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books | meeting abstracts | book chapters
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1998

1. Ahmad W, Brancolini V, Faiyaz ul Haque M, Lam H, ul Haque S, Haider M, Maimon A, Aita VM, Owen J, Brown D, Zegarelli DJ, Ahmad M, Ott J, Christiano AM (1998),
   "A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q121" (letters to the editor),
   American Journal of Human Genetics, 62(4):987-991
   [ full text (PDF) ]

2. Wasim Ahmad, Muhammad Faiyaz ul Haque, V Brancolini, Hui C Tsou, Sayed ul Haque, HaMut Lam, Vincent M Aita, Jason Owen, Michelle deBlaquiere, Jorge Frank, Peter B Cserhalmi-Friedman, Andrew Leask, John A McGrath, Monica Peacocke, Mahmud Ahmad, J Ott, Angela M Christiano (1998)
   "Alopecia universalis associated with a mutation in the human hairless gene",
   Science , 279 (5351), 720-724.
   [abstract] [Medline entry]

3. Apaydin F, Pfister M, Iber M, Kandogan T, Leal SM, Brandle U, Cura O, Zenner HP (1998),
   "Hereditary deafness in Turkey. Initial results" (in German),
   HNO, 46(9):809-814.
   [ Medline entry]

4. M Arcos-Burgos, LG Palacio, I Jimenez, N Pineda, O Mora, JL Sanchez, M Jimenez, A Munoz, V Brancolini, M Devoto, A Ruiz-Linares (1998),
   "Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration Simulations of power for the detection of genetic linking" (in Spanish),
   Review of Neurologia, 26(149):50-52.
   [ Medline entry]

5. P Banerjee, PW Kleyn, JA Knowles, CA Lewis, BM Ross, E Parano, SG Kovats, JJ Lee, GK Penchaszadeh, J Ott, SG Jacobson, TC Gilliam (1998)
   "TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa",
   Nature Genetics, 18(2):177-179.
   [ abstract] [ Medline entry]

6. P Banerjee, CA Lewis, PW Kleyn, YY Shugart, BM Ross, GK Penchaszadeh, J Ott , SG Jacobson, TC Gilliam, JA Knowles (1998),
   "Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p213",
   Genomics, 48(2):171-177.
   [abstract] [ Medline entry] [ full text (PDF)]

7. Jane F. Bleasel, Daniel Holderbaum, Valeria Brancolini, Roland W. Moskowitz, Eileen L. Considine, Darwin J. Prockop, Marcella Devoto, Charlene J. Williams (1998),
   "Five families with arginine519-cysteine mutation in COL2A1: Evidence for three distinct founders",
   Human Mutation, 12(3), 172-176.
   [abstract] [ Medline entry]

8. C Bond, KS Laforge, M Tian, D Melia, S Zhang, L Borg, J Gong, J Schluger, JA Strong, SM Leal, JA Tischfield, MJ Kreek, L Yu (1998),
   "Variation in receptor function from a single nucleotide polymorphism in the human mu opioid receptor gene: possible implications for opioid addiction",
   Proceedings of National Academy of Sciences (USA), 95:9608-9613.
   [ Medline entry] [ full text (PDF)]

9. Brown DM, Matise TC, Koike G, Simon JS, Winer ES, Zangen S, McLaughlin MG, Shiozawa M, Atkinson OS, Hudson JR Jr, Chakravarti A, Lander ES, Jacob HJ (1998)
   "An integrated genetic linkage map of the laboratory rat",
   Mammalian Genome, 9(7):521-530.
   [ Medline entry]

10. C Robert Cloninger, Charles A Kaufmann, Stephen V Faraone, Dolores Malaspina, Dragan M Svrakic, Jill Harkavy-Friedman, Brian K Suarez, Tara C Matise, David Shore, Hang Lee, Carol L Hampe, Debra Wynne, Caroline Drain, Paul D Markel, Christopher T Zambuto, Karin Schmitt, Ming T Tsuang (1998),
    "Genome-wide search for schizophrenia susceptibility loci: The NIMH genetics initiative and millennium consortium",
    American Journal of Medical Genetics, 81(4):275-281.
    [ Medline entry]

11. M Devoto, K Shimoya, J Caminis, J Ott, A Tenenhouse, MP Whyte, L Sereda, S Hall, E Considine, CJ Williams, G Tromp, H Kuivaniemi, L Ala-Kokko, DJ Prockop, LD Spotila (1998),
    "First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q",
    European Journal of Human Genetics, 6:151-157.
    [ Medline entry]

12. Stephen V Faraone, Tara Matise, Dragan Svrakic, John Pepple, Dolores Malaspina, Brian Suarez, Carol Hampe, Christopher T Zambuto, Karin Schmitt, Joanne Meyer, Paul Markel, Hang Lee, Jill Harkavy-Friedman, Charles Kaufmann, C Robert Cloninger, Ming T Tsuang (1998),
    "Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium",
    American Journal of Medical Genetics, 81(4):290-295.
    [ Medline entry]

13. A Gambardella, A Bolino, M Muglia, P Valentino, F Bono, RL Oliveri, M Sabatelli, V Brancolini, C Van Broeckhoven, G Romeo, M Devoto , A Quattrone (1998),
    "Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)",
    Neurology, 50(3):799-801
    [Medline entry]

14. Linn Gieser, Ricardo Fujita, Harald H Goring, Jurg Ott, Dennis R. Hoffman, Artur V. Cideciyan,, David G. Birch, Samuel G. Jacobson, and Anand Swaroop (1998),
    "A Novel Locus (RP24) for X-linked Retinitis Pigmentosa Maps to Xq26-27",
    American Journal of Human Genetics, 63(5):1439-1447.
    [ Medline entry] [ full text (PDF) ]

15. SC Heath (1998)
    "Generating consistent genotypic configurations for multi-allelic loci and large complex pedigrees",
    Human Heredity, 48:1-11.
    [abstract] [ Medline entry]

16. JJ Higgins, I Litvan, LT Pho, W Li, LE Nee (1998)
    "Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene",
    Neurology, 50(1): 270-273.
    [ Medline entry ]

17. SH Juo, TH Beaty, J Xu, VL Prenger, J Coresh, PO Kwiterovich Jr (1998)
    "Segregation analysis of two-Locus models regulating Apolipoprotein-AI levels",
    Genetic Epidemiology, 15(1): 73-86.
    [ abstract] [ Medline entry]

18. SH Juo , SJH Bredie, LA Kiemeney, PNM Demacker, AFH Stalenhoef (1998),
    "A common genetic Mechanism determine plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia",
    American Journal of Human Genetics, 63(2):586-594.
    [abstract] [ Medline entry] [ full text (PDF) ]

19. Kaufmann CA, Suarez B, Malaspina D, Pepple J, Svrakic D, Markel PD, Meyer J, Zambuto CT, Schmitt K, Matise TC, Harkavy Friedman JM, Hampe C, Lee H, Shore D, Wynne D, Faraone SV, Tsuang MT, Cloninger CR (1998)
    "NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigree",
    American Journal of Medical Genetics, 81(4):282-289.
    [ Medline entry]

20. James A Knowles, Peter A Rao, Tara Cox-Matise, Jo Ellen Loth, Gracielle M de Jesus, Laura Levine, Kamna Das, Graciela K Penchaszadeh, Joyce R Alexander, Bernard Lerer, Jean Endicott, Jurg Ott, T Conrad Gilliam, and Miron Baron (1998),
    "No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees",
    American Journal of Human Genetics, 62, 916-924
    [abstract] [Medline entry] [ full text (PDF) ]

21. SM Leal, F Apaydin, C Barnwell, M Iber, T Kandogan, M Pfister, U Braendle, O Cura, M Schwalb, H-P Zenner, E Vitale (1998),
    "A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregations DFNB9",
    European Journal of Human Genetics, 6:341-344.
    [ Medline entry]

22. A Lernmark, J Ott (1998),
    "Sometimes it's hot, sometimes it's not" (News & Views),
    Nature Genetics, 19(3):213-214.

23. W Li (1998)
    Comments on "Simplicity and complexity in gene evolution" (Letters to the Editor),
    Complexity, 3(5):10.

24. W Li, CSJ Fann, J Ott (1998),
    "Low order polynomial trends of female-to-male map distance ratios along human chromosomes",
    Human Heredity, 48(5), 266-270.
    [abstract] [ Medline entry]

25. W Li , G Stolovitzky, P Bernaola-Galvan, JL Oliver (1998),
    "Compositional heterogeneity within, and uniformity between, DNA sequences of yeast chromosomes",
    Genome Research, 8(9): 916-928.
    [abstract] [Medline entry] [ full text (PDF) ] [ full text (Postscript) ]

26. Paul Lucek, Jens Hanke, Jens Reich, Sara A Solla, Jurg Ott (1998),
    "Multi-locus nonparametric linkage analysis of complex trait loci with neural networks",
    Human Heredity, 48(5), 266-270.
    [abstract] [ Medline entry]

27. Martina Plasilova, Eva Ferakova, Ludovit Kadasi, Helena Polakova, Anton Gerinec, Jurg Ott, Vladimir Ferak (1998),
    "Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from Slovakia",
    Human Heredity, 48(1):30-33.
    [ Medline entry]

28. I Simonic, GS Gericke, J Ott, JL Weber (1998),
    "Identification of genetic markers associated with Gilles de la Tourette Syndrome in an Afrikaner population",
    American Journal of Human Genetics, 63(3):839-884.
    [abstract] [ Medline entry] [ full text (PDF)]