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1. Rizzu, P; Joosse, M; Ravid, R; Hoogeveen, A; Kamphorst, W; van Swieten, JC; Willemsen, R; Heutink, P
   Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients
   HUMAN MOLECULAR GENETICS
   
   P. Rizzu et al., "Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients", HUM MOL GEN, 9(20), 2000, pp. 3075-3082
2. Froelich, S; Houlden, H; Rizzu, P; Chakraverty, S; Baker, M; Kwon, J; Nowotny, P; Isaacs, A; Nowotny, V; Wauters, E; van Baren, MJ; Oostra, BA; Hardy, J; Lannfelt, L; Goate, A; Hutton, M; Lendon, CL; Heutink, P
   Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21
   GENOMICS
   
   S. Froelich et al., "Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21", GENOMICS, 60(2), 1999, pp. 129-136
3. van Swieten, JC; Stevens, M; Rosso, SM; Rizzu, P; Joosse, M; de Koning, I; Kamphorst, W; Ravid, R; Spillantini, MG; Niermeijer, MF; Heutink, P
   Phenotypic variation in hereditary frontotemporal dementia with tau mutations
   ANNALS OF NEUROLOGY
   
   J.C. van Swieten et al., "Phenotypic variation in hereditary frontotemporal dementia with tau mutations", ANN NEUROL, 46(4), 1999, pp. 617-626
4. Bonifati, V; Joosse, M; Nicholl, DJ; Vanacore, N; Bennett, P; Rizzu, P; Fabbrini, G; Marconi, R; Colosimo, C; Locuratolo, N; Stocchi, F; Bonuccelli, U; De Mari, M; Wenning, G; Vieregge, P; Oostra, B; Meco, G; Heutink, P
   The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronicvariant of the disease-associated H1 haplotype in Italian cases
   NEUROSCIENCE LETTERS
   
   V. Bonifati et al., "The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronicvariant of the disease-associated H1 haplotype in Italian cases", NEUROSCI L, 274(1), 1999, pp. 61-65
5. Houlden, H; Rizzu, P; Stevens, M; de Knijff, P; van Duijn, CM; van Swieten, JC; Heutink, P; Perez-Tur, J; Thomas, V; Baker, M; Morris, H; Rossor, M; Jannsen, JC; Petersen, RC; Dodd, P; Dark, F; Boeve, B; Dickson, D; Davies, P; Pickering-Brown, S; Mann, D; Adamson, J; Lynch, T; Payami, H; Poorkaj, P; Bird, TD; Schellenberg, GD; Chakraverty, S; Norton, J; Morris, JC; Goate, A; Hutton, M; Hardy, J
   Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations
   NEUROSCIENCE LETTERS
   
   H. Houlden et al., "Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations", NEUROSCI L, 260(3), 1999, pp. 193-195
6. Rizzu, P; Van Swieten, JC; Joosse, M; Hasegawa, M; Stevens, M; Tibben, A; Niermeijer, MF; Hillebrand, M; Ravid, R; Oostra, BA; Goedert, M; van Duijn, CM; Heutink, P
   High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   P. Rizzu et al., "High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands", AM J HU GEN, 64(2), 1999, pp. 414-421
7. HUTTON M; LENDON CL; RIZZU P; BAKER M; FROELICH S; HOULDEN H; PICKERINGBROWN S; CHAKRAVERTY S; ISAACS A; GROVER A; HACKETT J; ADAMSON J; LINCOLN S; DICKSON D; DAVIES P; PETERSEN RC; STEVENS M; DEGRAAFF E; WAUTERS E; VANBAREN J; HILLEBRAND M; JOOSSE M; KWON JM; NOWOTNY P; CHE LK; NORTON J; MORRIS JC; REED LA; TROJANOWSKI J; BASUN H; LANNFELT L; NEYSTAT M; FAHN S; DARK F; TANNENBERG T; DODD PR; HAYWARD N; KWOK JBJ; SCHOFIELD PR; ANDREADIS A; SNOWDEN J; CRAUFURD D; NEARY D; OWEN F; OOSTRA BA; HARDY J; GOATE A; VANSWIETEN J; MANN D; LYNCH T; HEUTINK P
   ASSOCIATION OF MISSENSE AND 5'-SPLICE-SITE MUTATIONS IN TAU WITH THE INHERITED DEMENTIA FTDP-17
   Nature
   
   M. Hutton et al., "ASSOCIATION OF MISSENSE AND 5'-SPLICE-SITE MUTATIONS IN TAU WITH THE INHERITED DEMENTIA FTDP-17", Nature, 393(6686), 1998, pp. 702-705
8. HEUTINK P; STEVENS M; RIZZU P; BAKKER E; KROS JM; TIBBEN A; NIERMEIJER MF; VANDUIJN CM; OOSTRA BA; VANSWIETEN JC
   HEREDITARY FRONTOTEMPORAL DEMENTIA IS LINKED TO CHROMOSOME-17Q21-Q22 - A GENETIC AND CLINICOPATHOLOGICAL STUDY OF 3 DUTCH FAMILIES
   Annals of neurology
   
   P. Heutink et al., "HEREDITARY FRONTOTEMPORAL DEMENTIA IS LINKED TO CHROMOSOME-17Q21-Q22 - A GENETIC AND CLINICOPATHOLOGICAL STUDY OF 3 DUTCH FAMILIES", Annals of neurology, 41(2), 1997, pp. 150-159
9. RIZZU P; HADDAD BR; VALLCORBA I; ALONSO A; FERRO MT; GARCIASAGREDO JM; BALDINI A
   DELINEATION OF A DUPLICATION MAP OF CHROMOSOME 3Q - A NEW CASE CONFIRMS THE EXCLUSION OF 3Q25-Q26.2 FROM THE DUPLICATION 3Q SYNDROME CRITICAL REGION
   American journal of medical genetics
   
   P. Rizzu et al., "DELINEATION OF A DUPLICATION MAP OF CHROMOSOME 3Q - A NEW CASE CONFIRMS THE EXCLUSION OF 3Q25-Q26.2 FROM THE DUPLICATION 3Q SYNDROME CRITICAL REGION", American journal of medical genetics, 68(4), 1997, pp. 428-432
10. RIZZU P; LINDSAY EA; TAYLOR C; ODONNELL H; LEVY A; SCAMBLER P; BALDINI A
    CLONING AND COMPARATIVE MAPPING OF A GENE FROM THE COMMONLY DELETED REGION OF DIGEORGE AND VELOCARDIOFACIAL SYNDROMES CONSERVED IN C-ELEGANS
    Mammalian genome
    
    P. Rizzu et al., "CLONING AND COMPARATIVE MAPPING OF A GENE FROM THE COMMONLY DELETED REGION OF DIGEORGE AND VELOCARDIOFACIAL SYNDROMES CONSERVED IN C-ELEGANS", Mammalian genome, 7(9), 1996, pp. 639-643
11. LINDSAY EA; RIZZU P; ANTONACCI R; JURECIC V; DELMASMATA J; LEE CC; KIM UJ; SCAMBLER PJ; BALDINI A
    A TRANSCRIPTION MAP IN THE CATCH22 CRITICAL REGION - IDENTIFICATION, MAPPING, AND ORDERING OF 4 NOVEL TRANSCRIPTS EXPRESSED IN HEART
    Genomics
    
    E.A. Lindsay et al., "A TRANSCRIPTION MAP IN THE CATCH22 CRITICAL REGION - IDENTIFICATION, MAPPING, AND ORDERING OF 4 NOVEL TRANSCRIPTS EXPRESSED IN HEART", Genomics, 32(1), 1996, pp. 104-112
12. HADDAD B; ANTONACCI R; RIZZU P; LINDSAY EA; HUGHES MR; SMITH LC; KNAPP RD; BALDINI A
    MAPPING SEGMENTAL IMBALANCES USING COMPARATIVE GENOMIC HYBRIDIZATION AND EIGENANALYSIS
    Cytogenetics and cell genetics
    
    B. Haddad et al., "MAPPING SEGMENTAL IMBALANCES USING COMPARATIVE GENOMIC HYBRIDIZATION AND EIGENANALYSIS", Cytogenetics and cell genetics, 71(3), 1995, pp. 276-279
13. RIZZU P; BALDINI A
    3 MEMBERS OF THE HUMAN CYSTATIN GENE SUPERFAMILY, AHSG, HRG, AND KNG,MAP WITHIN ONE MEGABASE OF GENOMIC DNA AT 3Q27
    Cytogenetics and cell genetics
    
    P. Rizzu e A. Baldini, "3 MEMBERS OF THE HUMAN CYSTATIN GENE SUPERFAMILY, AHSG, HRG, AND KNG,MAP WITHIN ONE MEGABASE OF GENOMIC DNA AT 3Q27", Cytogenetics and cell genetics, 70(1-2), 1995, pp. 26-28
14. AQUA MS; RIZZU P; LINDSAY EA; SHAFFER LG; ZACKAI EH; OVERHAUSER J; BALDINI A
    DUPLICATION 3Q SYNDROME - MOLECULAR DELINEATION OF THE CRITICAL REGION
    American journal of medical genetics
    
    M.S. Aqua et al., "DUPLICATION 3Q SYNDROME - MOLECULAR DELINEATION OF THE CRITICAL REGION", American journal of medical genetics, 55(1), 1995, pp. 33-37
15. LINDSAY EA; RIZZU P; ANTONACCI R; JURECIC V; DELMASMATA J; KIM UJ; SCAMBLER P; BALDINI A
    VELO-CARDIO-FACIAL SYNDROME AND CATCH22 - 5 DISTINCT TRANSCRIPTS EXPRESSED IN HEART IDENTIFIED, MAPPED AND ORDERED IN THE CRITICAL REGION
    American journal of human genetics
    
    E.A. Lindsay et al., "VELO-CARDIO-FACIAL SYNDROME AND CATCH22 - 5 DISTINCT TRANSCRIPTS EXPRESSED IN HEART IDENTIFIED, MAPPED AND ORDERED IN THE CRITICAL REGION", American journal of human genetics, 57(4), 1995, pp. 150-150
16. RIZZU P; OVERHAUSER J; JACKSON LG; BALDINI A
    CORNELIA-DELANGE-SYNDROME - TOWARD THE POSITIONAL CLONING OF A LOCUS AT 3Q27
    American journal of human genetics
    
    P. Rizzu et al., "CORNELIA-DELANGE-SYNDROME - TOWARD THE POSITIONAL CLONING OF A LOCUS AT 3Q27", American journal of human genetics, 57(4), 1995, pp. 1938-1938
17. RIZZU P; BALDINI A
    SUBCHROMOSOMAL BAND INTERVAL MAPPING AND ORDERING OF DNA MARKERS IN THE REGION 3Q26.3-Q27 INVOLVED IN THE DUP(3Q) SYNDROME
    Genomics
    
    P. Rizzu e A. Baldini, "SUBCHROMOSOMAL BAND INTERVAL MAPPING AND ORDERING OF DNA MARKERS IN THE REGION 3Q26.3-Q27 INVOLVED IN THE DUP(3Q) SYNDROME", Genomics, 24(3), 1994, pp. 580-582
18. TOLA S; RIZZU P; LEORI G
    A SPECIES-SPECIFIC DNA-PROBE FOR THE DETECTION OF MYCOPLASMA-AGALACTIAE
    Veterinary microbiology
    
    S. Tola et al., "A SPECIES-SPECIFIC DNA-PROBE FOR THE DETECTION OF MYCOPLASMA-AGALACTIAE", Veterinary microbiology, 41(4), 1994, pp. 355-361
19. MURESU R; RUBINO S; RIZZU P; BALDINI A; COLOMBO M; CAPPUCCINELLI P
    A NEW METHOD FOR IDENTIFICATION OF TRICHOMONAS-VAGINALIS BY FLUORESCENT DNA IN-SITU HYBRIDIZATION
    Journal of clinical microbiology
    
    R. Muresu et al., "A NEW METHOD FOR IDENTIFICATION OF TRICHOMONAS-VAGINALIS BY FLUORESCENT DNA IN-SITU HYBRIDIZATION", Journal of clinical microbiology, 32(4), 1994, pp. 1018-1022
20. RUBINO S; LEORI G; RIZZU P; ERRE G; COLOMBO MM; UZZAU S; MASALA G; CAPPUCCINELLI P
    TNPHOA SALMONELLA-ABORTUSOVIS MUTANTS UNABLE TO ADHERE TO EPITHELIAL-CELLS AND WITH REDUCED VIRULENCE IN MICE
    Infection and immunity
    
    S. Rubino et al., "TNPHOA SALMONELLA-ABORTUSOVIS MUTANTS UNABLE TO ADHERE TO EPITHELIAL-CELLS AND WITH REDUCED VIRULENCE IN MICE", Infection and immunity, 61(5), 1993, pp. 1786-1792