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Jurg Ott

Research Profile

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Procedures

Chromosome Mapping

Disorders

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Publications

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S Barral; David A Bennett; Thomas D Bird; B F Boeve; Ramon Diaz-Arrastia; M R Farlow; Tatiana Foroud; A Goate; N Graff-Radford; Richard Mayeux; Jurg Ott; Yaakov Stern; R A Sweet; R S Wilson
Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory.
Shuang Wang; Chad Haynes; Francis Barany; Jurg Ott
Genome-wide autozygosity mapping in human populations.
Amalia Martinez-Mir; Abraham Zlotogorski; Derek Gordon; Lynn Petukhova; Jianhong Mo; T Conrad Gilliam; Douglas Londono; Chad Haynes; Jurg Ott; Maria Hordinsky; Krassimira Nanova; David Norris; Vera H Price; Madeleine Duvic; Angela M Christiano
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.

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All Publications

2012: S Barral; David A Bennett; Thomas D Bird; B F Boeve; Ramon Diaz-Arrastia; M R Farlow; Tatiana Foroud; A Goate; N Graff-Radford; Richard Mayeux; Jurg Ott; Yaakov Stern; R A Sweet; R S Wilson
Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory.
Neurology 2012;78(19):1464-71.
2009: Shuang Wang; Chad Haynes; Francis Barany; Jurg Ott
Genome-wide autozygosity mapping in human populations.
Genetic epidemiology 2009;33(2):172-80.
2007: Amalia Martinez-Mir; Abraham Zlotogorski; Derek Gordon; Lynn Petukhova; Jianhong Mo; T Conrad Gilliam; Douglas Londono; Chad Haynes; Jurg Ott; Maria Hordinsky; Krassimira Nanova; David Norris; Vera H Price; Madeleine Duvic; Angela M Christiano
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.
American journal of human genetics 2007;80(2):316-28.
2005: Jinfeng Xu; Yaning Yang; Jurg Ott
Survival analysis of microarray expression data by transformation models.
Computational biology and chemistry 2005;29(2):91-4.
2003: Amalia Martinez-Mir; Abraham Zlotogorski; Jurg Ott; Derek Gordon; Angela M Christiano
Genetic linkage studies in alopecia areata.
The journal of investigative dermatology. Symposium proceedings / the Society for Investigative Dermatology, Inc. [and] European Society for Dermatological Research 2003;8(2):199-203.
2003: Ana Kljuic; Hisham Bazzi; John P Sundberg; Amalia Martinez-Mir; Ryan O'Shaughnessy; My G Mahoney; Moise Levy; Xavier Montagutelli; Wasim Ahmad; Vincent M Aita; Derek Gordon; Jouni Uitto; David Whiting; Jurg Ott; Stuart Fischer; T Conrad Gilliam; Colin A B Jahoda; Rebecca J Morris; Andrey Panteleyev; Vu Thuong Nguyen; Angela M Christiano
Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.
Cell 2003;113(2):249-60.
2003: Jianjun Liu; Suh-Hang Hank Juo; A Dewan; Adina Grunn; Xiaomei Tong; Miguel Brito; Naeun Park; JE Loth; Kyra Sarner Kanyas; Bernard Lerer; Jean Endicott; Graciela Penchaszadeh; James A Knowles; Jurg Ott; T Conrad Gilliam; M Baron
Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.
Molecular psychiatry 2003;8(3):333-42.
2002: Amalia Martinez-Mir; Derek Gordon; Liran Horev; Laurent Klapholz; Jurg Ott; Angela M Christiano; Abraham Zlotogorski
Multiple cutaneous and uterine leiomyomas: refinement of the genetic locus for multiple cutaneous and uterine leiomyomas on chromosome 1q42.3-43.
The Journal of investigative dermatology 2002;118(5):876-80.
2001: Jianjun Liu; D R Nyholt; P Magnussen; Enrico Parano; Piero Pavone; Daniel Geschwind; Catherine Lord; P Iversen; J Hoh; Jurg Ott; T Conrad Gilliam
A genomewide screen for autism susceptibility loci.
American journal of human genetics 2001;69(2):327-40.
1999: Jorge Frank; Claudio Pignata; Andrey Panteleyev; David Prowse; Howard P Baden; Lorin Weiner; L Gaetaniello; Wasim Ahmad; N Pozzi; Peter B Cserhalmi-Friedman; Vincent M Aita; Hendrik Uyttendaele; D Gordon; Jurg Ott; Janice L Brissette; Angela M Christiano
Exposing the human nude phenotype.
Nature 1999;398(6727):473-4.
1998: Wasim Ahmad; V Brancolini; M F ul Faiyaz; HaMut Lam; S ul Haque; M Haider; A Maimon; Vincent M Aita; J Owen; D Brown; D J Zegarelli; M Ahmad; Jurg Ott; Angela M Christiano
A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.
American journal of human genetics 1998;62(4):987-91.
1998: James A Knowles; P A Rao; T Cox-Matise; JE Loth; GM de Jesus; L Levine; Kamna Das; Graciela Penchaszadeh; J R Alexander; Bernard Lerer; Jean Endicott; Jurg Ott; T Conrad Gilliam; M Baron
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 1998;62(4):916-24.
1998: P Banerjee; C A Lewis; P W Kleyn; Yin Yao Shugart; Barbara M Ross; Graciela Penchaszadeh; Jurg Ott; S G Jacobson; T Conrad Gilliam; James A Knowles
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.
Genomics 1998;48(2):171-7.
1998: P Banerjee; P W Kleyn; James A Knowles; C A Lewis; Barbara M Ross; Enrico Parano; S G Kovats; J J Lee; Graciela Penchaszadeh; Jurg Ott; S G Jacobson; T Conrad Gilliam
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.
Nature genetics 1998;18(2):177-9.
1998: Wasim Ahmad; Muhammad Faiyaz-Ul-Haque; V Brancolini; HC Tsou; S ul Haque; HaMut Lam; Vincent M Aita; J Owen; M deBlaquiere; J Frank; Peter B Cserhalmi-Friedman; A Leask; John A McGrath; M Peacocke; M Ahmad; Jurg Ott; Angela M Christiano
Alopecia universalis associated with a mutation in the human hairless gene.
Science (New York, N.Y.) 1998;279(5351):720-4.
1997: HC Tsou; David Teng; XL Ping; V Brancolini; T Davis; R Hu; XX Xie; AC Gruener; CA Schrager; Angela M Christiano; Charis Eng; PA Steck; Jurg Ott; Sean V Tavtigian; M Peacocke
The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases.
American journal of human genetics 1997;61(5):1036-43.
1997: P R Lucek; Jurg Ott
Neural network analysis of complex traits.
Genetic epidemiology 1997;14(6):1101-6.
1996: TC Matise; H Onis-Keller; Jurg Ott
Meeting report. Statistical methods in genetic mapping.
Genomics 1996;36(1):223-5.
1995: Yin Yao Shugart; P Banerjee; James A Knowles; C A Lewis; Samuel G Jacobson; T C Matise; Graciela Penchaszadeh; T Conrad Gilliam; Jurg Ott
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.
American journal of human genetics 1995;57(2):499-502.
1995: Jurg Ott
Linkage analysis with biological markers.
Human heredity 1995;45(3):169-74.
1994: James A Knowles; Yin Yao Shugart; P Banerjee; T Conrad Gilliam; C A Lewis; Samuel G Jacobson; Jurg Ott
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p.
Human molecular genetics 1994;3(8):1401-3.
1994: M Baron; R E Straub; T Lehner; J Endicott; Jurg Ott; T Conrad Gilliam; Bernard Lerer
Bipolar disorder and linkage to Xq28.
Nature genetics 1994;7(4):461-2.
1994: Jurg Ott; H Donis-Keller
Statistical methods in genetic mapping.
Genomics 1994;22(2):496-7.
1994: S M Leal; Jurg Ott
A likelihood approach to calculating risk support intervals.
American journal of human genetics 1994;54(5):913-7.
1993: Linda M Brzustowicz; C Mérette; X Xie; L Townsend; T Conrad Gilliam; Jurg Ott
Molecular and statistical approaches to the detection and correction of errors in genotype databases.
American journal of human genetics 1993;53(5):1137-45.
1993: Linda M Brzustowicz; C Mérette; P W Kleyn; T Lehner; L H Castilla; Graciela Penchaszadeh; Kamna Das; T L Munsat; Jurg Ott; T Conrad Gilliam
Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.
Human heredity 1993;43(6):380-7.
1993: Jurg Ott
Detecting marker inconsistencies in human gene mapping.
Human heredity 1993;43(1):25-30.
1993: Konstantin Petrukhin; M C Speer; Eftihia Cayanis; MF Bonaldo; U Tantravahi; MB Soares; SG Fischer; Dorothy Warburton; T Conrad Gilliam; Jurg Ott
A microsatellite genetic linkage map of human chromosome 13.
Genomics 1993;15(1):76-85.
1993: Joseph D Terwilliger; Jurg Ott
A novel polylocus method for linkage analysis using the lod-score or affected sib-pair method.
Genetic epidemiology 1993;10(6):477-82.
1993: S M Leal; Jurg Ott
A bootstrap approach to estimating power for linkage heterogeneity.
Genetic epidemiology 1993;10(6):465-70.
1993: C Mérette; T Lehner; Jurg Ott
Two new approaches toward linkage heterogeneity of FAD: two-locus models and age of onset as a discriminator.
Genetic epidemiology 1993;10(6):455-9.
1993: Joseph D Terwilliger; M Speer; Jurg Ott
Chromosome-based method for rapid computer simulation in human genetic linkage analysis.
Genetic epidemiology 1993;10(4):217-24.
1993: Michelle M Le Beau; J Overhauser; R E Straub; G Silverman; T Conrad Gilliam; Jurg Ott; P O'Connell; U Francke; A Geurts van Kessel
Report of the first international workshop on human chromosome 18 mapping.
Cytogenetics and cell genetics 1993;63(2):78-96.
1993: R E Straub; M C Speer; Y Luo; K Rojas; J Overhauser; Jurg Ott; T Conrad Gilliam
A microsatellite genetic linkage map of human chromosome 18.
Genomics 1993;15(1):48-56.
1992: Jurg Ott
Strategies for characterizing highly polymorphic markers in human gene mapping.
American journal of human genetics 1992;51(2):283-90.
1992: Linda M Brzustowicz; P W Kleyn; F M Boyce; L L Lien; Anthony P Monaco; Graciela Penchaszadeh; Kamna Das; C H Wang; T L Munsat; Jurg Ott
Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.
Genomics 1992;13(4):991-8.
1992: Joseph D Terwilliger; Y Ding; Jurg Ott
On the relative importance of marker heterozygosity and intermarker distance in gene mapping.
Genomics 1992;13(4):951-6.
1992: C Mérette; Mary-Claire King; Jurg Ott
Heterogeneity analysis of breast cancer families by using age at onset as a covariate.
American journal of human genetics 1992;50(3):515-9.
1992: Veronica J Vieland; David A Greenberg; Susan E Hodge; Jurg Ott
Linkage analysis of two-locus diseases under single-locus and two-locus analysis models.
Cytogenetics and cell genetics 1992;59(2-3):145-6.
1992: Joseph D Terwilliger; Jurg Ott
A multisample bootstrap approach to the estimation of maximized-over-models lod score distributions.
Cytogenetics and cell genetics 1992;59(2-3):142-4.
1992: Joseph D Terwilliger; Jurg Ott
A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.
Human heredity 1992;42(6):337-46.
1990: M Baron; R Hamburger; L A Sandkuyl; N Risch; B Mandel; Jean Endicott; R H Belmaker; Jurg Ott
The impact of phenotypic variation on genetic analysis: application to X-linkage in manic-depressive illness.
Acta psychiatrica Scandinavica 1990;82(3):196-203.
1990: Jurg Ott
Cutting a Gordian knot in the linkage analysis of complex human traits.
American journal of human genetics 1990;46(2):219-21.
1990: Jurg Ott; S Bhattacharya; J D Chen; Michael J Denton; J Donald; Christopher Dubay; G J Farrar; Gerald A Fishman; D Frey; Andreas Gal
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(2):701-4.
1990: Jurg Ott; J Caesar; M Mächler; A Schinzel; W Schmid
Presymptomatic exclusion of myotonic dystrophy in a one-generation pedigree of half-siblings.
Human heredity 1990;40(5):305-7.
1990: Daniel E Weeks; T Lehner; E Squires-Wheeler; C Kaufmann; Jurg Ott
Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis.
Genetic epidemiology 1990;7(4):237-43.
1990: Daniel E Weeks; Linda M Brzustowicz; E Squires-Wheeler; Barbara Cornblatt; T Lehner; M Stefanovich; A Bassett; T Conrad Gilliam; Jurg Ott; L Erlenmeyer-Kimling
Report of a workshop on genetic linkage studies in schizophrenia.
Schizophrenia bulletin 1990;16(4):673-86.
1989: Jurg Ott
Computer-simulation methods in human linkage analysis.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(11):4175-8.
1989: L Sandkuyl; Jurg Ott
Determining informativity of marker typing for genetic counseling in a pedigree.
Human genetics 1989;82(2):159-62.
1989: Jurg Ott
Statistical properties of the haplotype relative risk.
Genetic epidemiology 1989;6(1):127-30.
1989: T Lehner; L A Sandkuyl; Jurg Ott
Linkage analysis for a disease with a complex mode of inheritance in a simulated data set.
Progress in clinical and biological research 1989;329():141-6.