no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution
|
Otto, Edgar |
|
2002 |
71 |
5 |
p. 1161-1167 7 p. |
article |
2 |
A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)
|
Reid, Evan |
|
2002 |
71 |
5 |
p. 1189-1194 6 p. |
article |
3 |
Alcohol Dehydrogenase and Alcohol Dependence: Variation in Genotype-Associated Risk between Populations
|
Whitfield, John B. |
|
2002 |
71 |
5 |
p. 1247-1250 4 p. |
article |
4 |
A Major Susceptibility Locus for Systemic Lupus Erythemathosus Maps to Chromosome 1q31
|
Johanneson, Bo |
|
2002 |
71 |
5 |
p. 1060-1071 12 p. |
article |
5 |
Announcements 1 1 Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please mail announcements to The American Journal of Human Genetics, Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Room 301, Atlanta, GA 30322-3050; fax them to (404) 712-9984; or send via E-mail to ajhg@emory.edu. Submission must be received at least 7 weeks before the month of issue in which publication is requested. They must be double spaced with a 1½-inch margin on all sides. The maximum length is 250 words, excluding the address for correspondence. Please include a cover letter indicating the name of the sponsoring ASHG member.
|
|
|
2002 |
71 |
5 |
p. 1256-1257 2 p. |
article |
6 |
A Nonsense Mutation in CRYBB1 Associated with Autosomal Dominant Cataract Linked to Human Chromosome 22q
|
Mackay, Donna S. |
|
2002 |
71 |
5 |
p. 1216-1221 6 p. |
article |
7 |
A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group
|
Brody, Lawrence C. |
|
2002 |
71 |
5 |
p. 1207-1215 9 p. |
article |
8 |
Detecting Polymorphisms and Mutations in Candidate Genes
|
Collins, Julianne S. |
|
2002 |
71 |
5 |
p. 1251-1252 2 p. |
article |
9 |
Distribution of Recombination Crossovers and the Origin of Haplotype Blocks: The Interplay of Population History, Recombination, and Mutation
|
Wang, Ning |
|
2002 |
71 |
5 |
p. 1227-1234 8 p. |
article |
10 |
Duane Radial Ray Syndrome (Okihiro Syndrome) Maps to 20q13 and Results from Mutations in SALL4, a New Member of the SAL Family
|
Al-Baradie, Raidah |
|
2002 |
71 |
5 |
p. 1195-1199 5 p. |
article |
11 |
Erratum
|
|
|
2002 |
71 |
5 |
p. 1258- 1 p. |
article |
12 |
Erratum
|
|
|
2002 |
71 |
5 |
p. 1258- 1 p. |
article |
13 |
Erratum
|
|
|
2002 |
71 |
5 |
p. 1258- 1 p. |
article |
14 |
Erratum
|
|
|
2002 |
71 |
5 |
p. 1258- 1 p. |
article |
15 |
Evaluating the Results of Genomewide Linkage Scans of Complex Traits by Locus Counting
|
Wiltshire, Steven |
|
2002 |
71 |
5 |
p. 1175-1182 8 p. |
article |
16 |
Evidence for Balancing Selection from Nucleotide Sequence Analyses of Human G6PD
|
Verrelli, Brian C. |
|
2002 |
71 |
5 |
p. 1112-1128 17 p. |
article |
17 |
Family-Based Association Tests Incorporating Parental Genotypes
|
Kraft, Peter |
|
2002 |
71 |
5 |
p. 1238-1239 2 p. |
article |
18 |
Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia
|
Crolla, John A. |
|
2002 |
71 |
5 |
p. 1138-1149 12 p. |
article |
19 |
Genetic, Linguistic and Archaeological Perspectives on Human Diversity in Southeast Asia
|
Quintana-Murci, Lluís |
|
2002 |
71 |
5 |
p. 1253-1255 3 p. |
article |
20 |
Genetic Proof of Unequal Meiotic Crossovers in Reciprocal Deletion and Duplication of 17p11.2
|
Shaw, Christine J. |
|
2002 |
71 |
5 |
p. 1072-1081 10 p. |
article |
21 |
Genomewide Linkage Analysis of Body Mass Index across 28 Years of the Framingham Heart Study
|
Atwood, Larry D. |
|
2002 |
71 |
5 |
p. 1044-1050 7 p. |
article |
22 |
Griscelli Syndrome Types 1 and 2
|
Ménasché, Gaël |
|
2002 |
71 |
5 |
p. 1237-1238 2 p. |
article |
23 |
Haplotype Inference in Random Population Samples
|
Lin, Shin |
|
2002 |
71 |
5 |
p. 1129-1137 9 p. |
article |
24 |
In Search of Geographical Patterns in European Mitochondrial DNA
|
Richards, Martin |
|
2002 |
71 |
5 |
p. 1168-1174 7 p. |
article |
25 |
Is the Transportation Highway the Right Road for Hereditary Spastic Paraplegia?
|
Crosby, Andrew H. |
|
2002 |
71 |
5 |
p. 1009-1016 8 p. |
article |
26 |
Maternal Genetic Effects, Exerted by Genes Involved in Homocysteine Remethylation, Influence the Risk of Spina Bifida
|
Doolin, Marie-Therese |
|
2002 |
71 |
5 |
p. 1222-1226 5 p. |
article |
27 |
Multiple Hits during Early Embryonic Development: Digenic Diseases and Holoprosencephaly
|
Ming, Jeffrey E. |
|
2002 |
71 |
5 |
p. 1017-1032 16 p. |
article |
28 |
Mutation in Human Desmoplakin Domain Binding to Plakoglobin Causes a Dominant Form of Arrhythmogenic Right Ventricular Cardiomyopathy
|
Rampazzo, Alessandra |
|
2002 |
71 |
5 |
p. 1200-1206 7 p. |
article |
29 |
Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome
|
Beltrán-Valero de Bernabé, Daniel |
|
2002 |
71 |
5 |
p. 1033-1043 11 p. |
article |
30 |
Partition-Ligation–Expectation-Maximization Algorithm for Haplotype Inference with Single-Nucleotide Polymorphisms
|
Qin, Zhaohui S. |
|
2002 |
71 |
5 |
p. 1242-1247 6 p. |
article |
31 |
Regarding “Parental Genotypes in the Risk of a Complex Disease”
|
Weinberg, Clarice R. |
|
2002 |
71 |
5 |
p. 1239-1240 2 p. |
article |
32 |
Reply to Comments by Kraft and Wilson and by Weinberg and Mitchell on “Parental Genotypes in the Risk of a Complex Disease”
|
Labuda, Damian |
|
2002 |
71 |
5 |
p. 1240-1242 3 p. |
article |
33 |
Reply to Ménasché et al.
|
Huizing, Marjan |
|
2002 |
71 |
5 |
p. 1238- 1 p. |
article |
34 |
Reply to Whitfield
|
Kidd, Kenneth K. |
|
2002 |
71 |
5 |
p. 1250-1251 2 p. |
article |
35 |
RNA Binding Proteins: New Concepts in Gene Regulation
|
Danner, Dean J. |
|
2002 |
71 |
5 |
p. 1255- 1 p. |
article |
36 |
The DNA-Based Structure of Human Chromosome 5 in Interphase
|
Lemke, Johannes |
|
2002 |
71 |
5 |
p. 1051-1059 9 p. |
article |
37 |
The Fingerprint of Phantom Mutations in Mitochondrial DNA Data
|
Bandelt, Hans-Jürgen |
|
2002 |
71 |
5 |
p. 1150-1160 11 p. |
article |
38 |
The Making of the African mtDNA Landscape
|
Salas, Antonio |
|
2002 |
71 |
5 |
p. 1082-1111 30 p. |
article |
39 |
This Month in the Journal
|
Beauregard, Kathryn |
|
2002 |
71 |
5 |
p. i-ii nvt p. |
article |
40 |
Upward Bias in Estimation of Genetic Effects
|
Siegmund, D. |
|
2002 |
71 |
5 |
p. 1183-1188 6 p. |
article |
41 |
Using All Alleles in the Multiallelic Versions of the SDT and Combined SDT/TDT
|
Czika, Wendy |
|
2002 |
71 |
5 |
p. 1235-1236 2 p. |
article |