Citation Impact
Citing Papers
The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome)
1994
The working brain : an introduction to neuropsychology
1973
Statistical confidence for likelihood‐based paternity inference in natural populations
1998 Standout
Reactive Oxygen Species and the Central Nervous System
1992 Standout
Pediatric multiple sclerosis
2009
Free radicals, antioxidants, and human disease: curiosity, cause, or consequence?
1994 Standout
Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
1997
The Holt-Oram syndrome.
1991
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
2004 StandoutNature
A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
2000 Standout
Relationships between gene trees and species trees.
1988 Standout
A Combined Analysis of Genomic and Primary Protein Structure Defines the Phylogenetic Relationship of New Members of the T-Box Family
1998 StandoutNobel
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
1997 Standout
TBX5 Transcription Factor Regulates Cell Proliferation during Cardiogenesis
2001
Limb malformations and the human HOX genes
2002
Mutation of HOXA13 in hand-foot-genital syndrome
1997
Multiple sclerosis
2008 Standout
Heart‐hand syndrome II. A report of Tabatznik syndrome with new findings
1990
Differential expression of VegT and Antipodean protein isoforms in Xenopus
1999 StandoutNobel
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1997 Standout
N-Acetylaspartate in the CNS: From neurodiagnostics to neurobiology
2007 Standout
Duplication of the Hoxd11 Gene Causes Alterations in the Axial and Appendicular Skeleton of the Mouse
2002 StandoutNobel
Genetic Basis for Congenital Heart Defects: Current Knowledge
2007
The neural basis of human error processing: Reinforcement learning, dopamine, and the error-related negativity.
2002 Standout
Inference of Population Splits and Mixtures from Genome-Wide Allele Frequency Data
2012 Standout
Diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria
2011 Standout
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
2003 StandoutNature
Hoxc13 mutant mice lack external hair
1998 StandoutNobel
Multiple sclerosis in children: Cerebral metabolic alterations monitored by localized proton magnetic resonance spectroscopy in vivo
1992
Increased susceptibility of HIF-1α heterozygous-null mice to cardiovascular malformations associated with maternal diabetes
2013 StandoutNobel
The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
1993 Standout
The molecular basis of hypodactyly (Hd): a deletion in Hoxa13 leads to arrest of digital arch formation
1996
Anti-inflammatory HDL becomes pro-inflammatory during the acute phase response. Loss of protective effect of HDL against LDL oxidation in aortic wall cell cocultures.
1995 Standout
Three novel TBX5 mutations in Chinese patients with Holt-Oram syndrome
2000
Multiple sclerosis in children: clinical diagnosis, therapeutic strategies, and future directions
2007
Natural History of Multiple Sclerosis with Childhood Onset
2007
Holt-Oram syndrome: a clinical genetic study.
1996
The Cell Biology of Macrophage Activation
1984 Standout
Hepatitis B Immune Serum Globulin in Prevention of Nonparenterally Transmitted Hepatitis B
1974
Blood group, serum protein and red cell enzyme groups of Amerindian populations in Colombia
1974 StandoutNobel
Adipose-Derived Stem Cells for Regenerative Medicine
2007 Standout
Hoxa11 Regulates Stromal Cell Death and Proliferation during Neonatal Uterine Development
2003 StandoutNobel
Health Consequences of Obesity in Youth: Childhood Predictors of Adult Disease
1998 Standout
Hepatitis B Virus and Sex Ratio of Offspring
1978 Science
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease
2008 Standout
Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan
2014 StandoutScienceNobel
Immunological Bases for Superior Survival of Females
1979
[1] Role of free radicals and catalytic metal ions in human disease: An overview
1990 Standout
A new ceruloplasmin variant, Cp Galveston
1970
Loss ofEph-receptorexpression correlates with loss of cell adhesion and chondrogenic capacity inHoxa13mutant limbs
2001 StandoutNobel
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
Subcellular localization of the b-cytochrome component of the human neutrophil microbicidal oxidase: translocation during activation.
1983 Standout
The possible role of elementary particle physics in cosmology
1972
Characterization, mapping, and expression of the human ceruloplasmin gene.
1986
The Course of Bone Gain and the Phases of Bone Loss
1972
Survival of Creutzfeldt-Jakob-Disease Virus in Formol-Fixed Brain Tissue
1976 StandoutNobel
Different TBX5 interactions in heart and limb defined by Holt–Oram syndrome mutations
1999
SEVERE MALARIA AND GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY: A REAPPRAISAL OF THE MALARIA/G-6-P.D. HYPOTHESIS
1979
Paralogous mouse Hox genes, Hoxa9, Hoxb9, and Hoxd9, function together to control development of the mammary gland in response to pregnancy
1999 StandoutNobel
Socioeconomic status and obesity: A review of the literature.
1989 Standout
Factors associated with graft rejection after HLA-identical marrow transplantation for aplastic anaemia
1983 StandoutNobel
GLUCOSE-6-PHOSPHATE DEHYDROGENASE AND MALARIA
1972
Exclusion of paternity: the current state of the art.
1974
Oxygen free radicals and iron in relation to biology and medicine: Some problems and concepts
1986 Standout
Genic variation within and between the three major races of man, Caucasoids, Negroids, and Mongoloids.
1974
Glucose-6-Phosphate Dehydrogenase
1985
Factors associated with graft rejection after HLA‐identical marrow transplantation for aplastic anaemia
1983 StandoutNobel
Humeral hypertrophy in response to exercise
1977 Standout
Genetic Heterogeneity
1968
Familial Hypercholesterolemia in a Large Kindred
1972 StandoutNobel
Two new ceruloplasmin variants in Negroes?Data on three populations
1970
Hoxb13is required for normal differentiation and secretory function of the ventral prostate
2003 StandoutNobel
Glucose-6-phosphate dehydrogenase deficiency
2008 Standout
Glucose-6-Phosphate Dehydrogenase Deficient Red Cells: Resistance to Infection by Malarial Parasites
1969 Science
Nutrition, Growth, Development, and Maturation: Findings From the Ten-State Nutrition Survey of 1968-1970
1975
Warfarin‐associated embryopathy in a 17‒week‐old abortus
1976
Evolution at Two Levels in Humans and Chimpanzees
1975 StandoutScience
Exponential hadronic spectrum and quark liberation
1975 StandoutNobel
Absence of Cytochrome b-245in Chronic Granulomatous Disease
1983
Secondary Sexual Characteristics and Menses in Young Girls Seen in Office Practice: A Study from the Pediatric Research in Office Settings Network
1997 Standout
Gene dosage-dependent effects of the Hoxa-13 and Hoxd-13 mutations on morphogenesis of the terminal parts of the digestive and urogenital tracts
1997
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management
2012 Standout
Deficiency of the α-Subunit of the Stimulatory G Protein and Severe Extraskeletal Ossification
2000
Creatine and Creatinine Metabolism
2000 Standout
Oxygen toxicity, oxygen radicals, transition metals and disease
1984 Standout
The Significance of the Tuberculin Skin Test in Elderly Persons
1987 Standout
Mixed cryoglobulinemia: Clinical aspects and long-term follow-up of 40 patients
1980 Standout
Gene frequencies and microdifferentiation among the Makiritare Indians. II. Seven serum protein systems.
1970
Caeruloplasmin: Physiological and Pathological Perspectives
1981
Works of John C. Gall being referenced
Possible Newly Recognized Meteorological Phenomenon called Crown Flash
1971 Nature
Skeletal Manifestations of the Holt-Oram Syndrome
1970
A SEX DIFFERENCE IN THE CARRIER STATE OF AUSTRALIA (HEPATITIS-ASSOCIATED) ANTIGEN
1971
Electrophoretic variation in human serum ceruloplasmin: A new genetic polymorphism
1967
Albumin cayemite: A Negro plasma albumin variant
1969
Holt-Oram syndrome: clinical and genetic study of a large family.
1966
Preliminary Radiogrammetric Analysis of the Bone Recovery Phase in Adolescents with Down??s Syndrome
1972
Inheritance of quantitative expression of erythrocyte glucose-6-phosphate dehydrogenase activity in the Negro?a twin study
1967
MULTIPLE SCLEROSIS IN CHILDREN
1958
Brachymesophalangia‐5 without cone‐epiphysis mid‐5 in Down's syndrome
1972
Radiographic Findings in the Hand-Foot-Uterus Syndrome (HFUS)
1970
Multiple sclerosis in children; a clinical study of 40 cases with onset in childhood.
1958
Metacarpophalangeal Pattern Profiles in the Evaluation of Skeletal Malformations
1972
The hand-foot-uterus syndrome
1970
Studies of Glucose-6-Phosphate Dehydrogenase Activity of Individual Erythrocytes: The Methemoglobin-Elution Test for Identification of Females Heterozygous for G6PD Deficiency.
1965