A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search  Andrea Angius, Enrico Petretto, Giovanni Battista.

Slides:



Advertisements
Similar presentations
A Susceptibility Locus for Migraine with Aura, on Chromosome 4q24
Advertisements

Genome Scan for Predisposing Loci for Distal Interphalangeal Joint Osteoarthritis: Evidence for a Locus on 2q  Jenni Leppävuori, Urho Kujala, Jaakko Kinnunen,
The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23
Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q  Alex Desautels, Gustavo Turecki, Jacques Montplaisir, Adolfo.
Transmission/Disequilibrium Tests for Extended Marker Haplotypes
Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata  Amalia Martinez-Mir, Abraham Zlotogorski, Derek Gordon,
Harald H.H. Göring, Joseph D. Terwilliger 
Genetic Linkage of Paget Disease of the Bone to Chromosome 18q
Genetic Linkage of the Muckle-Wells Syndrome to Chromosome 1q44
Robustness and Power of the Maximum-Likelihood–Binomial and Maximum-Likelihood– Score Methods, in Multipoint Linkage Analysis of Affected-Sibship Data 
Localization of a Gene (MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43  N.A. Alam, S. Bevan, M. Churchman, E.
Use of Homozygosity Mapping to Identify a Region on Chromosome 1 Bearing a Defective Gene That Causes Autosomal Recessive Homozygous Hypercholesterolemia.
Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype  Karen M. Cerosaletti, Ethan Lange, Heather.
Genomewide Scan in German Families Reveals Evidence for a Novel Psoriasis- Susceptibility Locus on Chromosome 19p13  Young-Ae Lee, Franz Rüschendorf, Christine.
Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11  Andrea Richter,
Soraya Beiraghi, Swapan K. Nath, Matthew Gaines, Desh D
Frances Busfield, David L. Duffy, Janine B. Kesting, Shelley M
Genomewide Linkage Scan Identifies a Novel Susceptibility Locus for Restless Legs Syndrome on Chromosome 9p  Shenghan Chen, William G. Ondo, Shaoqi Rao,
An Autosomal Dominant Thrombocytopenia Gene Maps to Chromosomal Region 10p  Anna Savoia, Maria Del Vecchio, Antonio Totaro, Silverio Perrotta, Giovanni.
Meta-analysis of Genetic-Linkage Analysis of Quantitative-Trait Loci
The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23
Tamara Rogers, David Chandler, Dora Angelicheva, P. K
Use of Closely Related Affected Individuals for the Genetic Study of Complex Diseases in Founder Populations  C. Bourgain, E. Génin, P. Holopainen, K.
The Gene for Severe Combined Immunodeficiency Disease in Athabascan-Speaking Native Americans Is Located on Chromosome 10p  Lanying Li, Dennis Drayna,
The American Journal of Human Genetics 
Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11  Mauricio Arcos-Burgos, F. Xavier.
Identification of a Genetic Locus for Ichthyosis Vulgaris on Chromosome 10q22.3– q24.2  Ping Liu, Qingyu Yang, Xu Wang, Aiping Feng, Tao Yang, Rong Yang,
Fine Mapping of the Split-Hand/Split-Foot Locus (SHFM3) at 10q24: Evidence for Anticipation and Segregation Distortion  Rýdvan S. Özen, Bora E. Baysal,
Susceptibility Loci for Preeclampsia on Chromosomes 2p25 and 9p13 in Finnish Families  Hannele Laivuori, Päivi Lahermo, Vesa Ollikainen, Elisabeth Widen,
Howard B. Yeon, Noralane M. Lindor, J.G. Seidman, Christine E. Seidman 
John D. Rioux, Valerie A. Stone, Mark J
Tristan F. W. McMullan, Andrew R. Collins, Anthony G. Tyers, David O
Familial Juvenile Hyperuricemic Nephropathy: Localization of the Gene on Chromosome 16p11.2—and Evidence for Genetic Heterogeneity  Blanka Stibůrková,
A Locus for Hereditary Sensory Neuropathy with Cough and Gastroesophageal Reflux on Chromosome 3p22-p24  C. Kok, M.L. Kennerson, P.J. Spring, A.J. Ing,
Genetic and Mutational Analyses of a Large Multiethnic Bardet-Biedl Cohort Reveal a Minor Involvement of BBS6 and Delineate the Critical Intervals of.
Localization of a Gene for Benign Adult Familial Myoclonic Epilepsy to Chromosome 8q23.3-q24.1  Masaaki Mikami, Takeshi Yasuda, Akira Terao, Masayuki.
A Major Predisposition Locus for Severe Obesity, at 4p15-p14
Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating Neuropathies  Valerie A. Street, Jeff D. Goldy,
Claus Skaanning Jensen, Augustine Kong 
Koji Suzuki, Tania Bustos, Richard A. Spritz 
Erratum The American Journal of Human Genetics
Linkage Analysis Identifies a Novel Locus for Restless Legs Syndrome on Chromosome 2q in a South Tyrolean Population Isolate  Irene Pichler, Fabio Marroni,
Linkage Analysis of X-linked Cone-Rod Dystrophy: Localization to Xp11
Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13 
On a Randomization Procedure in Linkage Analysis
Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12- q12 and Evidence for Further Genetic Heterogeneity  Judith Fischer, Alexandra.
Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a.
John A. Martignetti, Karen E
A Severely Affected Male Born into a Rett Syndrome Kindred Supports X-Linked Inheritance and Allows Extension of the Exclusion Map  Carolyn Schanen, Uta.
Genomewide Scan in Families with Schizophrenia from the Founder Population of Afrikaners Reveals Evidence for Linkage and Uniparental Disomy on Chromosome.
Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11.
Suzanne M. Leal, Jurg Ott  The American Journal of Human Genetics 
A Genomewide Search Using an Original Pairwise Sampling Approach for Large Genealogies Identifies a New Locus for Total and Low-Density Lipoprotein Cholesterol.
Linkage Analysis in a Large Brazilian Family with van der Woude Syndrome Suggests the Existence of a Susceptibility Locus for Cleft Palate at 17p  
Hereditary Isolated Renal Magnesium Loss Maps to Chromosome 11q23
Familial Nontoxic Multinodular Thyroid Goiter Locus Maps to Chromosome 14q but Does Not Account for Familial Nonmedullary Thyroid Cancer  Graham R. Bignell,
A New Locus for Autosomal Recessive Hypercholesterolemia Maps to Human Chromosome 15q25-q26  Milco Ciccarese, Adolfo Pacifico, Giancarlo Tonolo, Paolo.
Mapping of the Major Psoriasis-Susceptibility Locus (PSORS1) in a 70-Kb Interval around the Corneodesmosin Gene (CDSN)  Sandro Orrù, Erika Giuressi, Carlo.
Volume 53, Issue 6, Pages (June 1998)
A Gene for an Autosomal Dominant Scleroatrophic Syndrome Predisposing to Skin Cancer (Huriez Syndrome) Maps to Chromosome 4q23  Young-Ae Lee, Howard P.
Identification of a New Candidate Locus for Uric Acid Nephrolithiasis
A New Familial Amyotrophic Lateral Sclerosis Locus on Chromosome 16q12
Detection and Integration of Genotyping Errors in Statistical Genetics
Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping  Bru Cormand, Kristiina Avela, Helena Pihko,
Sanjay Shete, Xiaojun Zhou, Christopher I. Amos 
Kung-Yee Liang, Fang-Chi Hsu, Terri H. Beaty, Kathleen C. Barnes 
Minimum-Recombinant Haplotyping in Pedigrees
A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1,Maps to Chromosome 12p13  I.A. Meijer, C.K. Hand, K.K. Grewal, M.G. Stefanelli, E.J. Ives,
Gonçalo R. Abecasis, Janis E. Wigginton 
Mapping of a New SGBS Locus to Chromosome Xp22 in a Family with a Severe Form of Simpson-Golabi-Behmel Syndrome  L.M. Brzustowicz, S. Farrell, M.B. Khan,
Presentation transcript:

A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search  Andrea Angius, Enrico Petretto, Giovanni Battista Maestrale, Paola Forabosco, Giuseppina Casu, Daniela Piras, Manuela Fanciulli, Mario Falchi, Paola Maria Melis, Mario Palermo, Mario Pirastu  The American Journal of Human Genetics  Volume 71, Issue 4, Pages 893-905 (October 2002) DOI: 10.1086/342929 Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 1 Twelve-generation pedigree used in the linkage and Simwalk2 analyses. Because of computational constraints, the pedigree was broken into four smaller branches, as indicated in the figure. Family members analyzed in stage I are indicated by arrows. Blackened symbols denote affected individuals. The American Journal of Human Genetics 2002 71, 893-905DOI: (10.1086/342929) Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 2 Nonparametric statistics estimated by SimWalk2 (Sobel and Lange 1996). Statistic A is the number of different founder alleles contributing alleles to the affected individuals. Statistic B is the maximum number of alleles among the affected individuals descended from any one founder allele. Statistic C is the “entropy” of the marker alleles among the affected individuals. Statistic D is the extent of allele sharing among all affected pairs, as measured by their IBD kinship coefficient. Statistic E is the “NPL_all” statistic, as implemented in GeneHunter. The American Journal of Human Genetics 2002 71, 893-905DOI: (10.1086/342929) Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 3 Statistic D results for each analyzed branch of the pedigree in the whole region shown in figure 2 The American Journal of Human Genetics 2002 71, 893-905DOI: (10.1086/342929) Copyright © 2002 The American Society of Human Genetics Terms and Conditions