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Human Genome Sequence Variation and the Inherited Basis of Common Disease (J1)

Organizer(s): David M. Altshuler, Lon Cardon and Leonid Kruglyak
January 8 - 13, 2004
Beaver Run Resort  ·  Breckenridge, Colorado
Abstract Deadline: October 15, 2003
Early Registration Deadline: November 10, 2003


Supported by Keystone Symposia

Joint meeting: Natural Variation and Quantitative Genetics in Model Organisms (J2)
NOTE: Registration for meeting allows attendance at joint meeting (pending space availability).



This meeting took place in the 2004 season.

For a complete list of the meetings for the upcoming/current season,
see our meeting list, or search for a meeting.
Summary of Meeting
The goal of this meeting is to understand patterns of sequence variation in the human genome and how they impact biology and disease. Specifically, the meeting will explore how genome sequences and patterns of gene expression vary in populations, and the forces that shaped these patterns (both molecular and demographic). We will review approaches to studying complex traits in both model systems and in human populations, including the genetic architecture of common human diseases. Finally, we will review recent examples of genetic contributions to common human diseases, and the impact of such information on biology, pharmaceutical development and medicine. The goal of the joint meetings is to bring together scientists and perspectives from population genetics, quantitative genetics, human genetics, genomics and epidemiology. The synthesis of these capabilities and frameworks will surely be required to make progress in the genetic analysis of common human disease.

Thursday, January 8
3:00 - 7:00 PM Registration Foyer
6:15 - 7:15 PM Refreshments Foyer
7:15 - 7:30 PM Orientation Peaks 4-5
7:30 - 9:30 PM Keynote Session: Genetic Dissection of Complex Traits (Joint) Peaks 4-5
* David M. Altshuler, Massachusetts General Hospital
* Detlef Weigel, Max Planck Institute for Developmental Biology
Charles H. Langley, University of California, Davis
Polymorphism and Divergence Across the Drosophila Genome
Aravinda Chakravarti, Johns Hopkins School of Medicine
The Nature of Variation in Complex Disease
Friday, January 9
7:00 - 8:00 AM Breakfast Peaks 6-12
8:00 - 11:00 AM Patterns of Human Genome Sequence Variation Peaks 4-5
* Peter Donnelly, University of Oxford
Mark Daly, Massachusetts General Hospital
Human Haplotype Structure
Lon Cardon, University of Oxford
Haplotype Structure Across Chromosomes
Kelly A. Frazer, The Scripps Research Institute
Genetic Variation and Human Disease
Andrew G. Clark, Cornell University
Lessons from Candidate Gene Studies about the Genetics of Complex Traits
9:20 - 9:40 AM Coffee Break Foyer
11:00 AM - 1:00 PM Poster Setup Peaks 14-16
1:00 - 10:00 PM Poster Viewing Peaks 14-16
4:30 - 5:00 PM Coffee & Snacks Available Foyer
5:00 - 7:00 PM Exploiting Inbred Strains to Find Complex Traits (Joint) Peaks 4-5
* Peter D. Keightley, University of Edinburgh
Keith R. Davis, Icoria, Inc
High-Throughput Plant Gene Function Analysis in Arabidopsis
Wayne Frankel, The Jackson Laboratory
Effects of Genetic Background on Induced and Spontaneous Mouse Models for Epilepsy
Michael Snyder, Stanford University School of Medicine
Identification of Functional Regions in the Genomes of Yeast and Humans
6:45 - 7:20 PM Comparative Genomics
Eric S. Lander, Broad Institute, Massachusetts Institute of Technology
7:20 - 8:00 PM Social Hour Peaks 14-16
7:30 - 10:00 PM Poster Session 1 Peaks 14-16
Saturday, January 10
7:00 - 8:00 AM Breakfast Peaks 6-12
8:00 - 11:00 AM Molecular Forces Shaping Genome Sequence Variation Peaks 4-5
* Andrew G. Clark, Cornell University
Peter Donnelly, University of Oxford
Understanding Fine-Scale Variation in Recombination Rates
Richard Hudson, University of Chicago
Fine-Scale Mapping with Linkage Disequilibrium
Chris Toomajian, University of Southern California
The Pattern of Polymorphism in the Arabidopsis Genome
Evan E. Eichler, University of Washington
Structural Variation and Large-Scale Polymorphism within Segmental Duplications
Richard M. Durbin, Wellcome Trust Sanger Institute
Short Talk: Significant Correspondence of Recombination Events in Pedigrees with Haplotype Block Boundaries
9:20 - 9:40 AM Coffee Break Foyer
11:00 AM - 1:00 PM Poster Setup Peaks 14-16
1:00 - 10:00 PM Poster Viewing Peaks 14-16
4:30 - 5:00 PM Coffee & Snacks Available Foyer
5:00 - 7:00 PM Population History and Human Sequence Variation Peaks 4-5
* Stephen J. O'Brien, National Cancer Institute, National Institutes of Health
David B. Goldstein, Duke University
Haployptes, Human History, and Pharmacogenetics
John Raelson, Galileo Genomics
Short Talk: General Extent of LD in the Quebec Founder Population
Mark Patterson, Public Library of Science
Short Talk: Public Library of Science
7:00 - 8:00 PM Social Hour Peaks 14-16
7:30 - 10:00 PM Poster Session 2 Peaks 14-16
Sunday, January 11
7:00 - 8:00 AM Breakfast Peaks 6-12
8:00 - 11:00 AM Inherited Variation in Gene Expression (Joint) Peaks 4-5
* Leonid Kruglyak, Princeton University
Regulatory Variation in Yeast
Kevin P. White, Yale University School of Medicine
Evolution of Gene Expression in Drosophila
Stephanie Monks, University of Washington-Seattle/Rosetta Inpharmatics LLC
The Genetics of Gene Expression in Mice
Justin Fay, Washington University
Short Talk: Genetic Variation in Gene Expression is Associated with Phenotypic Variation Sequence Divergence
Matt Rockman, Duke University
Short Talk: Cis-Regulated Polymorphism: Evolution, Natural Variation, and Common Disease
9:20 - 9:40 AM Coffee Break Foyer
11:00 AM - 1:00 PM Poster Setup Peaks 14-16
1:00 - 10:00 PM Poster Viewing Peaks 14-16
4:30 - 5:00 PM Coffee & Snacks Available Foyer
5:00 - 7:00 PM Genetic Architecture of Human Disease Peaks 4-5
* Lon Cardon, University of Oxford
Stephen J. O'Brien, National Cancer Institute, National Institutes of Health
Architecture of Disease: Lessons from HIV Resistance
Nicholas Katsanis, Johns Hopkins School of Medicine
Modeling Oligogenic Disorders
John A. Phillips, Vanderbilt University School of Medicine
Short Talk: PPH is a Complex Disease Caused by Rare and Common Variants
Hua Tang, University of Chicago
Short Talk: Genetic Diseases and Natural Selection in Human
Örjan Carlborg, Roslin Institute
Short Talk: The Use of Epistasis in Genetic Dissection of Complex Traits
7:00 - 8:00 PM Social Hour Peaks 14-16
7:30 - 10:00 PM Poster Session 3 Peaks 14-16
Monday, January 12
7:00 - 8:00 AM Breakfast Peaks 6-12
8:00 - 11:00 AM Genetic Determinants of Common Disease Peaks 4-5
* Francis S. Collins, NHGRI, National Institutes of Health
Richard P. Lifton, Yale University School of Medicine
Genetic Dissection of Hypertension
Gilles Thomas, NCI - National Institutes of Health
The Genetics of CARD15, a Susceptibility Gene for an Inflammatory Bowel Disease
David M. Altshuler, Massachusetts General Hospital
Genetic Analysis of Diabetes
David Hunter, Harvard Medical School
Gene-Environment Interactions
9:20 - 9:40 AM Coffee Break Foyer
4:30 - 5:00 PM Coffee & Snacks Available Foyer
5:00 - 7:00 PM Application to Biology, Medicine and Society Peaks 4-5
* Richard P. Lifton, Yale University School of Medicine
Georgia Dunston, Howard University
The GRAD Biobank: A Resource for Exploring Genome Variation and Environment Interaction in Common Complex Diseases
Klaus Lindpaintner, F. Hoffmann-La Roche AG
Pharmacogenetics: A Realistic View
Francis S. Collins, NHGRI, National Institutes of Health
Applying Genetics to Medicine and Society
7:00 - 8:00 PM Social Hour Peaks 14-16
8:00 - 11:00 PM Entertainment Peaks 4-5
Tuesday, January 13
Departure
*Session Chair   †Speaker invited, not yet responded.



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