Citation Impact
Citing Papers
Synthesising qualitative and quantitative evidence: A review of possible methods
2005 Standout
Epidemiology of and Diagnostic Strategies for Toxoplasmosis
2012 Standout
Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome.
1988 StandoutNobel
Use of a decision aid for prenatal testing of fetal abnormalities to improve women’s informed decision making: a cluster randomised controlled trial [ISRCTN22532458]
2008
Birth Prevalence of Congenital Heart Disease Worldwide
2011 Standout
Acquired chromosome rearrangements in human lymphocytes: effect of aging
1988
The gamma T-cell antigen receptor
1987 StandoutNobel
Molecular analysis of the antigen receptor of virus‐specific cytotoxic T cells and identification of a new Vα family
1987 StandoutNobel
The T-cell antigen receptor gamma gene: rearrangement and cell lineages
1987 StandoutNobel
The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers
1996 Standout
An evaluation of the decision‐making process regarding amniocentesis following a screen‐positive maternal serum screen result
2009
Women's Views of Pregnancy Ultrasound: A Systematic Review
2002
Applying decision analysis to facilitate informed decision making about prenatal diagnosis for Down syndrome: a randomised controlled trial
2004
Telomeres shorten during ageing of human fibroblasts
1990 StandoutNatureNobel
Genetic Testing for Prostate Cancer
2000
The Impact of Fetal Echocardiography on the Prevalence of Liveborn Congenital Heart Disease
2006
Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer
1999
Down's syndrome: The effects of prenatal diagnosis and demographic factors in a region of the eastern part of Germany
2000
Chromosome 21 and Down syndrome: from genomics to pathophysiology
2004 Standout
T-cell antigen receptor genes and T-cell recognition
1988 StandoutNature
Immunoglobulin lambda light chain orphons on human chromosome 8q11.2
1997 StandoutNobel
Listening to silence and understanding nonsense: exonic mutations that affect splicing
2002 Standout
Telomere Length, Telomere-binding Proteins, and DNA Damage Signaling
2000 StandoutNobel
Down's syndrome
2003 Standout
Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression
2002 Standout
Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study
2013 Standout
Slipped-strand mispairing: a major mechanism for DNA sequence evolution.
1987 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
Down syndrome
2020 Standout
Prenatal screening and diagnosis of congenital toxoplasmosis: a review of safety issues and psychological consequences for women who undergo screening
2007
Limited diversity of γδ antigen receptor genes of thy-1+ dendritic epidermal cells
1988 StandoutNobel
Targeted breakage of paracentromeric heterochromatin induces chromosomal instability
1998
Identification of a monoclonal antibody specific for a murine T3 polypeptide.
1987 Standout
A map of the human immunoglobulin VH locus completed by analysis of the telomeric region of chromosome 14q
1994 StandoutNobel
A Meta-Analytic Review of the Common-Sense Model of Illness Representations
2003 Standout
Communication and Uncertainty Management
2001 Standout
Leukemia and lymphoma in ataxia telangiectasia
1996
The T cell antigen receptor complex expressed on normal peripheral blood CD4-, CD8- T lymphocytes. A CD3-associated disulfide-linked gamma chain heterodimer.
1987 StandoutNobel
T-cell gamma gene is allelically but not isotypically excluded and is not required in known functional T-cell subsets.
1987 StandoutNobel
Decision aids for people facing health treatment or screening decisions
2017 Standout
Polymorphisms of a human variable heavy chain gene show linkage with constant heavy chain genes.
1984 StandoutNobel
Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q
1982 Nature
Cognitive representations of breast cancer, emotional distress and preventive health behaviour: a theoretical perspective
2000
Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7
1985 Nature
Recombination of exogenous interleukin 2 receptor gene flanked by immunoglobulin recombination signal sequences in a pre-B cell line and transgenic mice.
1991 StandoutNobel
Short telomeres and ataxia-telangiectasia mutated deficiency cooperatively increase telomere dysfunction and suppress tumorigenesis.
2003 StandoutNobel
Genomic organization of mouse J kappa recombination signal binding protein (RBP-J kappa) gene.
1992 StandoutNobel
Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus.
1983
Clonal analysis of stable chromosome rearrangements in bloom's syndrome fibroblasts
1984
Constitutive Fragile Sites and Cancer
1984 Science
Highly polymorphic DNA site D14S1 maps to the region of Burkitt lymphoma translocation and is closely linked to the heavy chain γ1 immunoglobulin locus
1982
Determination of the Number of Conserved Chromosomal Segments Between Species
2001
Structural Dynamics of Eukaryotic Chromosome Evolution
2003 StandoutScience
Immunological Memory and Protective Immunity: Understanding Their Relation
1996 StandoutScience
The Molecular Genetics of the T-Cell Antigen Receptor and T-Cell Antigen Recognition
1986
Effects of Controllability, Predictability, and Information-Seeking Style on Interest in Predictive Genetic Testing
1999
Works of Y Aurran being referenced
Cancer genetic clinics: why do women who already have cancer attend?
1998
Reasons for women's non‐uptake of amniocentesis
1994
Distribution of spontaneous chromosome breaks in man
1979
[Prenatal diagnosis: perceptions of women concerning their pregnancies].
1994
Attitudes towards cancer predictive testing and transmission of information to the family.
1996
Attitudes towards Down's syndrome: follow up of a cohort of 280 cases.
1995
Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects
1976
Impact of prenatal diagnosis by ultrasound on the prevalence of congenital anomalies at birth in southern France.
1994