| Estimation of fixation indices and gene diversities | Annals of Human Genetics | 1983 | 730 |
| Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy | Human Genetics | 1983 | 475 |
| The human serum paraoxonase/arylesterase polymorphism | American Journal of Human Genetics | 1983 | 454 |
| A unified model for complex segregation analysis | American Journal of Human Genetics | 1983 | 349 |
| The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism | Human Genetics | 1983 | 330 |
| The chromosome constitution of 1000 human spermatozoa | Human Genetics | 1983 | 208 |
| Eukaryotic DNA methylation | Human Genetics | 1983 | 178 |
| Linkage analysis and family classification under heterogeneity | Annals of Human Genetics | 1983 | 169 |
| The transmission of schizophrenia under a multifactorial threshold model | American Journal of Human Genetics | 1983 | 163 |
| The blepharophimosis, ptosis, and epicanthus inversus syndrome: delineation of two types | American Journal of Human Genetics | 1983 | 160 |
| The human serum paraoxonase polymorphism: identification of phenotypes by their response to salts | American Journal of Human Genetics | 1983 | 156 |
| X-linked dominant inherited diseases with lethality in hemizygous males | Human Genetics | 1983 | 143 |
| Meiotic studies in a series of 1100 infertile and sterile males | Human Genetics | 1983 | 116 |
| Nucleolus organizer regions and nucleoli | Human Genetics | 1983 | 115 |
| The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families | Human Genetics | 1983 | 112 |
| Sex ratio in spontaneous abortions | Annals of Human Genetics | 1983 | 110 |
| Cytologic evidence for three human X-chromosomal segments escaping inactivation | Human Genetics | 1983 | 106 |
| The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age | American Journal of Human Genetics | 1983 | 103 |
| Population genetic studies on aldehyde dehydrogenase isozyme deficiency and alcohol sensitivity | American Journal of Human Genetics | 1983 | 103 |
| Plasma paraoxonase polymorphism: a new enzyme assay, population, family, biochemical, and linkage studies | American Journal of Human Genetics | 1983 | 99 |
| The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity | American Journal of Human Genetics | 1983 | 99 |
| Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies | Human Genetics | 1983 | 94 |
| Down's syndrome in the male. Reproductive pathology and meiotic studies | Human Genetics | 1983 | 91 |
| Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases | Human Genetics | 1983 | 87 |
| Juvenile idiopathic haemochromatosis: a life-threatening disorder presenting as hypogonadotropic hypogonadism | Human Genetics | 1983 | 86 |
