Ruth Wynne-Davies

Ruth Wynne-Davies's AcademicInfluence.com Rankings

Ruth Wynne-Davies

Philosophy

#10092

World Rank

#13801

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#7063

World Rank

#8686

Historical Rank

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Philosophy

Ruth Wynne-Davies's Degrees

Masters Medicine University of Oxford

Why Is Ruth Wynne-Davies Influential?

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According to Wikipedia, Ruth Wynne-Davies or Ruth Blower was a British medical doctor and scholar of orthopaedics. She researched and wrote about clubfoot and scoliosis. Life and career Wynne-Davies was born in London in 1926. She attended Oswestry High School for Girls. After finishing school, she was a land girl. She then worked as a secretary before starting her training in medicine at the Royal Free School of Medicine. She was encouraged and financially supported to do so by her uncle, Llewellyn Wynne-Davies. In 1959, she changed her name to Wynne-Davies, in his honour.

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Ruth Wynne-Davies'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

Acetabular dysplasia and familial joint laxity: two etiological factors in congenital dislocation of the hip. A review of 589 patients and their families. (1970) (373)
Familial (idiopathic) scoliosis. A family survey. (1968) (331)
A genetic survey of idiopathic scoliosis in Boston, Massachusetts. (1973) (287)
FAMILY STUDIES AND THE CAUSE OF CONGENITAL CLUB FOOT. TALIPES EQUINOVARUS, TALIPES CALCANEO-VALGUS AND METATARSUS VARUS. (1964) (276)
Genetic and environmental factors in the etiology of talipes equinovarus. (1972) (184)
Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica. (1975) (179)
Scoliosis in the elderly. (1969) (159)
Inheritance and spondylolisthesis: a radiographic family survey. (1979) (153)
GENETIC ASPECTS OF IDIOPATHIC SCOLIOSIS (1973) (146)
Congenital limb anomalies: frequency and aetiological factors: Data from the Edinburgh Register of the Newborn (1964-68) (1974) (124)
The aetiology of Perthes' disease. Genetic, epidemiological and growth factors in 310 Edinburgh and Glasgow patients. (1978) (121)
TALIPES EQUINOVARUS. A REVIEW OF EIGHTY-FOUR CASES AFTER COMPLETION OF TREATMENT. (1964) (113)
Spondylo-epiphysial dysplasia tarda with progressive arthropathy. A "new" disorder of autosomal recessive inheritance. (1982) (105)
Atlas of Skeletal Dysplasias (1986) (105)
The prevalence of skeletal dysplasias. An estimate of their minimum frequency and the number of patients requiring orthopaedic care. (1985) (101)
Infantile idiopathic scoliosis. Causative factors, particularly in the first six months of life. (1975) (100)
Achondroplasia and hypochondroplasia. Clinical variation and spinal stenosis. (1981) (84)
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia. (1996) (82)
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene. (1994) (82)
Aetiology and interrelationship of some common skeletal deformities. (Talipes equinovarus and calcaneovalgus, metatarsus varus, congenital dislocation of the hip, and infantile idiopathic scoliosis). (1982) (81)
Family studies and aetiology of club foot. (1965) (80)
A family study of neonatal and late-diagnosis congenital dislocation of the hip. (1970) (80)
The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis. (1983) (70)
Clinical examination and urinary oestrogen assays in newborn children with congenital dislocation of the hip. (1968) (64)
Homocystinuria and Marfan's syndrome. A comparison. (1972) (62)
An estimate of the population frequency of congenital malformations of the upper limb. (1982) (56)
Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. (1982) (49)
Pseudoachondroplasia: clinical diagnosis at different ages and comparison of autosomal dominant and recessive types. A review of 32 patients (26 kindreds). (1986) (49)
Two clinical variants of spondylo-epiphysial dysplasia congenita. (1982) (48)
Arthrogryposis multiplex congenita. Search for prenatal factors in 66 sporadic cases. (1976) (44)
Bilateral Failure of the Capital Femoral Epiphysis: Bilateral Perthes Disease, Multiple Epiphyseal Dysplasia, Pseudoachondroplasia, and Spondyloepiphyseal Dysplasia Congenita and Tarda (1983) (43)
Association of Perthes' disease with congenital anomalies of genitourinary tract and inguinal region. (1971) (37)
Structural and segregation analysis of the type II collagen gene (COL2A1) in some heritable chondrodysplasias. (1988) (37)
Pathogenesis of scoliosis. (1976) (36)
Familial joint laxity. (1971) (35)
Clinical and genetic patterns in osteogenesis imperfecta. (1981) (35)
Heritable Disorders in Orthopaedic Practice (1974) (30)
Five-fingered hand associated with partial or complete tibial absence and pre-axial polydactyly. A kindred of 15 affected individuals in five generations. (1983) (27)
The tricho-rhino-phalangeal syndrome. A report of 14 cases in 7 kindreds. (1986) (26)
The 1960s epidemic of arthrogryposis multiplex congenita: a survey from the United Kingdom, Australia and the United States of America. (1981) (20)
Congenital upper limb anomalies: an etiologic grouping of clinical, genetic, and epidemiologic data from 387 patients with "absence" defects, constriction bands, polydactylies, and syndactylies. (1985) (16)
Some etiologic factors in Perthes' disease. (1980) (15)
Retinitis pigmentosa, metaphyseal chondrodysplasia, and brachydactyly: an affected brother and sister. (1981) (14)
Fairbank's Atlas of general affections of the skeleton (1976) (13)
THE EPIDEMIOLOGY OF CONGENITAL DISLOCATION OF THE HIP (1972) (11)
Heritable disorders in orthopedics. (1978) (10)
Are congenital vertebral anomalies and spina bifida cystica aetiologically related? (1981) (9)
Research for genetic and environmental factors in orthopedic diseases. (1986) (9)
The frequency of mental retardation in hypochondroplasia. (1991) (8)
Genetics and Malformations of The Hand (1971) (8)
A review of genetics in orthopaedics. (1975) (7)
Two first cousins with spondyloepiphyseal dysplasia tarda (X linked recessive form), one also with poikiloderma atrophicans vasculare progressing to lymphocytic lymphoma (1982) (4)
A colour atlas of clinical genetics. (1983) (4)
A family with diaphyseal aclasis and peripheral dysostosis. (1980) (3)
Congenital vertebral anomalies and the possible aetiological relationship with spina bifida. (1981) (3)
The Dysmorphic Child: An Orthopedic Perspective (1988) (2)
Genetic and other factors in the aetiology of scoliosis (1973) (2)
Birth Defects: Original Article Series, V, 3 (1971) (2)
Birth Defects; Original Article Series, V. 4 (1971) (1)
SPONDYLO-EPIPHYSIAL DYSPLASIA TARDA WITH PROGRESSIVE ARTHROPATHY (2005) (0)
Langer-Giedion syndrome . Haematometra in the (0)
Hypermobility of Joints (1984) (0)
Genetics and congenital malformations of the hand. (1973) (0)
Skeletal dysplasias. (1987) (0)
Inherited Disorders of the Skeleton (1978) (0)
Human Achondroplasis—A Multi-disciplinary Approach (1990) (0)
Some congenital abnormalities. 2. How they are treated. (1963) (0)
Congenital vertebral anomalies : aetiology and relatio , mship to spina bifida cystica 281 (0)
The Genetics of the Skeleton (1987) (0)
Genetics and orthopaedics (1987) (0)
Hypermobility (1971) (0)
Arthrogryposis multiplex congenita : search for prenatalfactors in 66 sporadic cases 623 (0)
Some congenital abnormalities. I. Why they occur. (1963) (0)
Theinfrequency ofmalignant disease indiaphyseal aclasis andneurofibromatosi s (1983) (0)
(Talipes equinovarus andcalcaneovalgus, metatarsus varus,congenital dislocation ofthehip, andinfantile idiopathic scoliosis) (1982) (0)
Newborn ( 1964-68 ) Edinburgh Register of the factors : Data from the frequency and aetiological Congenital limb anomalies : (0)
Clinical and Genetic Patterns in Osteogenesis Irnperfecta (2006) (0)
Genetics in Orthopaedics (1974) (0)
Scoliosis, vertebral anomalies and spinal bifida. (1977) (0)
Letters to the Editor (2020) (0)
Orthopaedic Problems in Inherited Skeletal Disorders (1983) (0)
HOMOCYSTINURIA AND MARFAN9S SYNDROME (1972) (0)

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