Citation Impact
Citing Papers
Vitamin D and Myocardial Infarction
1974
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome
2011
Molecular Basis of Oculocutaneous Albinism.
1994
The FGF family: biology, pathophysiology and therapy
2009 Standout
High Prevalence of Vitamin D Inadequacy and Implications for Health
2006 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
The Utility of DNA Typing in Forensic Work
1991 StandoutScience
Bcl-2 functions in an antioxidant pathway to prevent apoptosis
1993 Standout
SHORT Syndrome with Partial Lipodystrophy Due to Impaired Phosphatidylinositol 3 Kinase Signaling
2013
Separation of pigmented and albino melanocytes and the concomitant evaluation of endogenous peroxide content using flow cytometry
1989
Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair
1993 Standout
Dentin dysplasia type I: report of atypical cases in the permanent and mixed dentitions
2004
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
What We Talk About When We Talk About Fat
2014 Standout
The PI3K Pathway in Human Disease
2017 Standout
Biology of hypopigmentation
1988
Multicopper Oxidases and Oxygenases
1996 Standout
Actinomyces and Related Organisms in Human Infections
2015 Standout
Radiologic manifestations of Cowden disease
1980
Cowden's disease (multiple hamartoma and neoplasia syndrome)
1983 Standout
A Toll-Like Receptor 2-Responsive Lipid Effector Pathway Protects Mammals against Skin Infections with Gram-Positive Bacteria
2005 StandoutNobel
Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation.
1979
W/kit gene required for interstitial cells of Cajal and for intestinal pacemaker activity
1995 StandoutNature
Lipodystrophies: Genetic and Acquired Body Fat Disorders
2011
Sclerostin is a delayed secreted product of osteocytes that inhibits bone formation
2005 Standout
Gene admixture in human populations: Models and predictions
1986
Sclerosteosis
1983
A unifying aetiological explanation for anomalies of human tooth number and size
1984 Standout
Genetic Transmission of Tumoral Calcinosis: Autosomal Dominant with Variable Clinical Expressivity*
1985
Hypertrichosis with hereditary gingival hyperplasia
1974
Works of Witkop Cj being referenced
Hereditary benign intraepithelial dyskeratosis. II. Oral manifestations and hereditary transmission.
1960
Hereditary defects of dentin.
1975
Classification of albinism in man.
1971
Depigmentations of the general and oral tissues and their genetic foundations.
1979
Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.
1971
Heterogeneity in gingival fibromatosis.
1971
Malformation syndromes. A selected miscellany.
1975
Medical and dental findings in the Brandywine isolate.
1966
Genetics and nutrition.
1967