publications (journal article)

books | meeting abstracts | book chapters
Rockefeller: 2007 | 2006 | 2005 | 2004 | 2003 | 2002 | 2001 | 2000 | 1999 | 1998 | 1997 | 1996
Columbia: 1995 | 1994 | 1993 | 1992 | 1991 | 1990 | 1989 | 1988
1987 | 1986 | 1985 | 1984 | 1983 | 1982 | 1981 | 1980 | 1979 | 1978 | 1977 | 1976 | 1975 | 1974

+ 1996

  1. A Auricchio, V Brancolini, G Casari, PJ Milla, VV Smith, M Devoto, A Ballabio (1996),
    "The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28",
    American Journal of Human Genetics, 58, 743-748
    [Medline entry]

  2. V Barone, D Weber, Y Luo, V Brancolini, M Devoto, G Romeo (1996),
    "Exclusion of linkage between RET and neuronal intestinal Dysplasia type B",
    American Journal of Medical Genetics, 62(2), 195-198.
    [abstract] [Medline entry]

  3. A Bolino, V Brancolini , F Bono, A Bruni, A Gambardella, G Romeo, A Quattrone, M Devoto (1996),
    "Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheats to chromosome 11q23 by homozygosity mapping and haplotype sharing",
    Human Molecular Genetics, 5(7), 1051-1054.
    [abstract] [Medline entry]

  4. V Brancolini, M Devoto (1996)
    "Genetic linkage studies for the identification of cancer-related genes",
    Ann Ist Super Sanita, 32(1):173-180
    [ Medline entry]

  5. CSJ Fann, V Brancolini (1996),
    "A new version of Cyrillic: overview" (Software Review),
    European Journal of Human Genetics, 4(3), 188

  6. R Fujita, E Bingham, P Forsythe, C McHenry V Aita, BA Navia, K Dry, M Segal, M Devoto , G Bruns, AF Wright, J Ott , PA Sieving, and A Swaroop (1996),
    "A recombination outside the BB deletion refines the location of the X-linked retinitis pigmentosa locus RP3",
    American Journal of Human Genetics 59, 152-158
    [ Medline entry]

  7. Edward I Ginns, Jurg Ott, Janice A Egeland, Cleona R Allen, Cathy SJ Fann, David L Pauls, Jean Weissenbach, John P Carulli, Kathleen M Falls, Tim P Keith, and Steven M Paul (1996),
    "A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish",
    Nature Genetics, 12(4), 431-435.
    [abstract]

  8. Levinson DF, Wildenauer DB, Schwab SG, Albus M, Hallmayer J, Lerer B, Maier W, Blackwood D, Muir W, St Clair D, Morris S, Moises HW, Yang L, Kristbjarnarson H, Helgason T, Wiese C, Collier DA, Holmans P, Daniels J, Rees M, Asherson P, Roberts Q, Cardno A, Arranz MJ, Vallada H, McGuffin D, Owen MJ, Pulver AE, Antonarakis SE, Babb R, Blouin JL, DeMarchi N, Dombroski B, Housman D, Karayiorgou M, Ott J, Kasch L, Kazazian H, Lasseter VK, Loetscher E, Luebbert H, Nestadt G, Ton C, Wolyniec PS, Laurent C, de Chaldee M, Thibaut F, Jay M, Samolyk D, Petit M, Campion D, Mallet J, Straub RE, MacLean CJ, Easter SM, O'Neill FA, Walsh D, Kendler KS, Gejman PV, Cao QH, Gershon E, Badner J, Beshah E, Zhang J, Riley BP, Rajagopalan S, Mogudi-Carter M, Jenkins T, Williamson R, DeLisi LE, Garner C, Kelly M, LeDuc C, Cardon L, Lichter J, Harris T, Loftus J, Shields G, Comasi M, Vita A, Smith A, Dann J, Joslyn G, Gurling H, Kalsi G, Brynjolfsson J, Curtis D, Sigmundsson T, Butler R (1997)
    "Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study",
    American Journal of Medical Genetics, 67(6), 580-594

  9. C Merette, J Ott (1996),
    "Estimating parental relationship in linkage analysis of recessive traits",
    American Journal of Medical Genetics, 63, 386-391

  10. J Ott (1996),
    "Complex traits on the map" (news and views),
    Nature, 379, 772-773

  11. David L Pauls , Jurg Ott, Steven M Paul, Cleona R Allen, Cathy S J Fann, John P Carulli, Kathleen M Falls, Christine A Bouthillier, Thomas C Gravius, Tim P Keith, Janice A Egeland, and Edward I Ginns (1996),
    "Chromosome 18 markers: Linked or not linked to bipolar affective disorders in the old order Amish? A reply to Gershon et al",
    American Journal of Human Genetics, 58(6), 1384-1385

  12. S Ranta, A-E Lehesjoki, A Hirvasniemi, J Weissenbach, B Ross, H Riethman, SM Leal , A de la Chapelle, TC Gilliam (1996)
    "Genetic and physical mapping of the progressive epilepsy with mental retardation (EMPR) gene on chromosome 8p",
    Genome Research, 6(5), 351-360.
    [abstrasct]

  13. G D Schuler, M S Boguski, E A Stewart, L D Stein, G Gyapay, K Rice, R E White, P Rodriguez-Tomé, A Aggarwal, E Bajorek, S Bentolila, B B Birren, A Butler, A B Castle, N Chiannilkulchai, A Chu, C Clee, S Cowles, P J R Day, T Dibling, N Drouot, I Dunham, S Duprat, C East, C Edwards, J-B Fan, N Fang, C Fizames, C Garrett, L Green, D Hadley, M Harris, P Harrison, S Brady, A Hicks, E Holloway, L Hui, S Hussain, C Louis-Dit-Sully, J Ma, A MacGilvery, C Mader, A Maratukulam, T C Matise, K B McKusick, J Morissette, A Mungall, D Muselet, H C Nusbaum, D C Page, A Peck, S Perkins, M Piercy, F Qin, J Quackenbush, S Ranby, T Reif, S Rozen, C Sanders, X She, J Silva, D K Slonim, C Soderlund, W-L Sun, P Tabar, T Thangarajah, N Vega-Czarny, D Vollrath, S Voyticky, T Wilmer, X Wu, M D Adams, C Auffray, N A R Walter, R Brandon, A Dehejia, P N Goodfellow, R Houlgatte, J R Hudson Jr, S E Ide, K R Iorio, W Y Lee, N Seki, T Nagase, K Ishikawa, N Nomura, C Phillips, M H Polymeropoulos, M Sandusky, K Schmitt, R Berry, K Swanson, R Torres, J C Venter, J M Sikela, J S Beckmann, J Weissenbach, R M Myers, D R Cox, M R James, D Bentley, P Deloukas, E S Lander, T J Hudson (1996),
    A gene map of the human genome ,
    Science, 274, 540-546
    [ Medline entry]

  14. H Schuster, TF Wienker, S Bahring, N Bilginturan, HR Toka, H Neitzel, E Jeschke, O Toka, D Gilbert, A Lowe, J Ott , H Haller, FC Luft (1996),
    "Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12",
    Nature Genetics, 13, 98-100

  15. I Simonic, J Ott , (1996)
    "Novel etiological hypotheses imply new analysis methods for schizophrenia genetics",
    Schizophrenia Research, 20, 235-237

  16. LD Spotila, J Caminis, M Devoto , K Shimoya, L Sereda, J Ott, MP Whyte, A Tenenhouse, DJ Prockop (1996),
    "Osteopenia in 37 members of seven families: Analysis based on a model of dominant inheritance",
    Molecular Medicine 2, 313-324

  17. Anne C Walsh, W Li, Daniel R Rosen, David A Lawrence (1996),
    "Genetic mapping of GLCLC, the human gene encoding the catalytic subunit of gamma-glutamylcysteine synthetase, to chromosome 6p12 and characterization of a polymorphic trinucleotide repeat within its 5' untranslated region",
    Cytogenetics and Cell Genetics , 75(1):14-16
    [ Medline entry]

  18. A Weith, G Brodeur, G Bruns, T Matise, D Mischke, D Nizetic, M Seldin, N van Roy, J Vance (1996),
    "Report of the second international workshop on human chromosome1 mapping 1995",
    Cytogenetics and Cell Genetics, 72:113-154.
    [ abstract]

  19. The Schizophrenia Linkage Collaborative Groups for Chromosomes 3, 6, and 8 ( ... TC Matise ... ) (1996)
    "Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study",
    American Journal of Medical Genetics, 67: 580-594

  20. D Warburton, SH Shaw, TC Matise , S Kalachikov, S Fischer (1996),
    "Report of the third international workshop on human chromosome 13 mapping",
    Cytogenetics & Cell Genetics, 75(2-3):85-104