| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Confidence-Set Approach for Finding Tightly Linked Genomic Regions
|
Lin, Shili
|
|
2001
|
68 |
5 |
p. 1219-1228
10 p.
|
artikel
|
| 2 |
A Major Locus for Fasting Insulin Concentrations and Insulin Resistance on Chromosome 6q with Strong Pleiotropic Effects on Obesity-Related Phenotypes in Nondiabetic Mexican Americans
|
Duggirala, Ravindranath
|
|
2001
|
68 |
5 |
p. 1149-1164
16 p.
|
artikel
|
| 3 |
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, Emory University School of Medicine, 1462 Clifton Road, Room B28, 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.
|
|
|
2001
|
68 |
5 |
p. 1308-1312
5 p.
|
artikel
|
| 4 |
Broad and Narrow Heritabilities of Quantitative Traits in a Founder Population
|
Abney, Mark
|
|
2001
|
68 |
5 |
p. 1302-1307
6 p.
|
artikel
|
| 5 |
Characterization of Mutations in the CPO Gene in British Patients Demonstrates Absence of Genotype-Phenotype Correlation and Identifies Relationship between Hereditary Coproporphyria and Harderoporphyria
|
Lamoril, Jérôme
|
|
2001
|
68 |
5 |
p. 1130-1138
9 p.
|
artikel
|
| 6 |
Complexity and Power in Case-Control Association Studies
|
Longmate, Jeffrey A.
|
|
2001
|
68 |
5 |
p. 1229-1237
9 p.
|
artikel
|
| 7 |
Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome
|
Buiting, Karin
|
|
2001
|
68 |
5 |
p. 1290-1294
5 p.
|
artikel
|
| 8 |
Erratum
|
|
|
2001
|
68 |
5 |
p. 1313-
1 p.
|
artikel
|
| 9 |
Heteroplasmy of the Human mtDNA Control Region Remains Constant during Life
|
Lagerström-Fermér, Maria
|
|
2001
|
68 |
5 |
p. 1299-1301
3 p.
|
artikel
|
| 10 |
Identification and Expression Analysis of Spastin Gene Mutations in Hereditary Spastic Paraplegia
|
Svenson, Ingrid K.
|
|
2001
|
68 |
5 |
p. 1077-1085
9 p.
|
artikel
|
| 11 |
Identification of a New Candidate Locus for Uric Acid Nephrolithiasis
|
Ombra, Maria Neve
|
|
2001
|
68 |
5 |
p. 1119-1129
11 p.
|
artikel
|
| 12 |
International Collaboration Provides Convincing Linkage Replication in Complex Disease through Analysis of a Large Pooled Data Set: Crohn Disease and Chromosome 16
|
Cavanaugh, Juleen
|
|
2001
|
68 |
5 |
p. 1165-1171
7 p.
|
artikel
|
| 13 |
Linkage and Association Analysis of Angiotensin I–Converting Enzyme (ACE)–Gene Polymorphisms with ACE Concentration and Blood Pressure
|
Zhu, Xiaofeng
|
|
2001
|
68 |
5 |
p. 1139-1148
10 p.
|
artikel
|
| 14 |
Localization of a Gene (MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43
|
Alam, N.A.
|
|
2001
|
68 |
5 |
p. 1264-1269
6 p.
|
artikel
|
| 15 |
Localization of the Gene for Distal Hereditary Motor Neuronopathy VII (dHMN-VII) to Chromosome 2q14
|
McEntagart, Meriel
|
|
2001
|
68 |
5 |
p. 1270-1276
7 p.
|
artikel
|
| 16 |
MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin
|
Trappe, R.
|
|
2001
|
68 |
5 |
p. 1093-1101
9 p.
|
artikel
|
| 17 |
Model-Free Linkage Analysis with Covariates Confirms Linkage of Prostate Cancer to Chromosomes 1 and 4
|
Goddard, Katrina A.B.
|
|
2001
|
68 |
5 |
p. 1197-1206
10 p.
|
artikel
|
| 18 |
Mortality in Neurofibromatosis 1: An Analysis Using U.S. Death Certificates
|
Rasmussen, Sonja A.
|
|
2001
|
68 |
5 |
p. 1110-1118
9 p.
|
artikel
|
| 19 |
Null RPGRIP1 Alleles in Patients with Leber Congenital Amaurosis
|
Dryja, Thaddeus P.
|
|
2001
|
68 |
5 |
p. 1295-1298
4 p.
|
artikel
|
| 20 |
Paternal Uniparental Isodisomy of Chromosome 20q—and the Resulting Changes in GNAS1 Methylation—as a Plausible Cause of Pseudohypoparathyroidism
|
Bastepe, Murat
|
|
2001
|
68 |
5 |
p. 1283-1289
7 p.
|
artikel
|
| 21 |
Recent Origin and Spread of a Common Lithuanian Mutation, G197del LDLR, Causing Familial Hypercholesterolemia: Positive Selection Is Not Always Necessary to Account for Disease Incidence among Ashkenazi Jews
|
Durst, Ronen
|
|
2001
|
68 |
5 |
p. 1172-1188
17 p.
|
artikel
|
| 22 |
Regression Models for Linkage Heterogeneity Applied to Familial Prostate Cancer
|
Schaid, Daniel J.
|
|
2001
|
68 |
5 |
p. 1189-1196
8 p.
|
artikel
|
| 23 |
Segregation Analyses of 1,476 Population-Based Australian Families Affected by Prostate Cancer
|
Cui, Jisheng
|
|
2001
|
68 |
5 |
p. 1207-1218
12 p.
|
artikel
|
| 24 |
The Primary Erythermalgia–Susceptibility Gene Is Located on Chromosome 2q31-32
|
Drenth, Joost P.H.
|
|
2001
|
68 |
5 |
p. 1277-1282
6 p.
|
artikel
|
| 25 |
This Month in the Journal
|
Beauregard, Kathryn
|
|
2001
|
68 |
5 |
p. i-ii
nvt p.
|
artikel
|
| 26 |
Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway
|
Verhoeven, Nanda M.
|
|
2001
|
68 |
5 |
p. 1086-1092
7 p.
|
artikel
|
| 27 |
Transformation of Sib-Pair Values for the Haseman-Elston Method
|
Wang, Daolong
|
|
2001
|
68 |
5 |
p. 1238-1249
12 p.
|
artikel
|
| 28 |
Transmission/Disequilibrium Test Meets Measured Haplotype Analysis: Family-Based Association Analysis Guided by Evolution of Haplotypes
|
Seltman, Howard
|
|
2001
|
68 |
5 |
p. 1250-1263
14 p.
|
artikel
|
| 29 |
Up-Regulation of WNT-4 Signaling and Dosage-Sensitive Sex Reversal in Humans
|
Jordan, Brian K.
|
|
2001
|
68 |
5 |
p. 1102-1109
8 p.
|
artikel
|
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