Citation Impact
Citing Papers
Tobacco use and cessation for cancer survivors: An overview for clinicians
2014
Circulating microRNAs as stable blood-based markers for cancer detection
2008 Standout
Chromosome Abnormalities and Genetic Counseling
2011
Complete Genetic Correction of iPS Cells From Duchenne Muscular Dystrophy
2009 StandoutNobel
Down-Regulation of Na+/K+ATPase Activity by Human Parvovirus B19 Capsid Protein VP1
2013 Standout
The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP
1987
MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations
1987 Standout
Infection by Parvovirus B 19 During Pregnancy
1997
The development of human linkage analysis
1986
What threat is human parvovirus B19 to the fetus? A review
1989
DNA Sequencing versus Standard Prenatal Aneuploidy Screening
2014 Standout
A Chromosomal Deletion Map of Human Malformations
1998
Maternal Immune Activation Alters Fetal Brain Development through Interleukin-6
2007 Standout
Label-retaining cells reside in the bulge area of pilosebaceous unit: Implications for follicular stem cells, hair cycle, and skin carcinogenesis
1990 Standout
Bootstrapping in human genetic linkage
1994
Corneal Reconstruction with Tissue-Engineered Cell Sheets Composed of Autologous Oral Mucosal Epithelium
2004 Standout
SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials
2013 Standout
Long-term restoration of damaged corneal surfaces with autologous cultivated corneal epithelium
1997 Standout
Blinding in Randomized Clinical Trials: Imposed Impartiality
2011
Existence of slow-cycling limbal epithelial basal cells that can be preferentially stimulated to proliferate: Implications on epithelial stem cells
1989 Standout
Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome
2001
An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome
1989
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies
1988
Trends in the use of prenatal diagnosis in New York State and the impact of biochemical screening on the detection of Down syndrome: 1984–1993
1997
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
Stem cells find their niche
2001 StandoutNature
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
1993 Standout
REPuter: the manifold applications of repeat analysis on a genomic scale
2001 Standout
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Multi-Ethnic Study of Atherosclerosis: Objectives and Design
2002 Standout
Dystrophin: The protein product of the duchenne muscular dystrophy locus
1987 Standout
Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localization
1987
Clinical and histopathological features of parvovirus B19 infection in the human fetus
1992
A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
1990 Standout
Eye and Kidney
2003
Molecular cloning oflin-29, a heterochronic gene required for the differentiation of hypodermal cells and the cessation of molting inC.elegans
1991 StandoutNobel
Hematopoietic Reconstitution in a Patient with Fanconi's Anemia by Means of Umbilical-Cord Blood from an HLA-Identical Sibling
1989 Standout
Detection of genetic heterogeneity for complex quantitative phenotypes
1992
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
1994 Standout
Tuberous sclerosis
2008 Standout
TOXOPLASMOSIS AND PARVOVIRUS B19
1997
Management and outcomes of pregnancies complicated by human B19 parvovirus infection: A prospective study
1990
Hereditary Colorectal Cancer
2003 Standout
FIRST-TRIMESTER BIOCHEMICAL SCREENING FOR DOWN SYNDROME
2001
Molecular, cellular and clinical aspects of Parvovirus B19 infection
1994
Telomeric repeat from T. thermophila cross hybridizes with human telomeres
1988 StandoutNatureNobel
Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis
1987
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
1990 Standout
Subventricular Zone Astrocytes Are Neural Stem Cells in the Adult Mammalian Brain
1999 Standout
Capturing and profiling adult hair follicle stem cells
2004 Standout
Antenatal diagnosis and palliative treatment of non‐immune hydrops fetalis secondary to fetal parvovirus B19 infection
1989
Single amino-acid changes in HIV envelope affect viral tropism and receptor binding
1989 StandoutNatureNobel
Down's syndrome
2003 Standout
Controlling Cell Behavior Electrically: Current Views and Future Potential
2005 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
Parvovirus B19 Infection in Pregnancy
2014
Parvovirus B19
2004 Standout
Circulating nucleic acids in plasma/serum
2007
Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis
2003 Standout
Production of monoclonal antibodies to group A erythrocytes, HLA and other human cell surface antigens-new tools for genetic analysis
1978 Standout
Mouse and hamster mutants as models for Waardenburg syndromes in humans.
1990
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
1980 Standout
Cell Biology of the Glomerular Podocyte
2003 Standout
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
THE EVOLUTION OF MULTIGENE FAMILIES: Human Haptoglobin Genes
1986 StandoutNobel
The human T-cell receptor α-chain gene maps to chromosome 14
1985 StandoutNatureNobel
Placental and Fetal Membrane Nephrin and Neph1 Gene Expression: Response to Inflammation
2005
Common Region on Chromosome 14 in T-Cell Leukemia and Lymphoma
1984 Science
In vitro growth and differentiation of rabbit bulbar, fornix, and palpebral conjunctival epithelia. Implications on conjunctival epithelial transdifferentiation and stem cells.
1993
Haptoglobin: The Evolutionary Product of Duplication, Unequal Crossing Over, and Point Mutation
1982
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1987 Standout
Cancer treatment and survivorship statistics, 2016
2016 Standout
Genetic Dissection of Complex Traits
1994 StandoutScience
The Status of the Gene Map of the Human Chromosomes
1977 Science
Cancer treatment and survivorship statistics, 2019
2019 Standout
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
1990 StandoutScience
p63 identifies keratinocyte stem cells
2001 Standout
Distinct variants of erythrocyte protein 4.1 inherited in linkage with elliptocytosis and Rh type in three white families
1988 StandoutNobel
First‐trimester contingent screening for trisomy 21 by biomarkers and maternal blood cell‐free DNA testing
2013
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Cytogenetic studies on patients with chronic T cell leukemia/lymphoma
1984
EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9
1987
Foetal intracardiac transfusion for the treatment of severe anaemia due to human parvovirus B‐19 infection
1998
Erythrocyte P Antigen: Cellular Receptor for B19 Parvovirus
1993 StandoutScience
A polymorphic DNA marker genetically linked to Huntington's disease
1983 StandoutNature
Mapping the Human Genome, Cloned Genes, DNA Polymorphisms, and Inherited Disease
1982
Works of D.A. Aitken being referenced
Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers
1987
First Trimester Biochemical Screening for Trisomy 21: The Role of Free Beta hCG, Alpha Fetoprotein and Pregnancy Associated Plasma Protein A
1994
Reliability of self reported smoking status by pregnant women for estimating smoking prevalence: a retrospective, cross sectional study
2009
First‐trimester combined ultrasound and biochemical screening for Down syndrome in routine clinical practice
2004
Prenatal screening for chromosome abnormalities using maternal serum chorionic gonadotrophin, alpha‐fetoprotein, and age
1991
BIOCHEMICAL MARKERS OF TRISOMY 21 IN AMNIOTIC FLUID
1997
Maternal serum alpha-fetoprotein levels in congenital nephrosis
1997
Regional assignment of nucleoside phosphorylase by exclusion to 14q13
1978
An ultrastructural study of rabbit ocular surface transdifferentiation.
1988
Cross-trimester repeated measures testing for Down’s syndrome screening: an assessment
2010
Gene dosage evidence for the regional assignment of the <i>GOTs </i>structural gene locus to 10q24→10q25
1978
Two years' prospective experience using fluorescencein situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies
1999
Gene mapping by exclusion: the current status
1976
Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.
1989
Tuberous sclerosis: analysis of linkage to red cell and plasma protein markers
1987
Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)
1987
The contribution of chromosome aberrations to the precision of human gene mapping
1982
MATERNAL SERUM α-FETOPROTEIN—A MARKER OF FETAL APLASTIC CRISIS DURING INTRAUTERINE HUMAN PARVOVIRUS INFECTION
1987
Heterozygosity at the α-haptoglobin locus associated with a deletion, 16q22→16qter
1978
Microvillar enzyme analysis in amniotic fluid and the prenatal diagnosis of cystic fibrosis
1985
Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34
1976