Standout Papers
- Thoma's Oral Pathology. (1972)
Citation Impact
Citing Papers
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
2014 Standout
Oral cavity and oropharyngeal squamous cell carcinoma—an update
2015 Standout
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
Basal cell carcinomas: attack of the hedgehog
2008 Standout
BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome
2011
Hedgehog: functions and mechanisms
2008 Standout
Clear cell neoplasms in salivary glands: Clearly a diagnostic challenge
1998
Impact of Treatment Strategy on Outcomes in Patients with Candidemia and Other Forms of Invasive Candidiasis: A Patient-Level Quantitative Review of Randomized Trials
2012 Standout
Dental agenesis in the Dariusleut Hutterite brethren: Comparisons to selected caucasoid population surveys
1990
Hedgehog signaling update
2010
Genodermatoses with profound malignant potential
1992
Anatomical, Histologic, and Genetic Characteristics of Congenital Chest Wall Deformities
2009 Standout
Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein
2001 StandoutNobel
A 52‐kb deletion in the SOST‐MEOX1 intergenic region on 17q12‐q21 is associated with van Buchem disease in the Dutch population
2002 StandoutNobel
Mineral Trioxide Aggregate: A Comprehensive Literature Review—Part III: Clinical Applications, Drawbacks, and Mechanism of Action
2010 Standout
Estimated Prevalence and Distribution of Reported Orofacial Pain in the United States
1993 Standout
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex
2000 Standout
The clinical performance of adhesives
1998 Standout
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
1996 StandoutNature
Leopard syndrome
2008
Oral Cancer and Precancerous Lesions
2002 Standout
Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction
2006
SHORT Syndrome with Partial Lipodystrophy Due to Impaired Phosphatidylinositol 3 Kinase Signaling
2013
Cleft lip and palate
2009 Standout
Preserving pulpal health of a geminated maxillary lateral incisor through multidisciplinary care
2006
Cellular, molecular, and tissue-level reactions to orthodontic force
2006 Standout
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
1995 Standout
Facial shape differences between rats selected for tame and aggressive behaviors
2017 StandoutNobel
Polymorphisms in the Sclerosteosis/van Buchem Disease Gene (SOST) Region Are Associated with Bone-Mineral Density in Elderly Whites
2004 StandoutNobel
Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis
2013 StandoutNobel
Poland’s Syndrome: Different Clinical Presentations and Surgical Reconstructions in 18 Cases
2006
Apical root resorption in orthodontically treated subjects: Analysis of edgewise and light wire mechanics
1994
Signaling by bone morphogenetic proteins directs formation of an ectodermal signaling center that regulates craniofacial development
2007
Diagnostic criteria for Walker‐Warburg syndrome
1989 Standout
Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology
1989
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
1996 Standout
Anatomical redesign for the treatment of dens invaginatus type III with open apexes
2006
Salivary gland tumours
2002 Standout
Endodontic treatment of dens invaginatus: A 5-year follow-up
2005
What We Talk About When We Talk About Fat
2014 Standout
Genetics of Peutz-Jeghers Syndrome, Carney Complex and Other Familial Lentiginoses
2000
p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development
1999 StandoutNature
Long‐Term Recurrence Rates in Previously Untreated (Primary) Basal Cell Carcinoma: Implications for Patient Follow‐Up
1989 Standout
The PI3K Pathway in Human Disease
2017 Standout
Thermal cycling procedures for laboratory testing of dental restorations
1999 Standout
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly
1996 Standout
A meta‐analysis of the prevalence of dental agenesis of permanent teeth
2004 Standout
Mutations in SUFU predispose to medulloblastoma
2002 Standout
Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13)
1989
Poland’s syndrome revisited
2002 Standout
Prevalence and Clinical Significance of Cardiovascular Abnormalities in Patients With the LEOPARD Syndrome
2007
A mouse model of Greig cephalo–polysyndactyly syndrome: the extra–toesJ mutation contains an intragenic deletion of the Gli3 gene
1993 Standout
HOLOPROSENCEPHALY AND SEPTO-OPTIC DYSPLASIA
1994
Primitive neuroectodermal tumors of the central nervous system
1983
Mouse Otx2 functions in the formation and patterning of rostral head.
1995 Standout
Familial Poland anomaly.
1982
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
Nevoid Basal-Cell Carcinoma Syndrome
1987
Children with Apert Syndrome: Developmental and Psychologic Considerations
1991
Studies of malformation syndromes of man XXXXI B: Nosologic studies in the Hanhart and the Möbius syndrome
1976
Poland syndrome in British Columbia: Incidence and reproductive experience of affected persons
1977 Standout
Signalling interactions during facial development
1998
Lipodystrophies: Genetic and Acquired Body Fat Disorders
2011
Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome
1997
Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes
2000
Sclerostin is a delayed secreted product of osteocytes that inhibits bone formation
2005 Standout
Mobius syndrome redefined
2003 Standout
Enhanced expression of the human gene N-myc consequent to amplification of DNA may contribute to malignant progression of neuroblastoma.
1984 StandoutNobel
BASAL CELL CARCINOMA IN QUEENSLAND
1981
Sclerosteosis
1983
Syndromes with cephaloceles
1982
TRANSFORMING GROWTH FACTOR-β REGULATION OF IMMUNE RESPONSES
2005 Standout
Leukoplakia, lichen planus, and other oral keratoses in 23,616 white Americans over the age of 35 years
1986
Nevoid basal cell carcinoma syndrome: Bilateral ovarian fibromas in a 3½-year-old girl
1986
Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications
2012 Standout
Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus Syndrome
1996 StandoutScience
A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly‐craniofacial anomalies syndrome
1983
Altered Neural Cell Fates and Medulloblastoma in Mouse patched Mutants
1997 StandoutScience
Dysregulation of the TSC-mTOR pathway in human disease
2004 Standout
Common oral lesions found during a mass screening examination
1986
Clinical status of dentine bonding agents
1989
Wound healing - A literature review
2016 Standout
Human N-myc gene contributes to neoplastic transformation of mammalian cells in culture
1985 StandoutNatureNobel
Genetic Analysis of the Mammalian Transforming Growth Factor-β Superfamily
2002
Works of Gorlin Rj being referenced
The multiple nevoid basal cell carcinoma syndrome revisited.
1971
Risk of recurrence in usually nongenetic malformation syndromes.
1979
The multiple nevoid basal cell carcinoma syndrome.
1970
Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis.
1971
Acinic cell tumor of the major and minor salivary glands.
1957
The Leopard (multiple lentigines) syndrome revisited.
1971
Facial variability in Apert type acrocephalosyndactyly.
1971
Thoma's Oral Pathology.
1972 Standout
Clinical identification of a human equivalent to the short ear (se) murine phenotype.
1994
Minnesota oral cancer detection 1957-1964--results.
1966
Malformation syndromes. A selected miscellany.
1975
Frontonasal dysplasia (median cleft face syndrome): comments on etiology and pathogenesis.
1971
Hereditary hearing loss associated with musculoskeletal malformations.
1980
"Newer" facial clefting syndromes.
1977