Cedric O. Carter

Cedric O. Carter's AcademicInfluence.com Rankings

Cedric O. Carter

Biology

#5259

World Rank

#7691

Historical Rank

Genetics

#468

World Rank

#539

Historical Rank

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Biology

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Cedric O. Carter'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

Mendelian Inheritance in Man (1967) (1141)
Genetics of common disorders. (1969) (316)
Inheritance of congenital pyloric stenosis. (1961) (256)
Spina Bifida and Anencephalus in Greater London (1973) (194)
Genetics of common single malformations. (1976) (186)
A family study of major central nervous system malformations in South Wales. (1968) (174)
Foetus into Man. Physical Growth from Conception to Maturity (1979) (142)
Clues to the Aetiology of Neural Tube Malformations * (1974) (138)
Genetic clinic. A follow-up. (1971) (132)
The inheritance of common congenital malformations. (1965) (120)
Chromosome translocation as a cause of familial mongolism. (1960) (117)
Inheritance of congenital pyloric stenosis. (1969) (102)
A LIFE‐TABLE FOR MONGOLS WITH THE CAUSES OF DEATH (1958) (101)
Major central nervous system malformations in South Wales. II. Pregnancy factors, seasonal variation, and social class effects. (1968) (100)
Chromosome studies in detection of parents with high risk of second child with Down's syndrome. (1961) (96)
A family study of renal agenesis (1979) (86)
RISK OF PARENTS WHO HAVE HAD ONE CHILD WITH DOWN'S SYNDROME (MONGOLISM) HAVING ANOTHER CHILD SIMILARLY AFFECTED (1961) (81)
Major central nervous system malformations in South Wales. I. Incidence, local variations and geographical factors. (1968) (81)
The carrier state in nephrogenic diabetes insipidus. (1956) (81)
A family study of bladder exstrophy. (1980) (78)
Methodology in Medical Genetics (1976) (77)
Congenital dislocation of the hip (1960) (70)
Early recognition of heterozygotes for the gene for dystrophia myotonica (1970) (69)
Genetic and environmental factors in the etiology of congenital dislocation of the hip. (1964) (66)
The genetic identity of acute infantile spinal muscular atrophy. (1973) (66)
Creatine Kinase Levels in Women who Carry Genes for Three Types of Muscular Dystrophy (1965) (65)
Children of adult survivors with spina bifida cystica. (1973) (63)
Monogenic disorders. (1977) (63)
A three generation family study of cleft lip with or without cleft palate. (1982) (58)
An ABC of medical genetics. II. Chromosomes and chromosome mutations. (1969) (56)
A family study of vesicoureteric reflux (1978) (53)
Multifactorial Genetic Disease (1970) (52)
Offspring of patients with tracheo-oesophageal fistula (1979) (51)
Spinal dysraphism: genetic relation to neural tube malformations. (1976) (49)
A FAMILY SHOWING TRANSMISSION OF A D/D RECIPROCAL TRANSLOCATION AND A CASE OF REGULAR 21-TRISOMIC DOWN'S SYNDROME. (1963) (46)
Psoriasis: prevalence, spontaneous course, and genetics (1964) (45)
Spina bifida and anencephaly: a problem in genetic–environmental interaction (1969) (44)
MATERNAL RADIATION AND DOWN'S SYNDROME (MONGOLISM) (1961) (42)
Genetic heterogeneity for dystrophia myotonica. (1972) (40)
CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES. (1965) (40)
A Family Study of Aortic Stenosis (1964) (39)
A genetic study of subacute and chronic spinal muscular atrophy in childhood A nosological analysis of 124 index patients (1978) (39)
Early-onset dystrophia myotonica. (1972) (39)
Familial hypoplastic anemia with congenital abnormalities (Fanconi's syndrome). (1952) (38)
A family study of craniosynostosis, with probable recognition of a distinct syndrome. (1982) (37)
MATERNAL STATES IN RELATION TO CONGENITAL MALFORMATIONS (1950) (35)
Recurrence risks in severe undiagnosed mental deficiency. (2008) (34)
The risk of recurrence after two children with central-nervous-system malformations. (1967) (33)
CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). II. THE FREQUENCY OF INTERCHANGE TRISOMY IN PATIENTS BORN AT A MATERNAL AGE OF LESS THAN 30 YEARS. (1965) (33)
A family study of hydrocephalus resulting from aqueduct stenosis. (1981) (32)
Two-generation pyloric stenosis. (1954) (32)
[Genetics of common malformations]. (1971) (32)
Handicap and social status of adults with spina bifida cystica (1974) (31)
Congenital Duodenal Obstruction and Mongolism (1952) (31)
Duchenne's Muscular Dystrophy and the Xg Blood Groups: a Search for Linkage (1965) (31)
Genetics and Disease (1976) (26)
Comparative Genetics in Monkeys, Apes and Man (1972) (25)
The birthplaces of parents and grandparents of a series of patients with phenylketonuria in south‐east England (1961) (25)
A new alopecia/mental retardation syndrome (1983) (23)
Aldolase Activity in the Plasma or Serum of Normal Children and Families with Muscular Dystrophy (1963) (22)
Changing patterns in the causes of death at the Hospital for Sick Children. (1956) (21)
VI—POLYGENIC INHERITANCE AND COMMON DISEASES (1969) (21)
Upper end of range of intelligence in mongolism. (1960) (20)
Use of overlapping normal distributions in genetic counselling. (1978) (20)
Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence. (1978) (19)
The Genetics of the Major Central Nervous System Malformations, Based on the South Wales Sociogenetic Investigation (1967) (19)
Recurrence risk of common congenital malformations. (1974) (18)
Human Biology: An Introduction to Human Evolution, Variation and Growth (1965) (18)
A family study of isolated cleft palate. (1982) (16)
Effect of genetic counselling on the prevalence of Huntington's chorea. (1983) (16)
THE INCIDENCE OF HEREDITARY DISEASE IN MAN (1977) (16)
A family study of the late infantile and juvenile forms of metachromatic leucodystrophy. (1966) (16)
The camptomelic syndrome in two female siblings (1980) (14)
B group short-arm deletion syndrome. (1971) (14)
Genetic Engineering: Principles and Methods, vol 2 (1981) (13)
The prevalence of respiratory disease in heterozygotes for the gene for fibrocystic disease of the pancreas. (1963) (13)
Polygenic inheritance and common diseases. (1969) (12)
Children of those treated surgically for Hirschsprung's disease. (1981) (12)
Pyloric Stenosis in Twins (1951) (12)
Recent advances in human genetics (1961) (11)
The genetics of urinary tract malformations. (1984) (11)
AMNIOCENTESES AND THE ALPHA-FETOPROTEIN SCREENING PROGRAMME (1979) (10)
Birth frequency of bilateral renal agenesis. (1981) (10)
The grandchildren of patients with pyloric stenosis (1980) (10)
Heterozygote advantage for the phenylketonuria allele. (1978) (10)
Use of creatine kinase for detecting severe X-linked muscular dystrophy carriers. (1976) (10)
Man's Haemoglobins Including the Haemoglobinopathies and their Investigation (1967) (10)
Principles of polygenic inheritance. (1977) (9)
Genetics of hyperlipoproteinaemias. (1971) (9)
Sex differences in the distribution of physical illness in children. (1978) (9)
Pyloric Stenosis in Four First Cousins (1951) (9)
COUNSELLING AND HUNTINGTON'S CHOREA (1979) (8)
Twin studies of schizophrenia (1969) (8)
The incidence of hereditary disease in man. (1977) (8)
Mothers at Work (1963) (8)
Differential Fertility by Intelligence (1966) (8)
INCIDENCE OF HEREDITARY DISEASE IN MAN (1977) (7)
NEURAL-TUBE MALFORMATIONS IN OFFSPRING OF SPINA-BIFIDA PATIENTS (1975) (7)
Care and disposal of mongolian defectives. (1954) (7)
Biosocial aspects of life in Britain. Nature and distribution of genetic abnormalities. (1973) (7)
CARRIER DETECTION IN DUCHENNE MUSCULAR DYSTROPHY (1979) (6)
Introduction to Genetics (1966) (6)
Practical Manual of Genetics (1974) (6)
Polycystic disease presenting in childhood. (1974) (6)
An Introduction to Medical Genetics, 3rd ed (1964) (5)
Pyloric stenosis: children vs sibs. (1983) (5)
A family study of protracted diarrhoea in infancy. (1981) (5)
Genetics in the aetiology of disease. (1969) (5)
Antenatal paediatrics by amniocentesis. (1970) (5)
CHROMOSOMES AND CONGENITAL MALFORMATIONS. (1963) (4)
The genetics of congenital malformations. (1968) (4)
Genetics today. (1968) (4)
Counselling in Medical Genetics 3rd edn. (1982) (4)
Genetic counselling and prenatal diagnosis. (1974) (4)
The HLA System: An Introductory Survey (1977) (4)
Anencephalus and spina bifida. (1969) (4)
GENETIC FACTORS IN CONGENITAL DISLOCATION OF THE HIP. (1963) (4)
Genetics of common congenital malformations in man. (1976) (4)
Genetics and preventive medicine. (1951) (3)
Clinical Cytogenetics and Genetics (1975) (3)
Birthweight of infants with phenylketonuria and their unaffected siblings (1978) (3)
Chromosomal Variation in Man: 3rd edn (1981) (3)
Recent advances in genetic counselling. (1979) (3)
Risks of miscarriage after amniocentesis. (1976) (3)
Equalities and inequalities in health : proceedings of the twelfth annual symposium of the Eugenics Society, London, 1975 (1976) (3)
STEROID EXCRETION OF DEHYDROEPIANDROSTERONE IN YOUNG MOTHERS OF MONGOLS. (1964) (3)
Clinical aspects of genetics, the genetics of common malformations and diseases. (1967) (3)
GENETICS OF SEVERE CONGENITAL DEAFNESS (1982) (3)
Heredity and congenital malformations. (1959) (2)
Genetical aspects of cystic fibrosis of the pancreas. (1967) (2)
The frequency of conditions due to mutant genes of large effect. (1969) (2)
The carrier state in sex-linked nephrogenic diabetes insipidus. (1957) (2)
III—THE GENES (1969) (2)
RISK OF RECURRENCE OF DOWN SYNDROME (1980) (2)
Hirschsprung's disease. (1951) (2)
The Englishman's Height (1961) (2)
Developments in human reproduction and their eugenic, ethical implications. Proceedings of the nineteenth annual symposium of the Eugenics Society, London 1982. (1983) (2)
When is familial genetic? (1982) (2)
Inheritance in Pyloric Stenosis (1961) (2)
Progress in Pediatric Radiology. Volume 4. Intrinsic Diseases of Bones. (1973) (2)
Intestinal Polyposis. (Galton Laboratory Memoirs No. 40.) (1965) (1)
Genetics . By M. W. Strickberger Pp. x+835. (MacMillan, New York, 1968) Price 80s. (1969) (1)
Immunoglobulin levels in dystrophia myotonica. (1972) (1)
VII—GENETIC COUNSELLING (1969) (1)
FRAGILITAS OSSIUM IN SWEDEN (1962) (1)
FEWER-AND BETTER ? (1975) (1)
THE MONGOL CHILD (1962) (1)
Intelligence and Fertility (1956) (1)
Public Health Aspects of Prenatal Diagnosis (1974) (1)
Treatment of Congenital Dislocation of the Hip in the Newborn (1963) (1)
Introduction to Animal Physiology and Physiological Genetics (1968) (1)
Problems of Birth Defects . By T.V.N. Persaud. Pp. 394. (MTP, Lancaster, 1976). (1978) (1)
Medical Genetics: Principles and Practice (1976) (1)
Genetics of polycystic diseases of kidney. (1970) (1)
Doctors and Overpopulation (1972) (1)
Diastrophic dwarfism. (1969) (1)
Letters to the EditorOSTEOCHONDRODYSTROPHY (1959) (1)
Genetics and incidence of cystic fibrosis. (1975) (1)
Progress in Medical Genetics (1975) (0)
Major Mental Handicap (1979) (0)
The Genetics of Gastro-intestinal Disorders (1967) (0)
ROLE OF THE CLINICAL GENETICIST (1982) (0)
Advances in Medical Genetics (1962) (0)
Book Review: Mendelian Inheritance in Man (1967) (0)
Book Review: Genetic Disorders of Man (1971) (0)
MOLECULAR GENETICS (1961) (0)
Rare Genetic Defects (1973) (0)
Human Genetics and the Public Health (1962) (0)
Book Review: The Genetics of Coeliac Disease (1981) (0)
Genes, Dreams and Realities (1972) (0)
Books and Monographs (1969) (0)
Lectures in Medical Genetics. (1967) (0)
Genetic errors of sex development. (1966) (0)
NATURAL SELECTION IN MAN (1960) (0)
Basic Genetics (1968) (0)
Heredity counseling: a symposium sponsored by the American eugenics society (1959) (0)
Surveys, Symposia, and Transactions (1969) (0)
Genetically-determined Disease and Health (1972) (0)
Symposium on Pædiatric Gynæcology [Abridged] (1966) (0)
Inherited Diatheses (1967) (0)
MONGOLISM (1954) (0)
HUMAN GENETICS (1958) (0)
THE MULTIPLICATION OF MAN (1966) (0)
Pregnancy and meningomyelocele. (1973) (0)
Genetic counselling. (1978) (0)
GARGOYLISM (1961) (0)
Book Review: Modern Trends in Human Genetics, vol 2 (1977) (0)
Book Review: Principles of Genetic Counseling (1976) (0)
The Genetic Approach to Human Disease (1979) (0)
GENETICS IN ORTHOPAEDICS (1961) (0)
Cystic Fibrosis (1966) (0)
Progress in Medical Genetics, Volume VIII. (1972) (0)
Relative contribution of chromosome abnormalities and mutant genes to genetic illhealth in man (1978) (0)
Education of the public in relation to genetic counseling. (1985) (0)
Book Review: Chromosomal Variation in Man (1981) (0)
Book Review: Genetic Engineering: Principles and Methods, Vol 2 (1981) (0)
Artificial Insemination (1945) (0)
Book Review: Oral Manifestations of Inherited Disorders (1978) (0)
Clinical Genetics: An International Journal of Genetics in Medicine (1971) (0)
syndrome . recognition of a distinct craniosynostosis , with probable A family study of (0)
GENETIC COUNSELLING AND LOOKING TO THE FUTURE. (1964) (0)
Factors determining the birth frequency of recessive conditions-a high frequency of classical phenylketonuria in Ireland. (1976) (0)
Congenital Defects (1968) (0)
Genetic counselling. (1969) (0)
Book Review: Lectures in Medical Genetics (1967) (0)
Book Review: Sex Chromosome Aneuploidy: Prospective Studies on Children (1979) (0)
Human Genetics and Medicine (1971) (0)
Book Review: Progress in Medical Genetics, Volume VIII (1972) (0)
Developments in human reproduction and their eugenic,ethical implications. Eugenic implications of new techniques. (1983) (0)
Literature on Twins (1962) (0)
Genetic Counselling (1971) (0)
Growing Points in Genetics (1969) (0)
Epidemiology of Mongolism (1971) (0)
The Genetics of Coeliac Disease (1981) (0)
Genetics and Man. (1973) (0)
Birth Defects (1964) (0)
[Methodology and effectiveness of genetic counseling]. (1980) (0)
Medical Genetics (1963) (0)
IV-MUTANT GENES OF LARGE EFFECT (1969) (0)
Proceedings of the 24th Annual Meeting of the Japan Society of Human Genetics, 1979 (1980) (0)
Modern Trends in Human Genetics, vol 2. (1977) (0)
The Clinical Pathology of Infancy (1968) (0)
Book Review: Genetic Counselling: Facts, Values, and Norms (1980) (0)
Book Review: Modern Trends in Human Genetics—1 (1971) (0)
Genetic Disorders of Man (1971) (0)
Guide to Genetics (1970) (0)
Important Topics in Genetics (1968) (0)
Genetic in orthopaedics. (1961) (0)
Book Reviews : Human Genetics: principles and methods, by Professor Ching Chun Li, PH.D. 218 pp. BLAKISTON DIVISION. MCGRAW-HILL BOOK COMPANY, INC. New York, Toronto & London, 1961. £3 6s. 0d (1962) (0)
Technical Procedures Affecting Reproduction (1975) (0)
A MONGOL CHILD WITHOUT TRISOMY G (1965) (0)
Congenital Malformations (1951) (0)
Prenatal Diagnosis (1981) (0)
Family Planning (1952) (0)
Oral Manifestations of Inherited Disorders. (1978) (0)
Effect of genetic counselling on the prevalence of Huntington's chorea (1983) (0)
Human Genetics and Its Foundations (1965) (0)
GENETIC EFFECTS OF THERMONUCLEAR EXPLOSIONS (1955) (0)
ARCHIVES OF DISEASE IN CHILDHOOD Determination of Type of Twinning (2007) (0)
International Conference on Malformations (1963) (0)
Genetic cripples. (1971) (0)

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Published Works

Cedric O. Carter's AcademicInfluence.com Rankings