Published in Am J Hum Genet on December 01, 1986
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. Am J Hum Genet (1986) 3.83
A test of the heterozygote-advantage hypothesis in cystic fibrosis carriers. Am J Hum Genet (1988) 1.03
Genetic markers on chromosome 7. J Med Genet (1988) 0.95
Comparative map for mice and humans. Mamm Genome (1991) 0.81
Cystic fibrosis. West J Med (1988) 0.75
Human carboxypeptidase A identifies a BglII RFLP and maps to 7q31-qter. Am J Hum Genet (1990) 0.75
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. Am J Hum Genet (1986) 3.83
Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data. Am J Hum Genet (1986) 3.16
Structure of two related rat pancreatic trypsin genes. J Biol Chem (1984) 2.24
A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes. Am J Hum Genet (1985) 2.12
High resolution of human evolutionary trees with polymorphic microsatellites. Nature (1994) 28.48
Evolution at two levels in humans and chimpanzees. Science (1975) 21.07
Phylogenetic analysis. Models and estimation procedures. Am J Hum Genet (1967) 17.65
Linkage of early-onset familial breast cancer to chromosome 17q21. Science (1990) 16.21
Multilocus genotypes, a tree of individuals, and human evolutionary history. Am J Hum Genet (1997) 14.46
Identification of a RING protein that can interact in vivo with the BRCA1 gene product. Nat Genet (1996) 12.96
Genetic absolute dating based on microsatellites and the origin of modern humans. Proc Natl Acad Sci U S A (1995) 9.25
An evaluation of genetic distances for use with microsatellite loci. Genetics (1995) 8.79
Population structure and human evolution. Proc R Soc Lond B Biol Sci (1966) 8.78
Y chromosome sequence variation and the history of human populations. Nat Genet (2000) 8.34
Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. Proc Natl Acad Sci U S A (1991) 8.14
A randomized trial of surgery in the treatment of single metastases to the brain. N Engl J Med (1990) 7.92
Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns. J Mol Evol (1983) 6.80
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res (1997) 6.73
The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective. Science (2000) 6.57
Postoperative radiotherapy in the treatment of single metastases to the brain: a randomized trial. JAMA (1998) 6.49
Cultural transmission and evolution: a quantitative approach. Monogr Popul Biol (1981) 6.42
The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations. Ann Hum Genet (2001) 6.24
The probability of consanguineous marriages. Genetics (1966) 5.85
Genetic evidence for a higher female migration rate in humans. Nat Genet (1998) 5.77
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. Cytogenet Cell Genet (1989) 5.48
Nuclear DNA polymorphism in a Mandenka population from Senegal: comparison with eight other human populations. Ann Hum Genet (1995) 5.34
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome. J Clin Invest (2000) 5.12
A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet (1999) 4.96
A migration matrix model for the study of random genetic drift. Genetics (1968) 4.59
A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history. Proc Natl Acad Sci U S A (1996) 4.52
Comparison of 79 DNA polymorphisms tested in Australians, Japanese and Papua New Guineans with those of five other human populations. Gene Geogr (1994) 4.50
BRCA1 is secreted and exhibits properties of a granin. Nat Genet (1996) 4.26
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nat Genet (1994) 4.15
Structure of a BRCA1-BARD1 heterodimeric RING-RING complex. Nat Struct Biol (2001) 4.15
Theory and observation in cultural transmission. Science (1982) 4.05
Study of 47 DNA markers in five populations from four continents. Gene Geogr (1987) 4.04
Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families. Proc Natl Acad Sci U S A (1988) 4.02
Closing in on a breast cancer gene on chromosome 17q. Am J Hum Genet (1992) 3.89
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. Am J Hum Genet (1986) 3.83
Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk. Circulation (1990) 3.83
Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA. Proc Natl Acad Sci U S A (1981) 3.71
The C-terminal (BRCT) domains of BRCA1 interact in vivo with CtIP, a protein implicated in the CtBP pathway of transcriptional repression. J Biol Chem (1998) 3.67
The functional and regulatory roles of sigma factors in transcription. Cold Spring Harb Symp Quant Biol (1998) 3.63
Transient confinement of a glycosylphosphatidylinositol-anchored protein in the plasma membrane. Biochemistry (1997) 3.59
Demographic history of India and mtDNA-sequence diversity. Am J Hum Genet (1995) 3.47
Growth retardation and tumour inhibition by BRCA1. Nat Genet (1996) 3.47
Well-being and treatment satisfaction in older people with diabetes. Diabetes Care (1998) 3.31
Population genetics of BRCA1 and BRCA2. Am J Hum Genet (1997) 3.28
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous. Science (1997) 3.21
Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level. Am J Hum Genet (1986) 3.17
Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data. Am J Hum Genet (1986) 3.16
An apportionment of human DNA diversity. Proc Natl Acad Sci U S A (1997) 3.15
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man. Proc Natl Acad Sci U S A (1983) 3.07
Inference of human evolution through cladistic analysis of nuclear DNA restriction polymorphisms. Proc Natl Acad Sci U S A (1994) 3.07
BRCA1 and BRCA2 and the genetics of breast and ovarian cancer. Hum Mol Genet (2001) 2.98
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study. Am J Hum Genet (1996) 2.97
Protein lateral mobility as a reflection of membrane microstructure. Bioessays (1993) 2.91
Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1. Genome Res (1996) 2.91
Frequency of breast cancer attributable to BRCA1 in a population-based series of American women. JAMA (1998) 2.76
The Manchester Royal Infirmary Programmed Investigation Unit. Br Med J (1973) 2.74
Clinical assessment of HIV-associated lipodystrophy in an ambulatory population. AIDS (2001) 2.73
Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins. J Virol (1997) 2.64
Parents' accounts of obtaining a diagnosis of childhood cancer. Lancet (2001) 2.62
Population genetic implications from sequence variation in four Y chromosome genes. Proc Natl Acad Sci U S A (2000) 2.62
Cultural versus biological inheritance: phenotypic transmission from parents to children. (A theory of the effect of parental phenotypes on children's phenotypes). Am J Hum Genet (1973) 2.61
Assortment of encounters and evolution of cooperativeness. Proc Natl Acad Sci U S A (1982) 2.60
Uralic genes in Europe. Am J Phys Anthropol (1990) 2.57
Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies. Neurology (2000) 2.48
Construction of human Y-chromosomal haplotypes using a new polymorphic A to G transition. Hum Mol Genet (1994) 2.47
Predictors of poor neurologic outcome after induced mild hypothermia following cardiac arrest. Neurology (2008) 2.44
Concordance for type 2 (non-insulin-dependent) diabetes mellitus in male twins. Diabetologia (1987) 2.44
Risk of breast cancer to relatives of young breast cancer patients. J Natl Cancer Inst (1985) 2.43
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science (1998) 2.42
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21. Am J Hum Genet (1993) 2.37
Choosing and using services for sexual health: a qualitative study of women's views. Sex Transm Infect (2001) 2.36
Cultural variation in Africa: role of mechanisms of transmission and adaptation. Proc Natl Acad Sci U S A (1995) 2.35
Genetic epidemiology of breast cancer and associated cancers in high-risk families. I. Segregation analysis. J Natl Cancer Inst (1983) 2.21
The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations. Am J Hum Genet (2004) 2.20
Analysis of evolution: evolutionary rates, independence and treeness. Theor Popul Biol (1975) 2.15
Detection of genetic variation with radioactive ligands. III. genetic polymorphism of transcobalamin II in human plasma. Am J Hum Genet (1978) 2.13
Cultural and biological evolutionary processes, selection for a trait under complex transmission. Theor Popul Biol (1976) 2.13
A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes. Am J Hum Genet (1985) 2.12
Insights into the functions of BRCA1 and BRCA2. Trends Genet (2000) 2.10
Association mapping of disease loci, by use of a pooled DNA genomic screen. Am J Hum Genet (1997) 2.07
Statistical properties of the variation at linked microsatellite loci: implications for the history of human Y chromosomes. Mol Biol Evol (1996) 2.07
Analytic review: some current problems of human population genetics. Am J Hum Genet (1973) 2.05
Comparative virulence of respiratory syncytial virus subgroups A and B. Lancet (1989) 2.03
Study of an additional 58 DNA markers in five human populations from four continents. Gene Geogr (1991) 1.98
Pseudolinkage of the duplicate loci for supernatant aspartate aminotransferase in brook trout, Salvelinus fontinalis. J Hered (1980) 1.97
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree. Nature (1988) 1.96
Paradox of the evolution of communication and of social interactivity. Proc Natl Acad Sci U S A (1983) 1.95
Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis. Am J Hum Genet (1997) 1.94
The genetics of psoriasis: a complex disorder of the skin and immune system. Hum Mol Genet (1998) 1.94
Cultural versus genetic adaptation. Proc Natl Acad Sci U S A (1983) 1.93
The socio-economic impact of telehealth: a systematic review. J Telemed Telecare (2003) 1.93
Alterations in the Young's modulus and volumetric properties of chondrocytes isolated from normal and osteoarthritic human cartilage. J Biomech (1999) 1.91
Identification of Id4 as a regulator of BRCA1 expression by using a ribozyme-library-based inverse genomics approach. Proc Natl Acad Sci U S A (2001) 1.90
Partnerships with children. BMJ (1999) 1.89
Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q. Nat Genet (1994) 1.88
Inherited breast and ovarian cancer. Hum Mol Genet (1995) 1.87
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet (1992) 1.87