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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
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2001 Annual Meeting of American Society of Human Genetics (October 12-16, 2001, San Diego, CA)

1. Gordon D, Heath SC, Liu X, Ott J,
   "A transmission disequilibrium test that allows for genotyping errors in the analysis of single nucleotide polymorphism data",
   AJHG, 69(4):507.

2. Han Z, Li W, Shmulewitz D, Heath S, Auerbach S, Blundell M, Lehner T, Ott J, Stoffel M, Friedman JM, Breslow JL
   "Family based association study (qTDT) on lipid abnormality- candidate genes on an isolated, admixtured population",
   AJHG, 69(4):572

3. Majewski J, Li H, Ott J
   "The Ising model in physics and statistical genetics",
   AJHG, 69(4):525

4. Martinez-Mir A, Gordon D, Horev L, Ott J, Zlotogorski A, Christiano AM
   "Multiple cutaneous leiomyoma and uterine fibroids: Confirmation and refinement of the MCUL1locus",
   AJHG, 69(4):626.

5. Wessman M, Kallela M, Oswell G, Kaunisto M, Hartiala J, Broas P, Hamalainen E, Marttila P, Hiekkalinna T, Joslyn G, Papp J, Leal SM, Cantor R, Sobel E, Ott J, Havanka H, Farkkila M, Peltonen L, Palotie A,
   "A genome-wide scan identifies a genetic locus for migraine with aura",
   AJMG, 69(4):213

Genetic Analysis Workshop 12, San Antonio, Texas (2000)

1. CH Chen, SK Nath, SJ Finch, NR Mendell, D Gordon , RC Elston
   "A filter method based on sample prevalence for maximizing HLOD scores over genetic models"

2. D Gordon , SJ Finch, J Majewski, M Levenstien, J Edinton, J Ott
   "How many genomic regions should be followed up for linkage and association analyses of a complex trait?"

3. J Hoh, D Gordon, J Ott
   "Evaluation of scan statistics in their search for major genes"

4. W Li, D Nyholt
   "Marker selection by Akaike and Bayesian information criterion"

5. J Majewski, J Ott
   Usefulness of unaffected pedigree members in non-parametric linkage analysis

6. D Nyholt
   "Meta-analysis of genome-wide linkage scans"

7. A Wille, SM Leal
   "Can stepwise resampling improve the ability to detect multiple genes that influence quantitative traits?"

2001 Annual Meeting of American Society of Human Genetics (2001, San Diego, CA)

2000 Annual Meeting of American Society of Human Genetics (October 3-7, 2000, Philadelphia, PA)

1. L Baala, S Hadj-Rabia, D Hamel-Teillac, SM Leal , A Sefiani, Y de Prost, A Munnich, S Lyonnet, P Vabres
   "Homozygosity mapping of a locus for a novel form of syndromic ichthyosis to chromosome 3q27-q28".
   AJHG,s67, #674.

2. Z Han, SC Heath, D Shmulewitz, SB Auerbach, ML Blundell, T Lehner, J Ott , M Stoffel, JM Friedman, JL Breslow
   "Family based association study of candidate genes regulating lipid and apolipoprotein levels on the island of Kosrae",
   AJHG,s67, #1960

3. VE Kimonis, MJ Kovach, S Leal, B Waggoner, R Khardori, D Gelber
   "Clinic and molecular studies in a large unique family with Limb-Girdle Muscular Dystrophy and Paget disease of bone",
   AJHG,s67, #669.

4. S Kmoch, B Stiburkova, L Ondrova, M Zikanova, I Sebesta, J Majewski, J Ott
   "A primary transcript map for the familial Juvenile Hyperuricemic Nephropathy (FJHN) critical region on chromosome 16p11.2"
   AJHG,s67, #1436.

5. MJ Kovach, VE Kimonis, S Leal, B Waggoner, A Salam, R Khadori, D Gelber,
   "The gene for autosomal dominant Limb-Girdle Muscular Dystrophy and Paget disease of bone in a large family maps to a unique locus on 9p22.3-q12",
   AJHG,s67, #1794.

6. MH Lee, K Lu, D Gordon, J Ott, H Kojima, PO Kwiterowich, MJ Brownstein, G Salen, L Ose, T Mietinnen, R Pegoraro, H Hidaka, N Sakuma, A Pandya, S Patel
   "Fine-mapping and genetic analyses of Sitosterolemia: founder effects in at least three geographic areas"
   AJHG,s67, #1717

7. W Li, A Sherriff, X Liu
   "Assessing risk factors of human complex diseases by Akaike and Bayesian information criteria (AIC and BIC)",
   AJHG,s67, #1203.

8. J Majewski, J Ott
   "Association between GT microsatellite repeats and recombination in the human genome"
   AJHG,s67, #1482.

9. D Nyholt
   "A genome-wide stepwise linear discriminant analysis approach to the genetic analysis of IDDM"
   AJHG,s67, #1822.

10. D Shmulewitz, SC Heath, T Lehner, SB Auerbach, E Asilmaz, ML Blundell, L Petukhova, JD Winick, PC Verlander, Z Han, JL Breslow, J Ott , M Stoffel, JM Friedman
    "Gene mapping and admixture on the island of Kosrae",
    AJHG,s67, #1288.

1999 (49th) Annual Meeting of American Society of Human Genetics (October 19- 23, 1999, San Francisco, CA)

1. AM Alkhateeb, J Al-Alami, SM Leal, HE El-Shanti
   "DNA based testing for the identification of progressive pseudorheumatoid dysplasia carriers",
   AJHG, s65, #1160.
   [ abstract]

2. C Chen, D Gordon, S Finch, N Mendell
   "Comparison of Genehunter 1.2 max LOD, max Heterogeneity LOD, and max NPL statistics for disease gene localization using simulated data",
   AJHG, s65, #1092.
   [ abstract]

3. D Gordon, J Ott
   "Analytic Solution of Detection Rates when Genotype Errors Introduced into Family at Single Nucleotide Polymorphism Locus",
   AJHG, s65, #1396.
   [ abstract]

4. HHH Goring, JD Terwilliger, J Ott
   "A common framework for model-based or model-free, twopoint or multipoint, linkage and/or linkage disequilibrium analysis of complex traits",
   AJHG, s65, #1397.
   [abstract]

5. LR Griffiths1, DR Nyholt, RA Lea, RP Curtain, PJ Brimage
   "Haplotype Analysis of X Linked Migraine Pedigrees Refines the Migraine Susceptibility Locus to Xq24",
   AJHG, s65, #1400.
   [abstract]

6. V Guerrini, S Rutherford, DR Nyholt, LR Griffiths
   "Association of a Glucocorticoid Receptor Gene Marker With Human Essential Hypertension",
   AJHG, s65, #1316
   [abstract]

7. SC Heath, J Ott
   "TDT with errors: a likelihood based approach",
   AJHG, s65, #1412.
   [ abstract]

8. SE Hodge, J Hoh
   "A measure of ambiguity in SNPs in presence of linkage disequilibrium",
   AJHG, s65, #1131
   [ abstract]

9. FM Häfner, T Linder, AA Salam, D Balmer, A Baumer, A Schinzel, T Spillmann, SM Leal ,
   "A novel locus DFNA24 for congenital autosomal dominant hearing loss maps to 4q in a large Swiss German kindred",
   AJHG, s65, #1405
   [ abstract]

10. J Hoh, D Gordon, T Lints, TC Matise, J Ott
    "Computational methods for evaluating clone sampling efficiency in normalized cDNA libraries",
    AJHG, s65, #1255.
    [ abstract]

11. H Knoblauch, B Mueller-Myhsok, A Busjahn, L Ben Avi, S Baehring, H Baron, S Heath, HD Faulhaber, S Shpitzen, A Aydin, A Reshef, R Uhlmann, M Rosenthal, O Eliav, D Schurr, A Lowe5, Y Friedlander, H Schuster, FC Luft, E Leitersdorf
    "A lipid-lowering gene exists on chromosome 13q",
    AJHG, s65, #75
    [ abstract]

12. RA Lea, DR Nyholt, RP Curtain, KL Jordan, LR Griffiths
    "Linkage Analysis of Calcium Channel Genes in Typical Migraine Families"
    AJHG, s65, #1444
    [ abstract]

13. SM Leal, J Ott ,
    "Effects of Stratification in the Analysis of Affected Sib-Pair Data: Benefits and Costs",
    AJHG, s65, #446 (1999).
    [ abstract]

14. O Le Saux, Z Urban, HHH Göring, K Csiszar, FM Pope, A Richard, I Pasquali-Ronquetti, L Bercovitch, MG Lebwohl, M Breuning, P van der Berg, L Kornet, N Doggett, , PTVM Paulus, AAB Bergen, CD Boyd
    "Pseudoxanthoma elasticum maps to an 820 kb region of the p13.1 region of chromosome 16",
    AJHG, s65, #2697
    [ abstract]

15. W Li, F Haghighi
    "Perl as a Tool for Linkage Analysis",
    AJHG, s65, #1452
    [ abstract]

16. TC Matise, JA Gitlin
    "MAP-O-MAT: marker-based linkage mapping on the World Wide Web",
    AJHG, s65, #2464
    [ abstract]

17. DR Nyholt, I Simonic, GS Gericke, D Gordon, J Ott, JL Weber
    "Gilles de la Tourette syndrome: a replication study using family-based analyses of loci associated in an Afrikaner Population",
    AJHG, s65, #2482.
    [abstract]

18. AA Salam, FM Häfner, T Linder, A Baumer, D Balmer, T Spillmann, A Schinzel, SM Leal
    "A novel locus DFNA23 for prelingual autosomal dominant hearing loss maps to 14q in a Swiss German kindred",
    AJHG, s65, #2515
    [abstract]

19. D Shmulewitz, SC Heath, SB Auerbach, ML Blundell, JD Winick, S Signorini, JL Breslow, J Ott, T Lehner, M Stoffel, JM Friedman
    "Genetic epidemiology of Syndrome X disorders on Kosrae",
    AJHG, s65, #455.
    [ abstract]

20. G Snow, E Wijsman, E Thompson, S Heath
    "Multipoint linkage analysis of complex traits with Markov chain Monte Carlo linkage analysis",
    AJHG, s65, #2532
    [ abstract]

21. MK Tayeh, J Al-Alami, MY Al-Sheyyab, SM Leal, HE El-Shanti
    "Linkage Analysis Of A Family With Autosomal Recessive Vitamin B12 Deficiency",
    AJHG, s65, #2411.
    [ abstract]

1998 (48th) Annual Meeting of American Society of Human Genetics (October 27- 31, 1998, Denver, CO)

1. L. Ala-Kokko, S. Annunen, P. Paassilta, J. Lohiniva, M. Perala, T. Pihlajamaa, J. Karppinen, O. Tervonen, H. Kroger, S. Lahde, H. Vanharanta, L. Ryhanen, H. H. Goring, D. J. Prockop
   LINKAGE AND LINKAGE DISEQUILIBRIUM BETWEEN A PUTATIVE MUTATION IN A RARE ALLELE OF THE COL9A2 GENE AND INTERVERTEBRAL DISC DISEASE,
   AJHG, s63, #161 (1998)

2. A. A. Bhat, S. C. Heath, J. Ott,
   HETEROGENEITY FOR MULTIPLE DISEASE LOCI,
   AJHG, s63, #1624 (1998)

3. E. Gillanders, B. Appukuttan, D. Freas-Lutz, S.-H. Juo, S. Villabon, M. Chung, M. Borchert, A. Van Auken, J. Bailey-Wilson, J. Trent, M. Brownstein, T. Stout,
   A SUSCEPTIBILITY LOCUS FOR DUANES RETRACTION SYNDROME (DRS) SUGGESTED BY A GENOME-WIDE SEARCH,
   AJHG, s63, #1679 (1998)

4. D. Gordon, S. Heath, J. Ott ,
   TRUE PEDIGREE ERRORS MORE FREQUENT THAN APPARENT ERRORS FOR SINGLE NUCLEOTIDE POLYMORPHISMS,
   AJHG, s63, #1683 (1998)

5. S. C. Heath,
   A BIAS IN TDT DUE TO UNDETECTED GENOTYPING ERRORS,
   AJHG, s63, #1689 (1998)

6. W. Li ,
   AN EXACT CALCULATION OF THE PROBABILITY OF IDENTITY-BY-DESCENT IN TWO-LOCUS MODELS USING AN EXTENTION OF THE LI-SACKS' METHOD
   AJHG, s63, #1719 (1998)

7. I. Simonic, S. M. Leal, D. Gordon, J. Ott,
   BACKGROUND LINKAGE DISEQUILIBRIUM IN THE AFRIKANER POPULATION OF SOUTH AFRICA ,
   AJHG, s63, #1267 (1998).

8. M. A. Wessman, M. Kallela, I. Hovatta, P. Marttila, M. Kaunisto, M. Koskenvuo, M.-L. Honkasalo, M. Farkkila, J. Ott, J. Kaprio, L. Peltonen, A. Palotie,
   A GENOME-WIDE SEARCH FOR GENES PREDISPOSING TO MIGRAINE IN FINNISH TWINS,
   AJHG, s63, #1817 (1998)

Genetic Analysis Workshop 11, Arcachon, France (September 8-10, 1998)

1. A Bhat, P Lucek, J Ott , Analysis of a complex disease using artificial neural networks

2. CH Chen, SJ Finch, NR Mendell, D Gordon, Comparison of empirical strategies to maximize GENEHUNTER results on linkage data from GAW11 alcoholism pedigree

3. D Gordon, TC Matise, S Heath, J Ott , Effects of random genotype errors on power of multi-allelic transmission disequilibrium test: a study using GAW11 simulated data

4. SH Juo , EW Pugh, A Baffoe-Bonnie, A Kingman, SJM Sorant, AP Klein, J O'Neill, RA Mathias, AF Wilson, JE Bailey-Wilson, Possible linkage of alcoholism, monoamine oxidase (MAO) activity and P300 amplitude to markers on chromosome 12q24

5. S Leal, SC Heath, Markov chain Monte Carlo methods detect alcoholism susceptibility loci on chromosomes 11 and 4

6. W Li , F Haghighi, CT Falk, Design of artificial neural network and its applications to the alcoholism data

7. M Marinovc, TC Matise , GM Lathrop, DE Weeks, A comparison of two algorithms, MultiMap and GMS, for automated construction of genetic linkage maps

1997 (47th) Annual Meeting of American Society of Human Genetics (October 28- November 1, 1997, Baltimore, CA)

1. P. Banerjee, J. A. Knowles, P. Kleyn, B. Ross, G. Penchaszadeh, C. A. Lewis, S. G. Jacobson, J. Ott and T. C. Gilliam, Evaluation of a candidate gene (ther) for the autosomal recessive retinitis pigmentosa 6P21 locus (RP14) , AJHG, s61, #149 (1997).

2. E.W. Daw, S.C. Heath, E.M. Wijsman, Multipoint oligogenic analysis for age of onset data with applications to large Alzheimer disease pedigrees , AJHG, s61, #1588 (1997).

3. S.C. Heath, E.A. Thompson, MCMC samplers for multilocus analyses on complex pedigrees , AJHG, s61, #1623 (1997).

4. S. Du, T.C. Matise, J. Ott , Age-dependency of recombination fraction, AJHG, s61, #1592 (1997).

5. H.H.H. Goring, J.D. Terwilliger, J. Ott , A likelihood-based approach to extended haplotype analysis of shared segments using a Markovian branching process, AJHG, s61, #1614 (1997).

6. W. Li , A complete listing and classification of two-locus two-allele fully-penetrant disease models , AJHG, s61, #1181 (1997).

7. P.R. Lucek, J. Ott , Complex trait analysis using neural networks , AJHG, s61, #1649 (1997).

8. T.C. Matise, C.Kashuk, T. Thangarajah, A. Chakravarti, M. James, Combining radiation hybrid panels to increase mapping power , AJHG, s61, #1386 (1997).

9. B. K. Suarez, C. L. Hampe, C. Zambuto, T. C. Matise , Microsatellite motif and allele frequency divergence, AJHG, s61, #230 (1997)

10. T. Thangarajah, P. J. R. Day, M. Suchard, C. W. Richard III, T. C. Matise , M. R. James, Towards an integrated radiation hybrid map of human chromosome 11 with 100 kb resolution , AJHG, s61, #1425 (1997).

11. H.C. Tsou, D. Teng, X.L. Ping, V. Broncolini, T. Davis, R. Hu, X.X. Xie, A.C. Gruener, A.C. Schrager, A.C. Christiano, C. Eng, P. Steck, J. Ott, S. Tavitigian, M. Peacocke, Role of MMAC1 mutations in early onset breast cancer: causative in association with cowden's syndrome and excluded in BRCA1-negative cases ASHG, s61, #468 (1997).

12. P. S. White, E. P. Sulman, G. M. Brodeur, M. R. James, T. C. Matise , A method for constructing second-generation comprehensive maps of the human genome , AJHG, s61, #1432 (1997).

13. B. Wirth, T. Schmidt, E. Hahnen, S. Rudnik-Schoneborn, M. Krawczak, B. Muller-Myhsok, J. Schonling, K. Zerres. De novo rearrangements found in 2% index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate and implications for genetic counseling , AJHG, s61, #2057 (1997).

1997 (29th) Annual Meeting of the European Society of Human Genetics (?, 1997, Genoa, ITALY)

1. SM Leal, J Winik, S Signorini, M Blundell, S Auerbach, M Stoffel, J Friedman , The genetics of obesity in an isolated Micronesian population.

1996 (46th) Annual Meeting of American Society of Human Genetics (October 29- November 2, 1996, San Francisco, CA)

1. P. Banerjee, J.A. Knowles, Y. Shugart , G. Penchaszadeh, C.A. Lewis, S.G. Jacobson, J.Ott , T.C. Gilliam, Construction of a YAC/BAC contig across the autosomal recessive Retinitis Pigmentosa 6p21 locus and genetic refinement of the disease gene region, AJHG, s59, #1212 (1996).

2. L.M. Brzustowicz, J.P. Gardner, L. Hopp, J. Ott , E. Jeanclos, X.Y. Yang, Z. Fekete, A. Aviv, Genetic linkage studies using cellular phenotypes in transformed lymphoblasts: mapping of a locus for platelet activating factor-evoked calcium response to chromosome 16, and its possible implication for essential hypertension, AJHG, s59, #227 (1996)

3. P. Careera, L. Vismara, M.T. Ghilarducci, V. Brancolini, L. Grimaldi, A. Poluzzi, A. Uncini, Marchioni, A. Giorgetti, M. Ferrari, Mapping of the locus for Familial Hemiplegic Migraine (FHM) within a 1.2 cM interval on 19p, AJHG, s59, #1231 (1996)

4. O.Levran, C. Fann, T. Erlich, J. Ott , A.D. Auerbach, Linkage analysis in Fanconi anemia: refinement of the FAA locus at 16q24.3, AJHG, s59, #1294 (1996)

5. W. Li, V.F.G. Haghighi, T.C. Matise, J. Ott , Using web browser as a graphical user interface for linkage analysis , AJHG, s59, #1782 (1996)

6. T.C. Matise, C. Kashuk, C.W. Richard, A. Chakravarti, M.R. James, Radiation hybrids: panels, distances, densities, and MultiMap, AJHG, s59, #1789 (1996)

7. P.S. White, S.J. Jensen, E.P. Sulman, J.M. Maris, T.C. Matise, P.J. Vojta, J.C. Barrett, G.M. Brodeur, A transcript map of 1p35-36, AJHG, s59, #1831 (1996)

8. C.J. Williams, L.J. Hardwick, S. Butcher, E. Considine, A. Nicod, S. Walsh, D.J. Prockop. F. Caeiro, A. Reginato, V. Brancolini, M. Devoto , A. Carr, M. Lathrop, B.F. Wordsworth, Linkage of chondrocalcinosis to chromosome 5p15.1-.2 in a large Argentinian pedigree , AJHG, s59, #1395 (1996).

Genetic Analysis Workshop 10, Pajaro Dunes Conference Center, Watsonville, CA (October 26-29, 1996)

1. CSJ Fann, FV Haghighi, W Li , Linkage analysis of bipolar disorder using affected sib-pair methods

2. SM Leal, J Ott, Analysis of two-locus traits under heterogeneity for recessive versus dominant inheritance

3. PR Lucek, J Ott , Using neural network algorithms to analyze complex traits in sib pair data

1996 (28th) Annual Meeting of the European Society of Human Genetics (April 11-13, 1996, London, ENGLAND)

1. A. Bolino, V. Brancolini, A. Quattrone, A. Gambardella, G. Romeo, M. Devoto, Homozygosity mapping of a new form of HMSN: autosomal recessive Hypermyelinating Neuropathy , EJHG, 4,s1, p.92 (1996)

2. G. Casari, A. Auricchio, V. Brancolini, P.J. Milla, V.V. Smith, M. Devoto, A. Ballabio, The locus for a novel form of neuronal intestinal pseudoobstruction maps to Xq28 , EJHG, 4,s1, p.1 (1996)

3. Y.Y. Shugart, J. Ott , An empirical approach to distinguish true and false positive lodscore peaks EJHG, 4, s1, 14 (1996)

1995 Annual Meeting of American Society of Human Genetics (October 24-28, 1995, Minneapolis, MN)

1. SE. Antonarakis, JL. Blouin, AE. Pulver, P. Wolyniec, VK. Lasseter, G. Nestadt, R. Babb, HH. Kazazian, B. Dombroski, M. Kimberland, J. Ott , M. Karayiorgou, D. Housman, C. MacLean, A potential susceptibility locus for schizophrenia on chromosome 6p24-6p22 , AJHG, s57, A185 (1995).

2. P. Banerjee, JA. Knowles, Y. Shugart , G. Penchaszadeh, CA. Lewis, SG. Jacobson, J. Ott , TC. Gilliam, Construction of a YAC contig encompassing a locus for autosomal recessive Retinitis Pigmentosa on chromosome 6p21.3 , AJHG, s57, A256 (1995).

3. AAB. Bergen, C. Gambacorti, H. Goerl, J. Lester, M. Kennedy, J. Ott , FS. Zollmann, A new, world-wide, interactive communication and information forum in human genetics on the internet , AJHG, s57, A292 (1995).

4. A. Bolino, V. Brancolini , A. Ouattrone, A. Gambardella, G. Romeo, M. Devoto , Homozygosity mapping of a new form of HMSN: autosomal recessive Hypermyelinating Neuropathy , AJHG, s57, A322 (1995).

5. B. Casey, M. Gebbia, M. Devoto , D. Nelson, A. Aylsworth, Females with midline malformations and complete reversal of left-right asymmetry in a family with apparent X-linked heterotaxy , AJHG, s57, A85 (1995).

6. H. Göring, J. Ott , Verification of sib relationship without knowledge of parental genotypes , AJHG, s57, A192 (1995).

7. H. Kobayashi, L. Baumbach, TC. Matise , A. Schiavi, F. Greenberg, EP. Hoffman, A gene for X-linked infantile spinal muscular astrophy (a severe lethal form of X-linked arthrogryposis) maps to Xp11.3-q11.2 , AJHG, s57, A324 (1995).

8. S. Leal, J. Ott , Analysis of two-locus traits under heterogeneity for dominant versus recessive inheritance , AJHG, s57, A196 (1995).

9. W. Li, CSJ. Fann, J. Ott , Positional difference of male-female genetic distances in all autosomal chromosomes using the computer program TREND , AJHG, s57, A197 (1995).

10. P. Lucek, J. Ott , Neural network algorithms: application in the analysis of complex traits , AJHG, s57, A197 (1995).

11. T. Matise, A. Chakravarti, Automated construction of radiation hybrid maps using MultiMap ,AJHG, s57, A15 (1995).

12. RA. Norman, WK. Chung, L. Power-Kehoe, SC. Chua, Jr., RL. Leigl, M. Devoto, C. Fann, J. Ott , C. Bogardus, E. Ravussin, Genetic linkage studies of homologues to rodent obesity genes in Pima Indians , AJHG, s57, A199 (1995).

1994 Annual Meeting of American Society of Human Genetics (October 18-22, 1994, Montreal, Quebec, CANADA)

1. J. Greenberg, R. Goliath, YY. Shugart , C. Freund, S. Bardien, P. Beighton, R. Ramesar, Localization of a new autosomal dominant Retinitis Pigmentosa gene on chromosome 17p and screening of candidate genes , AJHG, s55, A186 (1994).

2. VK. Lasseter, AE. Pulver, P. Wolyniec, L. Kasch, G. Nestadt, ZZ. Kazazian, D. Housman, M. Karayiorgou, SE. Antonarakis, D. Meyers, R. Babb, M. Kimberland, KY. Liang, J. Ott, JL. Blouin, HM. Chen, M. Lalioti, M. Morris, Schizophrenia: A genome search targets chromosomes 3 and 8 for exploration , AJHG, s55, A192 (1994).

3. A. Lazzarini, ES. Stenroos, T. Lehner, V. McKoy, B. Gold, MK. McCor-mack, CS. Reid, J. Ott, WG. Johnson, STRP linkage studies in a new family with X-linked mental retardation: Tight linkage to DXS458 , AJHG, s55, A192 (1994).

4. P. Lucek, J. Ott GLM: A relational database system for linkage mapping on PC compatibles , AJHG, s55, A156 (1994).

5. P. Pekkarinen, PE. Bredbacka, J. Terwilliger , I. Hovatta, J. Lonnqvist, L. Peltonen, Evidence for a susceptibility locus for manic-depressive disorder in Xq26 , AJHG, s55, A27 (1994).

6. YY. Shugart , JA Knowles, P. Banerjee, TC. Gilliam, CA. Lewis, SG. Jacobson, J. Ott Linkage analysis of a new locus for autosomal recessive retinitis pigmentosa (arRP) on chromosome 6p , AJHG, s55, A15(1994).

7. ES. Stenroos, WG. Johnson, A. Lazzarini, SH. Subramony, T. Lehner, VV. McKoy, A. Brice, J. Ott, RD. Currier, Linkage studies in three North American SCA pedigrees , AJHG, s55, A204 (1994).

8. JD. Terwilliger, J. Ott A powerful one degree of freedom approach to mapping genes with linkage disequilibrium , AJHG, s55,A166 (1994).

9. AL. Zhang, M. Devoto , G. Tomeo, DT. Case, Exclusion of the RET proto-oncogene as candidate for total colonic aganlionosis in the Spotting Lethal (sl) rat strain , AJHG, s55, A124 (1994).

1993 Annual Meeting of American Society of Human Genetics (October 5-9, 1993, New Orlean, LA)

1. B. Casey, M. Devoto , KL. Jones, A. Ballabio, X-linked visceral heterotaxy maps to Xq25-q26 , AJHG, s53, #137 (1993).

2. M. Devoto , A. Bolino, G. Enia, C. Zoccali, G. Romeo, A new form of X-linked hypophosphatemic rickets with hypercalciuria (HPDR II) maps in the Xp11 region , AJHG, s53, #993 (1993).

3. CSJ. Fann, J. Ott , Partitioning the differences between male and female map distances in human gene mapping , AJHG, s53, #998 (1993).

4. JA. Knowles, VJ. Vieland, AJ. Fyer, G. Heiman, H. Rassnick, LD. Fine, TL. Austin, P. Adams, SE. Hodge, DF. Klein, J. Ott, MM. Weissman, TC. Gilliam Genetic linkage analysis of panic disorder , AJHG, s53, #1023 (1993).

5. T. Lehner, RE. Straub, E. Loth, JR. Alexander, Y. Luo, W. Shao, L. Sharpe, R. Simons, M. Gibbon, B. Lerer, J. Endicott, TC. Gilliam, J. Ott, M. Baron Power and sensitivity analysis of a large family with bipolar affective disorder, potentially linked to the marker PFKL (21q22.3) , AJHG, s53, #1030 (1993).

6. C. Merette , M. Martinez, V. Raymond, M. Maziade, The 11q21-22 region in preliminary linkage studies of schizophrenia (SZ) and bipolar pedigrees (BP) of Eastern Quebec: methodological implications, AJHG, s53, #1042 (1993).

7. C. Merette, LM. Brzustowicz, RJ. Daniels, KE. Davies, TC. Gilliam, J. Melki, MA. Pericak-Vance, T. Siddique, B. Wirth, J. Ott , An investigation of genetic heterogeneity and linkage disequilibrium with 161 spinal muscular atrophy families , AJHG, s53, #1045 (1993).

8. K. Petrukhin, R.E. Tanzi, S.G. Fischer, M. Pirastu, I. Chernov, B. Boukhgalter, E. Cyanis, W. Wasco, L.M. Brzustowicz, D. Matseoane, M. Devoto, A.L. Figlis, J. Lolidihnos, A. Cao, I. Chumakov, G. Evgrafov, I. Sternlieb, D. Warburton, G. Penchaszadeh, I.H. Scheinberg, T.C. Gilliam, Mapping the Wilson's disease gene , AJHG, s53, #55 (1993).

9. M. Pirastu, P. Cossu, A. Loi, AL. Nucaro, M. Deiana, J. Loudianos, A. Angius, V. Dessi, S. DeVirgilis, A. Cao, A.L. Figus, G. Farci, A. Balestrieri, AM. Nurchi, A. Deplano, M. Devoto, L.M. Brzustowicz, V. K. Petrukhin, I.P. Chernov, T.C. Gilliam, A founder effect for Wilson's disease in Sardinia defined by linkage disequilibrium mapping , AJHG, s53, #844 (1993).

10. AE. Pulver, M. Karayiorgou, P. Wolyniec, S. Antonarakis, D. Housman, L. Kasch, H. Hazazian, M. Lamacz, VK. Lasseter, J. McGrath, D. Meyers, J. Nestadt, J. Ott, E. Ramu, M. Kimberland, R. Babb, N. DeMarchi, B. Childs, A potential linkage for schizophrenia on chromosome 22q12-q13 , AJHG, s53, #1063 (1993).

11. G. Romeo, L. Yin, I. Ceccherini, B. Pasini, I. Matera, V. Barone, T. Tocco, H. Kaariainen, D. Weber, M. Devoto , Autosomal dominant Hirschsprung disease: close linkage with the ret proto-oncogene and deletion mapping of the region , AJHG, s53, #133 (1993).

12. YY. Shugart, CSJ. Fann, J. Ott , Modeling a "natural" mapping function , AJHG, s53, #1076 (1993).

13. LD. Spotila, J. Caminis, M. Devoto, L. Sereda, MP. Whyte, J. Ott, AM.Tenenhouse, DJ. Prockop, Bimodal distribution of bone mineral density in five families with osteoporosis suggests a simple mode of inheritance , AJHG, s53, #1715 (1993).

14. RE Straub, T. Lehner, JE Loth, JR Alexander, Y Luo, W Shao, L Sharpe, R Simon, M Gibbon, B Lerer, J Endicott, J. Ott, M. Baron, TC. Gilliam, PFKL and other microsatellite markers in 21q22.3 yield positive lod scores in one of 42 bipolar affective disorder families tested , AJHG, s53, #265 (1993).

15. PJ. Tienari, JD. Terwilliger, J. Palo, J. Ott, L. Peltonen, Two-locus linkage analysis in multiple sclerosis AJHG, s53, #267 (1993).

16. X. Xie, J. Ott , Testing linkage disequilibrium between a disease gene and marker loci, AJHG, s53,Am J Hum Genet 53, 1107 (abstract)

1993 World Congress on Psychiatric Genetics (October 2-5, 1993, New Oeleans, LA)

1. Baron M, Endicott J, Lerer B, Loth JE, Alexander JR, T. Lehner, J. Ott A pedigree series for mapping disease genes in bipolar affective disorder: sampling and assessment procedures , Psychiatric Genetics, 3, 143 (1993).

2. Crow TJ, Delisi LE, Lofthouse R, Poulter M, T. Lehner, Bass N, Shah T, Walsh C, Boccio-Smith A, Shields G, J. Ott An examination of linkage of schizophrenia and schizo-affective disorder to the pseudo-autosomal region , Psychiatric Genetics 3, 125 (1993).

3. M. Devoto, Poulter M, Lofthouse R, Bass N, Boccio A, Shields G, J. Ott, T. Lehner , Crow TJ, Delisi LE, Genetic linkage analysis of schizophrenia and X chromosome polymorphic markers using X-specific and XY-homologous gene models , Psychiatric Genetics 3, 126 (1993).

4. Knowles JA, Vieland VJ, Fyer A, Heiman G, Rassnick H, Fine L, Austin TL, Adams P, Hodge SE, Klein DF, J. Ott, Weissman MM, Gilliam TC, Genetic linkage analysis of panic disorder , Psychiatric Genetics 3, 128 (1993).

5. Pulver AE, Karayiorgou M, Demarchi N, Antonarakis S, Housman D, Kasch L, Kazazian H, Lamacz M, Lasseter VK, McGrath J, Meyers D, Nestadt G, J. Ott, Ramu E, Wolyniec P, Childs B, A potential linkage for schizophrenia on chromosome 22q12-q13 , Psychiatric Genetics 3, 126 (1993).

6. Pulver AE, Karayiorgou M, Demarchi N, Antonarakis S, Housman D, Kasch L, Kazazian H, Lamacz M, Lasseter VK, McGrath J, Meyers D, Nestadt G, J. Ott, Ramu E, Wolyniec P, Childs B, Searching the genome for markers associated with schizophrenia: a progress report on a two-stage strategy , Psychiatric Genetics 3, 151 (1993).

7. Straub RE, Lehner T, Loth JE, Alexander JR, Shao W, Luo Y, Sharpe L, Simon R, Gibbon M, Lerer B, Endicott J, J. Ott, Gilliam TC, Baron M , Linkage analysis of bipolar affective disorder: summary of genomic screening results and positive lod scores with markers in region 21q22.3 in one large family , Psychiatric Genetics 3, 124 (1993).

8. JD. Terwilliger, J. Ott , On the interpretation of two-trait locus/two-marker locus lod scores , Psychiatric Genetics 3, 136 (1993).

9. Tienari PJ, JD. Terwilliger, J. Ott, Palo J, Peltonen L , Analysis of two susceptibility genes in multiple sclerosis. Two locus linkage in multiplex families , Psychiatric Genetics 3, 127 (1993).

1992 Annual Meeting of American Society of Human Genetics (November 9-13, 1992, San Francisco, CA)

1. Brzustowicz LM, Townsend L, Asokan S, Gilliam TC, Ott J , Prevalence and effects of errors in genotype databases , AJHG, s51, A49 (1992).

2. Gal A, Bunge S, Wedemann H, Aulehla-Scholz C, David D, Terwilliger JD, Horn M, Denton M, Schwinger E, Schinzel A, Ott J, Bleeker-Wagemakers EM, Molecular analysis and mapping of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa AJHG, s51, A6 (1992).

3. Kleyn PW, Brzustowicz LB, Soares V, Knowles J, Vitale E, C. Merette , Penchaszadeh G, Palmer D, Wang C, Jie P, Grunn A, Lien L, Yu M-T, Warburton D, Kunkel LM, Munsat T, Ott J, Gilliam TC, Physical and genetic mapping of the Spinal Muscular Atrophy locus , AJHG, s51, A192 (1992).

4. Knowles JA, Vieland VJ, Fyer A, Stefanovich M, Freimer NF, Woodley K, White P, Heiman G, Rassnick H, Lish J, Adams P, Klein DF, Ott J, Weissman MM, Gilliam TC, Genetic linkage analysis of panic disorder , AJHG, s51, A365 (1992).

5. Leal SM, Ott J , The RISK computer program to calculate risk support intervals , AJHG, s51, A101 (1992).

6. C. Merette, L.M. Brzustowicz, Gilliam TC, Daniels RJ, Davies KE, Melki J, Siddique T, Pericak-Vance MA, Wirth B, Ott J , An international linkage analysis of chronic childhood-onset spinal muscular atrophy , AJHG, s51, A368 (1992).

7. Ott J, Terwilliger JD, Xie X , Determining the informativeness of untyped individuals in a pedigree analysis , AJHG, s51, A197 (1992).

8. Petrukhin KE, Speer MC, Bonaldo MF, Fischer S, Warburton D, Ott J, Gilliam TC, Isolation, characterization, and genetic mapping of human chromosome 13 microsatellites markers , AJHG, s51, A198 (1992).

9. Pulver A, Karayiorgou M, DeMarchi N, Antonarakis S, Housman D, Kasch L, Kazazian H, Lamacz M, Lasseter K, Kimberland M, Meyers D, Nestadt G, Ott J, Wolyniec P, Childs B, Exclusion of linkage between schizophrenia and significant regions of the human genome , AJHG, s51, A371 (1992).

10. Shugart YY, Ott J , Significance tests relating to heterozygosity , AJHG, s51, A159 (1992).

11. Speer M, Terwilliger JD, Ott J , A chromosome-based method for rapid computer simulation , AJHG, s51, A202 (1992).

12. Straub RE, Baron M, Lehner T, Loth JE, Luo Y, Shao W, Wexler SN, Sharpe L, Simon R, Gibbon M, Endicott J, Ott J, Gilliam TC, Bipolar affective illness: results of linkage analysis using microsatellite markers , AJHG, s51, A374 (1992).

13. Terwilliger JD, Ott J , A novel approach to combining data from multiple linked loci into a maximally heterozygous "super-locus" yields greatly increased power in 2-point linkage and sib-pair analysis , AJHG, s51, A202 (1992).

14. Xie X, Ott J , Finding all loops in a pedigree , AJHG, s51, A206 (1992).

1991 Annual Meeting of American Society of Human Genetics (October 6-11, 1991, Washington DC)

1. L.M. Brzustowicz, T. Lehner, PW Kleyn, TL Munsat, J. Ott, TC Gilliam , Evaluation of non-allelic genetic heterogeneity among the childhood-onset spinal muscular atrophies , AJHG, s49, 337 (1991).

2. Y. Ding, JD Terwilliger, J. Ott , On the effects of heterozygosity and intermarker distance on mapping a new locus against a complete map , AJHG, s49,367 (1991).

3. T. Helio, A. Palotie, K. Totterman. J. Ott. R. Kauppinen-Makelin, M. Tikkanen, Lack of association between the apoprotein B gene 3' hypervariable region alleles and coronary artery disease in Finnish patients with angiographically documented coronary artery disease , AJHG, s49, 140 (1991).

4. PW Kleyn, LM Brzustowicz, T. Lehner, LL Lien, FM Boyce, JM Miller, M. McPherson, T. Thompson, JJ Wasmuth, TL Munsat, LM Kunkel, J. Ott, TC Gilliam, Mapping the disease locus for the spinal muscular atrophies , AJHG, s49, 346 (1991).

5. J. Knowles, A. Fyer, M. Stefanovich, NF Freimer, V. Vieland, J. Lish, P. Adams, DF Klein, TC Gilliam, MM Weissman, J. Ott , Genetic linkage analysis of panic disorder , AJHG, s49, 347 (1991).

6. C. Merette, J. Ott , HOMAGE: a computer program to perform a homogeneity test using age at onset as a covariate , AJHG, s49, 351 (1991).

7. RE Straub, M. Baron, T. Lehner, D. Weeks, Y. Luo, SN Wexler, J. Ott, TC Gilliam , Genetic linkage analysis of bipolar affective disorder , AJHG, s49, 361 (suppl)

8. JD Terwilliger, T. Lehner, J. Ott , Differential sex dependent penetrances of autosomal dominant diseases mimic linkage to the boundary of the pseudoautosomal region , AJHG, s49, 367 (1991).

9. DE Weeks, J. Ott, GM Lathrop, Multipoint mapping under different models of genetic interference using the LINKAGE programs , AJHG, s49, 372 (1991).

1990 Annual Meeting of American Society of Human Genetics (October 16-20, 1990, Cincinnati, OH)

1. GM Lathrop, J. Ott , Analysis of complex diseases under oligogenic models and intrafamilial heterogeneity by the LINKAGE programs , AJHG, s47, A188 (1990).

2. SM Leal, J. Ott , Expected lod scores in linkage analysis of autosomal recessive traits for affected and unaffected offspring , AJHG, s47, A188 (1990).

3. JD Terwilliger, DE Weeks, J. Ott , Laboratory errors in the reading of marker alleles cause massive reductions in lod score and lead to gross overestimates of the recombination fraction , AJHG, s47, A201 (1990).

4. DE Weeks, J. Ott, GM Lathrop, SLINK: a general simulation program for linkage analysis , AJHG, s47, A204 (1990).

5. X. Xie, J. Ott , Determining the effect of a change in affection status on the lod score , AJHG, s47, A205 (1990).

1989 Annual Meeting of American Society of Human Genetics (November 11-15, 1989, Baltimore, Maryland)

1. J. Ott , Effects on gene mapping of unequal marker heterozygosity , AJHG, s45, A156 (1989).

1988 Annual Meeting of American Society of Human Genetics (October 12-15, 1988, New Orlean, LA)

1. Hejtmancik JF, J. Ott, Chakraborty R, Ichiye K, Caskey CT, Daiger SP, Duchenne muscular dystrophy locus at Xp21: multipoint linkage analysis, linkage disequilibrium studies and heterogeneity mapping , AJHG, s43, A146 (1988).

2. J. Ott, T. Lehner, LA Sandkuyl , Fallacies of the technique of "haplotyping" two apparently linked loci in multipoint linkage analysis , AJHG, s43, A154 (1988).

3. LA Sandkuyl, J. Ott , Predicting genetic risks by computer simulation , AJHG, s43, A171 (1988).

4. Shiloh Y, L. Sandkuyl, Litvak G, Ziv Y, Hildesheimer M, Buchris V, J. Ott , Localization of X-linked albinism-deaf- ness syndrome (ADFN) to the region Xq26.3-27.1 by linkage analy- sis , AJHG, s43, A158 (1988).

5. Zoghbi HY, LA Sandkuyl, J. Ott, Daiger SP, O'Brien WE, Beaudet AL, Multilocus linkage analysis localizes the gene for autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6 , AJHG, s43, A164 (1988).

1987 Annual Meeting of American Society of Human Genetics (October 7-10, 1987, San Diego, CA)

1. G. Litvak, L. Sandkuyl, J. Ott, V. Buchris, M. Hildesheimer, Y. Shiloh, Localization of X-linked albinism-deafness syndrome to Xq by linkage with DNA markers , AJHG, s41, A174 (1987).