Citation Impact
Citing Papers
Diversification, not use, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome.
1993 StandoutNobel
The human immunoglobulin VH7 gene family consists of a small, polymorphic group of six to eight gene segments dispersed throughout the VH locus
1993
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
1989 StandoutNobel
A Complete Map of the Human Immunoglobulin VH Locus
1995 StandoutNobel
To err (meiotically) is human: the genesis of human aneuploidy
2001 Standout
Cloning and sequencing of human immunoglobulin λ. gene segments
1993 StandoutNobel
Human Immunoglobulin Heavy-Chain Variable Region Genes: Organization, Polymorphism, and Expression
1991
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3
1992
Somatic insertions and deletions shape the human antibody repertoire 1 1Edited by J. Karn
1999 StandoutNobel
Structure and physical map of 64 variable segments in the 3′ 0.8–megabase region of the human immunoglobulin heavy–chain locus
1993 StandoutNobel
Comparison of the Human Germline and Rearranged VH Repertoire Reveals Complementarity between Germline Variability and Somatic Mutation
1995 StandoutNobel
A deletion hot spot in the Duchenne muscular dystrophy gene
1988
The muscular dystrophies
2002 Standout
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
HAPPY mapping of a YAC reveals alternative haplotypes in the human immunoglobulin VHlocus
1993 StandoutNobel
Antibody framework residues affecting the conformation of the hypervariable loops
1992 StandoutNobel
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology
2006 StandoutNobel
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Dystrophin: The protein product of the duchenne muscular dystrophy locus
1987 Standout
A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
1990 Standout
Oligonucleotide primers for polymerase chain reaction amplification of human immunoglobulin variable genes and design of family‐specific oligonucleotide probes
1991 StandoutNobel
Molecular cloning oflin-29, a heterochronic gene required for the differentiation of hypodermal cells and the cessation of molting inC.elegans
1991 StandoutNobel
Physical map of the 3′ region of the human immunoglobulin heavy chain locus: clustering of autoantibody-related variable segments in one haplotype.
1991 StandoutNobel
A mouse model for Down syndrome exhibits learning and behaviour deficits
1995 Standout
Immunoglobulin lambda light chain orphons on human chromosome 8q11.2
1997 StandoutNobel
New localizations of VH sequences by in situ hybridization with biotinylated probes
1990
Germline variable region gene segment derivation of human monoclonal anti-Rh(D) antibodies. Evidence for affinity maturation by somatic hypermutation and repertoire shift.
1992 StandoutNobel
Direct visualization of single copy genes on banded metaphase chromosomes by nonisotopicin situhybridization
1988
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
1990 Standout
Sequence of the human immunoglobulin diversity (D) segment locus: a systematic analysis provides no evidence for the use of DIR segments, inverted D segments, “minor” D segments or D-D recombination 1 1Edited By J. Karn
1997 StandoutNobel
The repertoire of human germline vH sequences reveals about fifty groups of VH segments with different hypervariable loops
1992 StandoutNobel
The Human Aquaporin-5 Gene
1996 StandoutNobel
Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy
1993
Physical Maps of the Mouse and Human Immunoglobulin-like Loci
1989
RsaI polymorphism of a human immunoglobulin VH5 subclass locus
1988
Molecular analysis of the armadillo locus: uniformly distributed transcripts and a protein with novel internal repeats are associated with a Drosophila segment polarity gene.
1989 StandoutNobel
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
A map of the human immunoglobulin VH locus completed by analysis of the telomeric region of chromosome 14q
1994 StandoutNobel
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
1988
A giant locus for the Duchenne and Becker muscular dystrophy gene
1987
An appraisal of the application of recombinant DNA techniques to chromosome defects
1985
Duchenne Muscular Dystrophy Involving Translocation of the dmd Gene Next to Ribosomal RNA Genes
1984 Science
Localization of human variable and constant region immunoglobulin heavy chain genes on subtelomeric band q32 of chromosome 14
1982
An Increased Percentage of Long Amyloid β Protein Secreted by Familial Amyloid β Protein Precursor (βApp 717 ) Mutants
1994 StandoutScience
The isolation of a human Ig Vλ gene from a recombinant library of chromosome 22 and estimation of its copy number
1984
Human immunoglobulin variable region genes: A new VH sequence used to detect polymorphism
1987
The physical organization of the human immunoglobulin heavy chain gene complex.
1990
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy
1985 Nature
A deletion map of the human immunoglobulin heavy chain variable region.
1991
Polymorphisms of a human variable heavy chain gene show linkage with constant heavy chain genes.
1984 StandoutNobel
A Maelll polymorphism near the dystrophin gene promoter by restriction of amplified DNA
1990 StandoutNobel
PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs
1985
A truncated immunoglobulin epsilon pseudogene is found in gorilla and man but not in chimpanzee.
1985 StandoutNobel
Cellular Oncogenes (c-erb-A and c-erb-B) Located on Different Chicken Chromosomes Can Be Transduced into the Same Retroviral Genome
1984 StandoutNobel
Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.
1985
Idiopathic Pulmonary Fibrosis: Prevailing and Evolving Hypotheses about Its Pathogenesis and Implications for Therapy
2001 Standout
Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia
1985 StandoutScienceNobel
Chromosome maps of man and mouse II
1984
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy.
1994 Standout
Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization.
1983
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1987 Standout
Differential activity of maternally and paternally derived chromosome regions in mice
1985 StandoutNature
The human aquaporin-CHIP gene. Structure, organization, and chromosomal localization
1993 StandoutNobel
Analysis of nucleolar organizing regions in parents of trisomic spontaneous abortions
1987
The neurobiologie consequences of down syndrome
1986
Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus.
1983
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
1990 StandoutScience
Genetic Studies in Familial Fibrosing Alveolitis
1986
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.
1985
Somatic Cell Genetics and Gene Families
1983 Science
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy
1987
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
The Complete Nucleotide Sequence of the Human Immunoglobulin Heavy Chain Variable Region Locus
1998 StandoutNobel
Strategies for multilocus linkage analysis in humans.
1984 Standout
Multiple gene deletions within the human immunoglobulin heavy-chain cluster.
1984
DNA restriction fragments associated with α1-antitrypsin indicate a single origin for deficiency allele PI Z
1985 Nature
Isolation and characterization of rat and human glyceraldehyde-3-phosphate dehydrogenase cDNAs: genomic complexity and molecular evolution of the gene
1985 Standout
A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome
1986
Nucleolar organizer region variants as a risk factor for Down syndrome.
1985
Dispersed chromosomal localization of the proto-oncogenes transduced into the genome of Mill Hill 2 or E26 leukemia virus
1986 StandoutNobel
Human neoplastic B cells express more than two isotypes of immunoglobulins without deletion of heavy-chain constant-region genes.
1987 StandoutNobel
Results of a Triple Blind Clinical Study of Myoblast Transplantations without Immunosuppressive Treatment in Young Boys with Duchenne Muscular Dystrophy
1993
Works of V. D. Marković being referenced
Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q
1982 Nature
Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.
1980
Evidence for the inheritance of silver-stained nucleolus organizer regions
1978
Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome
1984