Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Cutting a Gordian knot in the linkage analysis of complex human traits.

Authors: J Ott; H G Schrott; J L Goldstein; W R Hazzard; F H Allen; C T Falk; A G Motulsky
Journal: Am J Hum Genet Date: 1974-09 Impact factor: 11.025

10. Predisposition to familial osteoarthrosis linked to type II collagen gene.

Authors: A Palotie; P Väisänen; J Ott; L Ryhänen; K Elima; M Vikkula; K Cheah; E Vuorio; L Peltonen
Journal: Lancet Date: 1989-04-29 Impact factor: 79.321

8 in total

1. Replication of linkage studies of complex traits: an examination of variation in location estimates.

Authors: S B Roberts; C J MacLean; M C Neale; L J Eaves; K S Kendler
Journal: Am J Hum Genet Date: 1999-09 Impact factor: 11.025

2. Genetic Epidemiology of Complex Phenotypes.

Authors: Darren D O'Rielly; Proton Rahman
Journal: Methods Mol Biol Date: 2021

3. Association versus linkage studies in psychosis genetics.

Authors: M M Nöthen; P Propping; R Fimmers
Journal: J Med Genet Date: 1993-08 Impact factor: 6.318

4. Family studies of non-insulin-dependent diabetes mellitus in South Indians.

Authors: M I McCarthy; G A Hitman; D C Shields; N E Morton; C Snehalatha; V Mohan; A Ramachandran; M Viswanathan
Journal: Diabetologia Date: 1994-12 Impact factor: 10.122

5. Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.

Authors: W P Whitehouse; M Rees; D Curtis; A Sundqvist; K Parker; E Chung; D Baralle; R M Gardiner
Journal: Am J Hum Genet Date: 1993-09 Impact factor: 11.025

Cutting a Gordian knot in the linkage analysis of complex human traits.

1. SCHIZOPHRENIA AS A GENETIC MORPHISM.

2. The simulation of mendelism.

3. The genetical background of common diseases.

4. Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.

5. The affected-pedigree-member method of linkage analysis.

6. Genetics of common disorders.

7. Linkage between familial hypercholesterolemia with xanthomatosis and the C3 polymorphism confirmed.

8. A comparison of three affected-sib-pair scoring methods to detect HLA-linked disease susceptibility genes.

9. Linkage studies in a large kindred with familial hypercholesterolemia.

10. Predisposition to familial osteoarthrosis linked to type II collagen gene.

1. Replication of linkage studies of complex traits: an examination of variation in location estimates.

2. Genetic Epidemiology of Complex Phenotypes.

3. Association versus linkage studies in psychosis genetics.

4. Family studies of non-insulin-dependent diabetes mellitus in South Indians.

5. Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.

6. Mathematical limits of multilocus models: the genetic transmission of bipolar disorder.

Review 7. Identification of the phenotype in psychiatric genetics.

8. Absence of linkage between familial neural tube defects and PAX3 gene.