| Genetic and physiological data implicating the new human gene G72 and the gene for d-amino acid oxidase in schizophrenia I Chumakov, M Blumenfeld, O Guerassimenko, L Cavarec, M Palicio, ... Proceedings of the National Academy of Sciences 99 (21), 13675-13680, 2002 | 1101 | 2002 |
| Duplication in chromosome 17p11. 2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a) P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, JE Hoogenduk, ... Neuromuscular disorders 1 (2), 93-97, 1991 | 744 | 1991 |
| The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication V Timmerman, E Nelis, W Van Hul, BW Nieuwenhuijsen, KL Chen, ... Nature genetics 1 (3), 171-175, 1992 | 454 | 1992 |
| Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis RHJ Houwen, S Baharloo, K Blankenship, P Raeymaekers, J Juyn, ... Nature genetics 8 (4), 380-386, 1994 | 408 | 1994 |
| Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families CV Broeckhoven, AM Genthe, A Vandenberghe, B Horsthemke, ... Nature 329 (6135), 153-155, 1987 | 365 | 1987 |
| A new gene (DYX3) for dyslexia is located on chromosome 2 T Fagerheim, P Raeymaekers, FE Tønnessen, M Pedersen, L Tranebjærg, ... Journal of medical genetics 36 (9), 664-669, 1999 | 296 | 1999 |
| Estimation of the size of the chromosome 17p11. 2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group. P Raeymaekers, V Timmerman, E Nelis, W Van Hul, P De Jonghe, ... Journal of medical genetics 29 (1), 5-11, 1992 | 140 | 1992 |
| APOE Genotype: No Influence on Galantamine Treatment Efficacy Nor on Rate of Decline in Alzheimer’s Disease J Aerssens, P Raeymaekers, S Lilienfeld, H Geerts, F Konings, W Parys Dementia and geriatric cognitive disorders 12 (2), 69-77, 2001 | 121 | 2001 |
| Association analysis of the 5‐HT2C receptor and 5‐HT transporter genes in bipolar disorder L Oruc, GR Verheyen, I Furac, M Jakovljević, S Ivezić, P Raeymaekers, ... American journal of medical genetics 74 (5), 504-506, 1997 | 103 | 1997 |
| CFTR haplotype backgrounds on normal and mutant CFTR genes H Cuppens, H Teng, P Raeymaekers, C De Boeck, JJ Casslman Human molecular genetics 3 (4), 607-614, 1994 | 96 | 1994 |
| Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I). P Raeymaekers, V Timmerman, P De Jonghe, L Swerts, J Gheuens, ... American journal of human genetics 45 (6), 953, 1989 | 91 | 1989 |
| Identification of a New Locus for Autosomal Dominant Non-Syndromic Hearing Impairment ( DFNA7 ) in a Large Norwegian Family T Fagerheim, Ø Nilssen, P Raeymaekers, V Brox, T Moum, HH Elverland, ... Human molecular genetics 5 (8), 1187-1191, 1996 | 87 | 1996 |
| Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11. 2-p12. V Timmerman, P Raeymaekers, P De Jonghe, G De Winter, L Swerts, ... American journal of human genetics 47 (4), 680, 1990 | 77 | 1990 |
| CAG repeat expansions in bipolar and unipolar disorders. L Oruc, K Lindblad, GR Verheyen, S Ahlberg, M Jakovljević, S Ivezić, ... American journal of human genetics 60 (3), 730, 1997 | 73 | 1997 |
| Assignment of X-linked hydrocephalus to Xq28 by linkage analysis PJ Willems, I Dijkstra, BJ Van der Auwera, L Vits, P Coucke, ... Genomics 8 (2), 367-370, 1990 | 68 | 1990 |
| A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorder I Massat, D Souery, O Lipp, S Blairy, G Papadimitriou, D Dikeos, ... American journal of medical genetics 96 (2), 136-140, 2000 | 67 | 2000 |
| Positive association between the GABRA5 gene and unipolar recurrent major depression L Oruč, GR Verheyen, IF Furač, S Ivezić, M Jakovljević, P Raeymaekers, ... Neuropsychobiology 36 (2), 62-64, 1997 | 53 | 1997 |
| Further localization of X-linked hydrocephalus in the chromosomal region Xq28 PJ Willems, L Vits, P Raeymaekers, J Beuten, P Coucke, JJA Holden, ... American journal of human genetics 51 (2), 307, 1992 | 53 | 1992 |
| Analysis of the tyrosine hydroxylase and dopamine D4 receptor genes in a Croatian sample of bipolar I and unipolar patients L Oruč, GR Verheyen, I Furač, M Jakovljević, S Ivezić, P Raeymaekers, ... American journal of medical genetics 74 (2), 176-178, 1997 | 50 | 1997 |
| Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree V Timmerman, P Raeymaekers, E Nelis, P De Jonghe, L Muylle, ... Journal of the neurological sciences 109 (1), 41-48, 1992 | 49 | 1992 |
