Kievit, A., Schoonderwoerd, K.C., Sluiter, W., de Coo, I.F., Hintzen, R.Q. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
ARCHIVES OF NEUROLOGY 2007 Jun;64(6),890-3. IF: 5.204

Overeem, S., Schelhaas, H.J., Blijham, P.J., Grootscholten, M.I., ter Laak, H.J., Timmermans, J., van den Wijngaard, A., Zwarts, M.J. Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation. NEUROMUSCULAR DISORDERS 2007 Jun;17(6):490-3. IF: 2.615

Van Hooren, R., Van den Borne,  H.W., Curfs, L.M.G., Widdershoven, G.A.M. Ethics of prevention: an interactive computer tailored program. SCANDINAVIAN JOURNAL OF PUBLIC HEALTH 2007 May;35(5):503-509. IF: 1.021

Rombout-Sestrienkova E, Loots WJ, Van Deursen CT, Koek GH. Hereditaire hemochromatose. Nederlands Tijdschrift voor Hematologie 2007;4:89-97. IF:  -

Blok, M.J., Spruijt, L., de Coo, I.F., Schoonderwoerd, K., Hendrickx, A., Smeets, H.J.M.
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease. JOURNAL OF MEDICAL GENETICS. 2007 Apr;44(4):e74-e74. IF: 5.087

Volders, P.G.A., Zhu, Q., Timmermans, C.C.M.M., Eurlings, P.M., Su, X., Arens, Y.H.J.M., Li, L., Jongbloed, R.J.E., Xia, M., Rodriguez, L.M., Chen, Y.H. Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21. HEART RHYTHM 2007 Apr;4(4):469-475. IF: 3.777

Hofman N, Postema PG, van Langen IM, Nannenberg EA, Alders M, Jongbloed R, Smeets HJ, Wilde AA. Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years. Ned Tijdschr Geneeskd. 2007 Mar 17;151(11):644-8. Dutch. SCI 1.548

Jacobs, L., Gerards, M., Chinnery, P., Dumoulin, J.C.M., de Coo, I., Geraedts, J.P.M., Smeets, H.J.M. mtDNA point mutations are present at various levels of heteroplasmy in human oocytes. MOLECULAR HUMAN REPRODUCTION 2007 Mar;13(3):149-54. IF: 2.76

Vydt, T.C.B., de Coo, R.F.M., Soliman, O.L.L., ten Cate, F.J., van Geuns, R.J.M., Vletter, W.B., Schoonderwoerd, K., van den Bosch, B.J.C., Smeets, H.J.M., Geleijnse, M.L. Cardiac involvement in adults with m.3243A>G MELAS mutation. AMERICAN JOURNAL OF CARDIOLOGY 2007 Jan;99(2):264-269. IF: 3.015

van den Wildenberg, E., Wiers, R.W.H.J., Dessers, J., Janssen, R.G., Lambrichs, E.H., Smeets, H.J.M., van Breukelen, G.J.P. A functional polymorphism of the mu-opioid receptor gene (OPRM1) influences cue-induced craving for alcohol in male heavy drinkers. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH 2007 Jan;31(1),10-2008. IF: 2.933

Kellen, E., Zeegers, M.P.A., Paulussen, A.D.C., Vlietinck, R.F.M., Vlem, E.V., Veulemans, H., Buntinx, F.J.V.M. Does occupational exposure to PAHs, diesel and aromatic amines interact with smoking and metabolic genetic polymorphisms to increase the risk on bladder cancer?; The Belgian case control study on bladder cancer risk. CANCER LETTERS 2007 Jan;245(1-2):51-60. IF: 3.277