Published in Am J Hum Genet on May 01, 1966
STUDIES ON THE XAVANTE INDIANS OF THE BRAZILIAN MATO GROSSO. Am J Hum Genet (1964) 6.44
The blood groups and secretor types in five potentially fatal diseases of Caucasian children. Acta Genet Stat Med (1965) 1.78
Aspects of the Tecumseh study. Public Health Rep (1961) 1.48
The inheritance of blood groups. Br Med Bull (1959) 1.24
Blood group studies on the family of an XX/XY hermaphrodite with generalized tissue mosaicism. Am J Hum Genet (1963) 1.20
An epidemiological study in a total community: the Tecumseh project. Med Bull (Ann Arbor) (1960) 1.19
A human blood-group gene intermediate between M and N. Nature (1953) 1.18
AN ANOMALY OF INHERITANCE IN THE MNSS BLOOD GROUPS. Am J Hum Genet (1965) 1.00
Some new observations on the MN system. Vox Sang (1960) 0.91
Blood groups in man and lower primates: a review. Transfusion (1963) 0.83
Notes on some reactions of human anti-M and anti-N sera. Br J Haematol (1957) 0.83
The genetic structure of a tirbal population, the Vanomama Indians. II. Eleven blood-group systems and the ABH-Le secretor traits. Ann Hum Genet (1972) 4.87
Intratribal genetic differentiation among the Yanomama Indians of southern Venezuela. Proc Natl Acad Sci U S A (1967) 3.75
The NAS-NRC twin panel: methods of construction of the panel, zygosity diagnosis, and proposed use. Am J Hum Genet (1967) 2.81
The influence of cultural factors on the demography and pattern of gene flow from the Makiritare to the Yanomama Indians. Am J Phys Anthropol (1970) 2.59
Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease). Clin Genet (1971) 2.51
The genetic structure of a tribal population, the Yanomama Indians XI. Gene frequencies for 10 blood groups and the ABH-Le secretor traits in the Yanomama and their neighbors; the uniqueness of the tribe. Am J Hum Genet (1975) 2.28
Genetic characterization of Gainj- and Kalam-speaking peoples of Papua New Guinea. Am J Phys Anthropol (1986) 2.28
GM allotypes in Native Americans: evidence for three distinct migrations across the Bering land bridge. Am J Phys Anthropol (1985) 2.11
Absence of distal interphalangeal creases of fingers with flexion limitation. J Med Genet (1976) 2.05
Microevolution in lower Central America: genetic characterization of the Chibcha-speaking groups of Costa Rica and Panama, and a consensus taxonomy based on genetic and linguistic affinity. Am J Hum Genet (1990) 1.86
X-linked mental retardation and-or hydrocephalus. Clin Genet (1972) 1.81
The blood groups and secretor types in five potentially fatal diseases of Caucasian children. Acta Genet Stat Med (1965) 1.78
Gene frequencies and microdifferentiation among the Makiritare Indians. I. Eleven blood group systems and the ABH-Le secretor traits: a note on Rh gene frequency determinations. Am J Hum Genet (1970) 1.72
Polysyndactyly and Marfan's syndrome. J Med Genet (1974) 1.54
Genetic studies on the Ticuna, an enigmatic tribe of Central Amazonas. Ann Hum Genet (1980) 1.49
Studies on genetic selection in a completely ascertained caucasian population. I. Frequencies, age and sex effects, and phenotype associations for 12 blood group systems. Am J Hum Genet (1971) 1.44
Differential role of GDNF and NGF in the maintenance of two TTX-resistant sodium channels in adult DRG neurons. Brain Res Mol Brain Res (1999) 1.40
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). Cytogenet Cell Genet (1987) 1.40
Further studies on the Xavante Indians. 3. Blood groups and ABH-Lea secretor types in the Simões Lopes and São Marcos Xavantes. Am J Hum Genet (1967) 1.39
Inherited pericentric inversion of chromosome number two: a linkage study. Ann Hum Genet (1969) 1.37
Migration and genetic infrastructure of the Central American Guaymi and their affinities with other tribal groups. Am J Phys Anthropol (1982) 1.35
Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance. J Med Genet (1971) 1.32
Genetic linkage between structural loci for albumin and group specific component (Gc). Am J Hum Genet (1966) 1.28
Intra and intertribal genetic variation within a linguistic group: the Ge-speaking indians of Brazil. Am J Phys Anthropol (1977) 1.27
Plasticity of sodium channel expression in DRG neurons in the chronic constriction injury model of neuropathic pain. Pain (1999) 1.27
Cystic lymphangioma of the pancreas: CT and pathologic findings. Abdom Imaging (1998) 1.22
Expression of the intermediate filament nestin during rodent tooth development. Int J Dev Biol (1995) 1.22
Inheritance of idiopathic torsion dystonia among Jews. J Med Genet (1984) 1.20
Characterization of glial trkB receptors: differential response to injury in the central and peripheral nervous systems. Proc Natl Acad Sci U S A (1993) 1.19
Genetic differentiation in Dogrib Indians: serum protein and erythrocyte enzyme variation. Am J Phys Anthropol (1983) 1.13
GDNF mRNA in Schwann cells and DRG satellite cells after chronic sciatic nerve injury. Neuroreport (1996) 1.09
Increased levels of trkB mRNA and trkB protein-like immunoreactivity in the injured rat and cat spinal cord. Proc Natl Acad Sci U S A (1992) 1.08
Genetic studies of the Macushi and Wapishana Indians. II. Data on 12 genetic polymorphisms of the red cell and serum proteins: gene flor between the tribes. Hum Genet (1977) 1.08
Structural basis of sympathetic-sensory coupling in rat and human dorsal root ganglia following peripheral nerve injury. J Neurocytol (1999) 1.06
Chronic Gaucher's disease; clinical observations on 34 patients. Isr J Med Sci (1965) 1.05
Phase I and pharmacokinetic study of two sequences of gemcitabine and docetaxel administered weekly to patients with advanced cancer. Cancer Chemother Pharmacol (2001) 1.04
Blood groups and H-Le a salivary secretion of Brazilian Cayapo Indians. Am J Phys Anthropol (1972) 1.04
Thin ribs in neonatal myotonic dystrophy. Clin Genet (1975) 1.03
Genetic studies on hybrid populations. 3. Blood pressure in an American black community. Am J Hum Genet (1974) 1.03
Regrowth of motor axons following spinal cord lesions: distribution of laminin and collagen in the CNS scar tissue. Brain Res Bull (1993) 1.03
Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim. Am J Hum Genet (1977) 1.03
Some effects on the offspring of uncle-niece marriage in the Moroccan Jewish community in Jerusalem. Am J Hum Genet (1974) 1.02
The immunoglobulin allotypes (Gm and Km) of twelve Indian tribes of Central and South America. Am J Phys Anthropol (1978) 1.01
Teeth and tooth nerves. Prog Neurobiol (1995) 1.00
Autosomal recessive hydrotic ectodermal dysplasia. J Med Genet (1977) 0.99
Spinal axons in central nervous system scar tissue are closely related to laminin-immunoreactive astrocytes. Neuroscience (1995) 0.98
Mental retardation and congenital malformations associated with a ring chromosome 6. Clin Genet (1975) 0.97
Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. Clin Genet (1972) 0.96
The Northern and Southeastern Ojibwa: serum proteins and red cell enzyme systems. Am J Phys Anthropol (1974) 0.96
A score based on eight signs in the diagnosis of Down syndrome in the newborn. J Ment Defic Res (1980) 0.96
Reactivation of Delta-Notch signaling after injury: complementary expression patterns of ligand and receptor in dental pulp. Exp Cell Res (1999) 0.96
The St. Lawrence Island Eskimos: genetic variation and genetic distance. Am J Phys Anthropol (1981) 0.95
A lethal autosomal recessive entero-colitis of early infancy. Clin Genet (1974) 0.95
Sodium channel expression in NGF-overexpressing transgenic mice. J Neurosci Res (1999) 0.95
Adventitial cystic disease. J Foot Surg (1991) 0.95
[Course and pathogenesis of neurotrophic osteoarthropathies]. Fortschr Geb Rontgenstr Nuklearmed (1970) 0.94
A possible relationship between birth month and ABO blood type. Am J Hum Genet (1967) 0.94
Gene flow across tribal barriers and its effect among the Amazonian Içana river Indians. Am J Phys Anthropol (1986) 0.93
Unusual blood genetic characteristics among the Ayoreo Indians of Bolivia and Paraguay. Hum Biol (1978) 0.92
Relatively high prevalence of the Meckel syndrome among Jews. Isr J Med Sci (1974) 0.92
Distribution of ABO blood types among fertile and infertile women. Am J Hum Genet (1969) 0.92
Differential expression of sodium channel genes in retinal ganglion cells. Brain Res Mol Brain Res (1997) 0.92
Cellular expression of neurotrophin mRNAs during tooth development. Cell Tissue Res (1997) 0.91
Probable autosomal recessive Marfan syndrome. J Med Genet (1977) 0.91
Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis). Clin Genet (1981) 0.91
In vivo NGF deprivation reduces SNS expression and TTX-R sodium currents in IB4-negative DRG neurons. J Neurophysiol (1999) 0.90
High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel. Clin Genet (1977) 0.89
Inheritance of quantitative expression of erythrocyte glucose-6-phosphate dehydrogenase activity in the negro--a twin study. Biochem Genet (1967) 0.89
Nonrandom distribution of Gm haplotypes in East Asia. Am J Hum Genet (1973) 0.89
Tubular ectasia of the rete testis: an ultrasound diagnosis. Urology (1995) 0.89
Myelin sheath thickness and internodal length of nerve fibres in the developing feline inferior alveolar nerve. J Neurol Sci (1982) 0.89
Familial thyroglossal duct cyst. Clin Genet (1993) 0.87
Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism. J Med Genet (1969) 0.87
A pilot study of the use of placental cord blood samples in monitoring for mutational events. Mutat Res (1988) 0.87
Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus. J Med Genet (1973) 0.87
Probable autosomal dominant infantile pyloric stenosis in a large kindred. Clin Genet (1981) 0.87
Changes in nerve growth factor receptor-like immunoreactivity in the spinal cord after ventral funiculus lesion in adult cats. J Neurocytol (1992) 0.87
Familial primary vesicoureteral reflux. Clin Genet (1975) 0.87
[Aseptic necroses of the patella]. Cesk Radiol (1970) 0.87
Sympathetic nerve sprouting fails to occur in the trigeminal ganglion after peripheral nerve injury in the rat. Pain (1999) 0.86
Distribution and axonal relations of macrophages in a neuroma. Neuroscience (1993) 0.86
Congenital afibrinogenemia in 10 offspring of uncle-niece marriages. Clin Genet (1980) 0.85
Blood typing studies in American Indians: misclassification of RZ phenotypes. Am J Phys Anthropol (1970) 0.85
Distribution of P2X3 receptors in the rat trigeminal ganglion after inferior alveolar nerve injury. Neurosci Lett (1998) 0.85
Growth of ascending spinal axons in CNS scar tissue. Int J Dev Neurosci (1993) 0.85
Inferior alveolar nerve regeneration and incisor pulpal reinnervation following intramandibular neurotomy in the cat. Brain Res (1982) 0.85
AIDS-related lymphoma: an unusual cause of omental caking. AJR Am J Roentgenol (1993) 0.84
Autosomal recessive lethal infantile cytochrome C oxidase deficiency. Am J Dis Child (1991) 0.84
Neuropeptide- and tyrosine hydroxylase-immunoreactive nerve fibers in painful Morton's neuromas. Muscle Nerve (2000) 0.84
Ring chromosome 13 syndrome. Clin Genet (1975) 0.84
Pulpal axons in developing, mature, and aging feline permanent incisors. A study by electron microscopy. J Comp Neurol (1981) 0.83
Congenital contractural arachnodactyly in two double second cousins: possible homozygosity. Clin Genet (1993) 0.83
Substance P-, calcitonin gene-related peptide, growth-associated protein-43, and neurotrophin receptor-like immunoreactivity associated with unmyelinated axons in feline ventral roots and pia mater. J Comp Neurol (1994) 0.83
[Osteo-onycho dysplasia]. Z Orthop Ihre Grenzgeb (1965) 0.83
Expression of HMGB1 during tooth development. Cell Tissue Res (2006) 0.83
NGF, BDNF, NT3, NT4 and GDNF in tooth development. Eur J Oral Sci (1998) 0.82
Abnormal expression of SNS/PN3 sodium channel in cerebellar Purkinje cells following loss of myelin in the taiep rat. Neuroreport (1999) 0.82
The Northern and Southeastern Ojibawa: blood group systems and the causes of genetic divergence. Hum Biol (1975) 0.82
New studies on the Macushi Indians of northern Brazil. Ann Hum Biol (1984) 0.82
Biochemical, genetic and ultrastructural study of a family with the sea-blue histiocyte syndrome/chronic non-neuronopathic Niemann-Pick disease. Eur J Clin Invest (1978) 0.82