Carl J. Witkop
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Why Is Carl J. Witkop Influential?
(Suggest an Edit or Addition)Carl J. Witkop's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. (1988) (615)
- Abnormal visual pathways in the brain of a human albino (1975) (186)
- Reliability of absent platelet dense bodies as a diagnostic criterion for Hermansky‐Pudlak syndrome (1987) (177)
- Albinism and Hermansky-Pudlak syndrome in Puerto Rico. (1990) (175)
- Visual system anomalies in human ocular albinos. (1978) (174)
- Hereditary defects in enamel and dentin. (1957) (171)
- Asymmetric visually evoked potentials in human albinos: evidence for visual system anomalies. (1974) (150)
- Inherited defects in tooth structure. (1971) (131)
- Manifestations of genetic diseases in the human pulp. (1971) (113)
- Studies of platelets in a variant of the Hermansky-Pudlak syndrome. (1971) (105)
- Taurodontism, an isolated trait associated with syndromes and X-chromosomal aneuploidy. (1980) (100)
- Hermansky-Pudlak syndrome. Ophthalmic findings. (1988) (99)
- Sclerosteosis: Nemogenetic and pathophysiologic analysis of an American kinship (1983) (95)
- Hereditary defects of dentin. (1975) (94)
- FOCAL EPITHELIAL HYPERPLASIA IN CENTRAL AND SOUTH AMERICAN INDIANS AND LADINOS. (1965) (81)
- Malformation syndromes. A selected miscellany. (1975) (81)
- Combined chemical and electron microscopic studies of pheomelanosomes in human red hair. (1983) (77)
- TAURODONTISM; REPORT OF A CASE. (1964) (75)
- Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis. (1967) (73)
- HYPOPLASIA AND INTRINSIC STAINING OF ENAMEL FOLLOWING TETRACYCLINE THERAPY. (1963) (73)
- Ophthalmologic, biochemical, platelet, and ultrastructural defects in the various types of oculocutaneous albinism. (1973) (72)
- Hypoplastic enamel, onycholysis, and hypohidrosis inherited as an autosomal dominant trait. A review of ectodermal dysplasia syndromes. (1975) (71)
- Oral and genetic studies of Chileans, 1960. I. Oral anomalies. (1963) (68)
- Auditory brainstem anomalies in human albinos. (1980) (66)
- An improved method for the extraction of endogenous platelet serotonin. (1976) (63)
- Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity. (1970) (63)
- Pathogenesis of pulmonary fibrosis: platelet-derived growth factor precedes structural alterations in the Hermansky-Pudlak syndrome. (1994) (59)
- The Saethre-Chotzen syndrome. (1975) (59)
- Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males. (1978) (59)
- Basal cell nevus syndrome. Combined clinical staff conference at the National Institutes of Health. (1966) (59)
- Hermansky-Pudlak syndrome in a Swiss population. (1993) (57)
- Hairbulb tyrosinase activity in oculocutaneous albinism (1976) (57)
- Autosomal recessive pigmented hypomaturation amelogenesis imperfecta. Report of a kindred. (1973) (56)
- Effects of normal and aspirin platelets on defective secondary aggregation in the Hermansky-Pudlak syndrome. A test for storage pool deficient platelets. (1972) (54)
- Four hereditary mucosal syndromes: comparative histology and exfoliative cytology of Darier-White's disease, hereditary benign intraepithelial dyskeratosis, white sponge nevus, and pachyonychia congenita. (1961) (52)
- Albinism in Nigeria with delineation of new recessive oculocutaneous type (1980) (51)
- Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolism. (1985) (51)
- Auditory System Abnormalities in Human Albinos (1982) (51)
- The influence of prostaglandin G2 on platelet ultrastructure and platelet secretion. (1977) (49)
- Dentinogenesis imperfecta in a racial isolate with multiple hereditary defects. (1956) (49)
- Taurodontism: an anomaly of teeth reflecting disruptive developmental homeostasis. (1988) (49)
- Odontodysplasia. Report of three cases with vascular nevi overlying the adjacent skin of the face. (1978) (48)
- Oral and genetic study of Chileans 1960. III. Periodontal disease and nutritional factors. (1963) (46)
- Albinism: hematologic-storage disease, susceptibility to skin cancer, and optic neuronal defects shared in all types of oculocutaneous and ocular albinism. (1979) (46)
- Prevalence of Malocclusion in Chippewa Indian Children (1968) (46)
- Hermansky-Pudlak syndrome (HPS). An epidemiologic study. (1990) (46)
- Inherited disorders of pigmentation. (1985) (45)
- Autosomal dominant hypodontia with nail dysgenesis. Report of twenty-nine cases in six families. (1975) (43)
- Sclerosteosis (1983) (43)
- Elevated urinary dolichol excretion in the Hermansky-Pudlak syndrome. Indicator of lysosomal dysfunction. (1987) (42)
- Amish albinism: a distinctive autosomal recessive phenotype. (1970) (42)
- An electron optic analysis and explanation for the etiology of dentinal dysplasia. (1972) (42)
- Tyrosinase subcellular distribution and kinetic parameters in wild type and C-locus mutant C57BL/6J mice. (1981) (41)
- Characterization of human hairbulb tyrosinase: properties of normal and albino enzyme. (1978) (40)
- Platelet aggregation independent of ADP release or prostaglandin synthesis in patients with hermansky-Pudlak syndrome. (1981) (39)
- A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism. (1991) (39)
- Agenesis of succedaneous teeth: an expression of the homozygous state of the gene for the pegged or missing maxillary lateral incisor trait. (1987) (39)
- Clinical, genetic, and histologic features of the trichoonychodental (TOD) syndrome. (1978) (38)
- Genetics and dentistry (1958) (38)
- Nucleotide profiles of normal and abnormal platelets by high-pressure liquid chromatography (1974) (38)
- The Hermansky-Pudlak syndrome: ultrastructure of bone marrow macrophages. (1973) (37)
- Sjogren-Larsson syndrome and histidinemia: hereditary biochemical diseases with defects of speech and oral functions. (1963) (37)
- A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico. (1993) (36)
- Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation. (1979) (36)
- Clinical aspects of dental anomalies. (1976) (35)
- Hermansky-Pudlak syndrome: an immunologic assessment of 15 cases. (1988) (33)
- A GENETIC STUDY OF DENTAL CARIES WITH SPECIAL REFERENCE TO PTC TASTE SENSITIVITY. (1964) (32)
- Hereditary hypophosphatemia (vitamin D-resistant rickets) presenting primary dental manifestations (1966) (32)
- Globodontia in the otodental syndrome. (1976) (32)
- Electron optic microanalysis of two gene products in enamel of females heterozygous for X-linked hypomaturation amelogenesis imperfecta. (1972) (31)
- Hermansky-Pudlak syndrome (HPS): a proposed block in glutathione peroxidase. (1973) (31)
- Optic and otic neurologic abnormalities in oculocutaneous and ocular albinism. (1982) (28)
- Heterogeneity in gingival fibromatosis. (1971) (27)
- Hereditary mucoepithelial dysplasia. Case report and review of the literature. (1989) (24)
- Detection of heterozygotes for tyrosinase-negative oculocutaneous albinism by hairbulb tyrosinase assay. (1977) (23)
- Thioredoxin reductase activity in Hermansky-Pudlak syndrome: a method for identification of putative heterozygotes. (1988) (23)
- The Coat Colors of Mice. A Model for Mammalian Gene Action and Interaction (1980) (22)
- Tyrosinase positive oculocutaneous albinism among the Zuni and the Brandywine triracial isolate: biochemical and clinical characteristics and fertility. (1972) (22)
- A Comparison Between the Widths of the Fissures of the Lower Molars of Caries-Resistant and Caries-Susceptible Albino Rats (Rattus Norvegicus) (1956) (20)
- Clinical, histologic, cytologic, and ultrastructural characteristics of the oral lesions from hereditary mucoepithelial dysplasia. A disease of gap junction and desmosome formation. (1978) (20)
- The questionable relation between cochlear pigmentation and noise-induced hearing loss. (1985) (19)
- Teeth with short, thin, dilacerated roots in patients with short stature: a dominantly inherited trait. (1982) (18)
- Medical and dental findings in the Brandywine isolate. (1966) (18)
- The Hermansky‐Pudlak Syndrome: Inclusions in Circulating Leucocytes (1973) (18)
- Molecular analyses of a tyrosinase-negative albino family. (1993) (18)
- Influence of prostaglandins E1, E2, and arachidonate on melanosomes in melanocytes and keratinocytes of anagen hair bulbs in vitro. (1975) (17)
- The role of ceroid in lung and gastrointestinal disease in Hermansky-Pudlak syndrome. (1989) (17)
- Geographic and nutritional factors in dental caries. (1962) (17)
- Hereditary benign intraepithelial dyskeratosis. II. Oral manifestations and hereditary transmission. (1960) (15)
- Inborn Errors of Metabolism with Particular Reference to Pseudohypoparathyroidism (1966) (14)
- Chromosome breaks and sister chromatid exchanges in albinos in Nigeria (1979) (14)
- Classification of albinism in man. (1971) (14)
- Synergistic effect of storage pool deficient platelets and low plasma von willebrand factor on the severity of the hemorrhagic diathesis in hermansky‐pudlak syndrome (1993) (14)
- Dental caries in relation to PTC taste sensitivity, secretor status, and salivary thiocyanate level. (1965) (14)
- Variable expression of albinism within a single kindred. (1991) (14)
- Albinism in England. (1982) (13)
- Ultrastructural study of hereditary benign intraepithelial dyskeratosis. (1977) (13)
- Electron-optic analyses of hypomineralized amelogenesis imperfecta in man. (1972) (12)
- Genetic and biochemical evidence for two forms of oculocutaneous albinism in man. (1971) (12)
- Electron optic analysis of human dentin in hypophosphatemic vitamin D-resistant rickets (report of a kindred with consanguinity). (1973) (11)
- The Hermansky-Pudlak syndrome. Evidence for a lowered 5-hydroxytryptamine content in platelets of heterozygotes. (1977) (11)
- ORAL AND GENETIC STUDY OF CHILEANS, 1960. V. FACTORS THAT INFLUENCE THE SEVERITY OF PERIODONTAL DISEASE. (1963) (10)
- Glycosaminoglycans of predentin, peritubular dentin, and dentin: a biochemical and electron microscopic study. (1976) (9)
- Alteration in the surface morphology of synchronized B-16 melanoma cell during the cell cycle. (1975) (8)
- The presence of Candida albicans in hereditary benign intraepithelial dyskeratosis. An ultrastructural observation. (1979) (8)
- GENES, CHROMOSOMES AND DENTISTRY. (1964) (8)
- Heterogeneity in Inherited Dental Traits, Gingival Fibromatosis and Amelogenesis Imperfecta (1971) (8)
- Dental genetics 1959. (1960) (8)
- Glycosaminoglycans of EDTA soluble and insoluble dentin in dentinogenesis imperfecta type I. (1976) (6)
- Depigmentations of the general and oral tissues and their genetic foundations. (1979) (6)
- Resistance to parathyroid extract in Gardner's syndrome. (1968) (6)
- Expression of melanoma neutral proteinase and collagenase potential by endocytosis. (1978) (5)
- Psychosocial factors in low-incidence genetic disease: the case of osteogenesis imperfecta. (1976) (5)
- Pulpal dysplasia. (1970) (5)
- Mutations in the melanin pigment system in man resulting in features of oculo cutaneous albinism (1972) (4)
- HEREDITARY BENIGN INTRAEPITHELIAL DYSKERATOSIS: A LINKAGE STUDY. (1965) (4)
- Fabry's disease (ceramide trihexosidase deficiency): diagnostic confirmation by analysis of dental pulp. (1972) (4)
- Genetics and dental health : proceedings of an International Symposium held at the National Institutes of Health, Bethesda, Maryland, April 4-6, 1961 (1962) (4)
- Diagnosis of late infantile neuronal "ceroid-lipofuscinosis" from histochemical and ultrastructural changes in dental pulp. (1984) (4)
- Hereditary mucoepithelial dysplasia, a disease of gap junction and desmosome formation. (1982) (4)
- Prepubertal diagnosis of Klinefelter syndrome in a patient with taurodontic teeth. (1989) (4)
- Staining and hypoplasia of enamel caused by tetracycline: case report. (1987) (4)
- Recent Advances in Dental Genetics (1963) (3)
- A study of hereditary defects occurring in a racial isolate residing in Southern Maryland; special report. (1956) (3)
- Concurrence of anorexia nervosa and yellow mutant albinism. (1980) (3)
- Human Albinism and Animal Models of Albinism (1988) (3)
- The frequency of discolored teeth showing yellow fluorescence under ultra-violet light. (1965) (2)
- A study of tri-racial isolates in Eastern United States. (1956) (2)
- [Globodontia--a new familial tooth abnormality]. (1977) (2)
- Influence of UV Light (250 nm) on Platelet Activation (1987) (1)
- Gardner's syndrome and other osteognathodermal disorders with defects in parathyroid functions. (1968) (1)
- Molbcular analysis of a tyrosinase-negative albinism (1993) (1)
- , Willys K. Silvers. Springer-Verlag, New York (1979), 379, $29.80 (1980) (0)
- ALLELISM IN HUMAN OCULOCUTANEOUS ALBINISM (2006) (0)
- Genetics and nutrition. (1967) (0)
- Contents, Vol. 187, 1993 (1993) (0)
- Genetics education and research. (1970) (0)
- Influence of Psoralen and Ultraviolet Therapy on Platelet Function and Arachidonic Acid Metabolism in Patients with Vitiligo (1987) (0)
- Disorders affecting cellular communications in oral tissues: gap junctions. (1980) (0)
- History of genetics in dentistry. (1980) (0)
- Albinism: Reply to Dr. Witkop. (1959) (0)
- Book Review:Dental Anthropology. Symposia of the Society for the Study of Human Biology, Volume V. D. R. Brothwell (1964) (0)
- Tyrosinase and Albinism. (1959) (0)
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