Citation Impact
Citing Papers
A Sulfilimine Bond Identified in Collagen IV
2009 StandoutScienceNobel
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17
1989
Stem cells, cancer, and cancer stem cells
2001 StandoutNature
At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma
1989
Defects in a cell cycle checkpoint may be responsible for the genomic instability of cancer cells
1992 StandoutNobel
Genetic analysis of NF1: Identification of close flanking markers on chromosome 17
1987
An alternative pathway for yeast telomere maintenance rescues est1− senescence
1993 StandoutNobel
The human Y chromosome shows a low level of DNA polymorphism
1990
ALLELE LOSS ON SHORT ARM OF CHROMOSOME 17 IN BREAST CANCERS
1988
Patterns of polymorphism and linkage disequilibrium for cystic fibrosis
1987
The neurofibromatosis type 1 gene encodes a protein related to GAP
1990 Standout
Molecular and genetic analysis of cystic fibrosis*1
1988
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
1991 Standout
A long-range restriction map encompassing the cystic fibrosis locus and its closely linked genetic markers
1988
Regional mapping panel for human chromosome 17: Application to neurofibromatosis type 1
1987
When Checkpoints Fail
1997 StandoutNobel
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
McrA and McrB restriction phenotypes of someE.colistrains and implications for gene cloning
1988
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations
1990
Tumor suppressor genes
1991 Standout
CLINIC EXPERIENCE OF PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY USE OF LINKED DNA PROBES
1987
A genetic map of human chromosome 17p
1990
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
1989 StandoutNobel
Molecular genetic analysis of tumors in von recklinghausen neurofibromatosis: Loss of heterozygosity for chromosome 17
1989
SNAP receptors implicated in vesicle targeting and fusion
1993 StandoutNatureNobel
Evidence implicating at least two genes on chromosome 17p in breast carcinogenesis
1990
A genetic linkage map of the human genome
1987
Salmonella typhi uses CFTR to enter intestinal epithelial cells
1998 StandoutNatureNobel
Altered cell cycle arrest and gene amplification potential accompany loss of wild-type p53
1992
A search for restriction fragment length polymorphism on the human Y chromosome
1989
Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping
1987 Nature
Male–female differences in fertility and blood pressure in ACE-deficient mice
1995 StandoutNatureNobel
Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes
1994
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia
1996
Spoken Language Development in Children Following Cochlear Implantation
2010 Standout
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
1990 Standout
Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen
2003
Twenty loci form a continuous linkage map of markers for human chromosome 2
1989
Developmentally programmed healing of chromosomes by telomerase in tetrahymena
1991 StandoutNobel
Genetic Alterations during Colorectal-Tumor Development
1988 Standout
The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins
1990
A mapped set of DNA markers for human chromosome 15
1988
The C. elegans gene lin-44, which controls the polarity of certain asymmetric cell divisions, encodes a Wnt protein and acts cell nonautonomously
1995 StandoutNobel
A 12 megabase restriction map at the cystic fibrosis locus
1989
Mammalian collagen IV
2008
Localization of a locus for Charcot-Marie-Tooth neuropathy type la (CMT1A) to chromosome 17
1990
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension
1992
Cellubrevin is a ubiquitous tetanus-toxin substrate homologous to a putative synaptic vesicle fusion protein
1993 StandoutNatureNobel
Cyclin A and the retinoblastoma gene product complex with a common transcription factor
1991 StandoutNatureNobel
Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
1993 Standout
Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis
1988
The Cystic Fibrosis Transmembrane Conductance Regulator Gene
1995
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
1989
An Animal Model for Cystic Fibrosis Made by Gene Targeting
1992 StandoutScienceNobel
Linkage disequilibrium, cystic fibrosis, and genetic counseling.
1989
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.
1990
Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene.
1988
Human Breast Cancer: Correlation of Relapse and Survival with Amplification of the HER-2/neuOncogene
1987 StandoutScience
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria
1987
Recombinations between IRP and cystic fibrosis.
1988
Gene losses in human tumours
1988 Nature
Studies of cystic fibrosis in Hutterite families by using linked DNA probes.
1987
[14] Host strains that alleviate underrepresentation of specific sequences: Overview
1987
Nanoscale distribution of mitochondrial import receptor Tom20 is adjusted to cellular conditions and exhibits an inner-cellular gradient
2011 StandoutNobel
Synaptobrevin/vesicle-associated membrane protein (VAMP) of Aplysia californica: structure and proteolysis by tetanus toxin and botulinal neurotoxins type D and F.
1994 StandoutNobel
The application of molecular genetics to detection of craniofacial abnormality
1988
Further linkage data on cystic fibrosis: the Utah Study.
1986
Host/vector interactions which affect the viability of recombinant phage lambda clones
1986
Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population.
1996 StandoutNobel
THE MOLECULAR GENETICS OF CELLULAR ONCOGENES
1984
Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17.
1990
Isolation of the proto-oncogene c-myb from D. melanogaster
1985 StandoutNobel
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.
1990
FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WITH LINKED DNA PROBES
1986
Progress towards identifying the neurofibromatosis (NF1) gene
1989
Efficient computations in multilocus linkage analysis.
1988
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.
1989
Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).
1989
Cell Cycle Control and Cancer
1994 StandoutScienceNobel
Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7.
1987
Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families.
1988
Preparation of high titer lambda phage lysates
1987
Mitotic recombination of chromosome 17 in astrocytomas.
1989
Two NF1 Translocations Map Within a 600-Kilobase Segment of 17q11.2
1989 Science
Requirement for a GTPase-Activating Protein in Vesicle Budding from the Endoplasmic Reticulum
1993 StandoutScienceNobel
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).
1990
Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.
1990
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands
1987 Nature
Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism.
1986
Cases of neurofibromatosis with rearrangements of chromosome 17 involving band 17q11.2
1987
Sequence variation of the human Y chromosome
1995 StandoutNatureNobel
Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type I.
1989
Identification of a human transcription unit affected by the variant chromosomal translocations 2;8 and 8;22 of Burkitt lymphoma.
1989 StandoutNobel
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Paralogous mouse Hox genes, Hoxa9, Hoxb9, and Hoxd9, function together to control development of the mammary gland in response to pregnancy
1999 StandoutNobel
Cell-type-specific and hypoxia-inducible expression of the human erythropoietin gene in transgenic mice.
1991 StandoutNobel
Translocation of Proteins into Mitochondria
2007
A lymphocyte-specific protein-tyrosine kinase gene is rearranged and overexpressed in the murine T cell lymphoma LSTRA
1985 StandoutNobel
Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition.
1985
Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21
1990 StandoutScience
Telomeres and Their Synthesis
1990 StandoutScienceNobel
Linkage of DNA markers to cystic fibrosis in 26 families.
1986
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study.
1986
Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene.
1989
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
1990 StandoutScience
Clonal Analysis of Human Colorectal Tumors
1987 Science
DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis.
1989
The Molecular Genetics of Cancer
1987 StandoutScienceNobel
Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping
1987 Science
Precise localization of NF1 to 17q11.2 by balanced translocation.
1989
Reverse genetics and human disease
1986
A closely linked genetic marker for cystic fibrosis
1985 Nature
A strategy of exon shuffling for making large peptide repertoires displayed on filamentous bacteriophage.
1996 StandoutNobel
Chlorophyll fluorescence—a practical guide
2000 Standout
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.
1990
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.
1989
Cloning human telomeric DNA fragments into Saccharomyces cerevisiae using a yeast-artificial-chromosome vector.
1989
A cellular gene encodes scrapie PrP 27-30 protein
1985 StandoutNobel
Derivation of Clones Close to met by Preparative Field Inversion Gel Electrophoresis
1987 Science
Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism
1985 Nature
Genetic analysis of cystic fibrosis using linked DNA markers.
1986
Construction of a General Human Chromosome Jumping Library, with Application to Cystic Fibrosis
1987 Science
Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.
1989
Physical Mapping of a Translocation Breakpoint in Neurofibromatosis
1989 Science
Polycythemia in transgenic mice expressing the human erythropoietin gene.
1989 StandoutNobel
Structure and function of telomeres
1991 StandoutNatureNobel
Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.
1988
Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysis
1987
Palaeoproteomic evidence identifies archaic hominins associated with the Châtelperronian at the Grotte du Renne
2016 StandoutNobel
Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2.
1990 StandoutNobel
Evolution of maize inferred from sequence diversity of an Adh2 gene segment from archaeological specimens.
1993 StandoutNobel
Genetic homogeneity of cystic fibrosis
1986
Oncogenes and human breast cancer.
1989
A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.
1989
Mechanisms of p53 loss in human sarcomas.
1990
Human N-myc gene contributes to neoplastic transformation of mammalian cells in culture
1985 StandoutNatureNobel
Cleft palate in mice with a targeted mutation in the γ-aminobutyric acid-producing enzyme glutamic acid decarboxylase 67
1997 StandoutNobel
Works of David Barker being referenced
Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2
1991
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17
1989
Predicting behavior problems in deaf and hearing children: The influences of language, attention, and parent–child communication
2009
The xanthophyll cycle and energy dissipation in differently oriented faces of the cactus Opuntia macrorhiza
1997
A mapped set of DNA markers for human chromosome 17
1988
Tightly linked markers for the neurofibromatosis type 1 gene
1987
A test of the role of two oncogenes in inherited predisposition to colon cancer.
1983
Factors which equalize the representation of genome segments in recombinant libraries
1986
Genetic analysis of eight loci tightly linked to neurofibromatosis 1.
1989
Rapid changes in xanthophyll cycle‐dependent energy dissipation and photosystem II efficiency in two vines, Stephania japonica and Smilax australis, growing in the understory of an open Eucalyptus forest
1999
Linkage of cystic fibrosis to the proα 2(I) collagen gene, COL1A2, on chromosome 7
1986
High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing.
1998
A locus on chromosome 11p with multiple restriction site polymorphisms.
1984
Genetic linkage map of human chromosome 7 with 63 DNA markers.
1987
Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17
1987 Science
DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22.
1984
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
1995
Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA Marker
1985 Science
Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.
1982