Citation Impact
Citing Papers
2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer: The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer
2015 Standout
Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: Developmental culling and cancer
2005 StandoutNobel
The foreign antigen binding site and T cell recognition regions of class I histocompatibility antigens
1987 StandoutNature
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A
1999
Pheochromocytoma in multiple endocrine neoplasia type 2: European study
1995
Shared genetic susceptibility of Type 1 (insulin-dependent) and Type 2 (non-insulin-dependent) diabetes mellitus: contributions of HLA and haptoglobin
1991
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
1998
The Clinical Presentation (Symptoms and Signs) of Sporadic and Familial Chromaffin Cell Tumours (Phaeochromocytomas and Paragangliomas)
2003
Genetic associations with human longevity at the APOE and ACE loci
1994 Standout
Pheochromocytomas in von Hippel-Lindau Syndrome and Multiple Endocrine Neoplasia Type 2 Display Distinct Biochemical and Clinical Phenotypes
2001
Haplotype Analysis of Hemochromatosis: Evaluation of Different Linkage-Disequilibrium Approaches and Evolution of Disease Chromosomes
1997
Structure of the human class I histocompatibility antigen, HLA-A2
1987 StandoutNature
Phaeochromocytoma
2005 Standout
Delirium as a Predictor of Mortality in Mechanically Ventilated Patients in the Intensive Care Unit
2004 Standout
Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors
1988 Standout
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex
2000 Standout
The muscular dystrophies
2002 Standout
Evidence for a Major Gene Controlling Susceptibility to Tegumentary Leishmaniasis in a Recently Exposed Bolivian Population
1997
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
On the involvement of calpains in the degradation of the tumor suppressor protein p53
1997 StandoutNobel
von Hippel-Lindau disease
2003 Standout
Graft-versus-host disease
2009 Standout
A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast
1996
Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A
2000
The CEPH Consortium Linkage Map of Human Chromosome 13
1993
Sickle-cell disease
2010 Standout
TH2 cells in systemic autoimmunity: insights from allogeneic diseases and chemically-induced autoimmunity
1991
The limb-girdle muscular dystrophies
2001
Low antibody responsiveness is found to be associated with resistance to chemical skin tumorigenesis in several lines of Biozzi mice
1999
Paradoxical roles of the immune system during cancer development
2006 Standout
Significant haemoglobinopathies: guidelines for screening and diagnosis
2010
Pheochromocytoma: The Expanding Genetic Differential Diagnosis
2003
Synaptotagmins: Why So Many?
2002 StandoutNobel
The von Hippel–Lindau protein, HIF hydroxylation, and oxygen sensing
2005 StandoutNobel
Phosphoinositides in cell regulation and membrane dynamics
2006 StandoutNature
Interest of Routine Measurement of Serum Calcitonin: Study in a Large Series of Thyroidectomized Patients
1997
Molecular basis of muscular dystrophies
2000
Protein Tyrosine Phosphatases in the Human Genome
2004 Standout
Pheochromocytoma: Update on Diagnosis, Localization, and Management
1995
HLA-DQβ gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus
1987 StandoutNature
High Serum IgG4 Concentrations in Patients with Sclerosing Pancreatitis
2001 Standout
Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A
1998
Disorders of Iron Metabolism
1999 Standout
Effect of a Novel Immunosuppressant, FK 506, on Autoimmune Glomerulonephritis in Brown Norway Rats
1999
MTM1 mutations in X-linked myotubular myopathy
2000
Mutations in Calpain 3 Associated with Limb Girdle Muscular Dystrophy: Analysis by Molecular Modeling and by Mutation in m-Calpain
2001
A new method to test genetic models in HLA associated diseases: the MASC method
1988
Leishmaniasis
1999 Standout
MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
2008 Standout
Membranous nephropathy: an IgG4-mediated disease
1998
Control of Cachectin (Tumor Necrosis Factor) Synthesis: Mechanisms of Endotoxin Resistance
1986 StandoutScienceNobel
Homozygosity for Hemochromatosis: Clinical Manifestations
1980
Bone-Marrow Transplantation for Hematologic Neoplasia in 16 Patients with Identical Twins
1974 StandoutNobel
Multivariate analysis of prognostic factors in sporadic medullary carcinoma of the thyroid: A retrospective study of 109 consecutive patients
1996
Cell Biology of the Glomerular Podocyte
2003 Standout
The mouse and human genes encoding the recognition component of the N-end rule pathway
1998 StandoutNobel
Mixed Leukocyte Stimulation of Normal Peripheral Leukocytes by Autologous Lymphoblastoid Cells
1970 Science
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991 Standout
Marrow Transplantation in Thirty "Untransfused" Patients with Severe Aplastic Anemia
1980 StandoutNobel
The Major Histocompatibility Complex — Genetics and Biology
1976
Interactive effect of Gm allotypes and HLA-B locus antigens on the human antibody response to a bacterial antigen.
1980
THE EFFECT OF AMETHOPTERIN ON THE IMMUNE RESPONSE*
1971 StandoutNobel
H‐2: Its Structure and Similarity to HL‐A
1973 StandoutNobel
Marrow grafts between canine siblings matched by serotyping and mixed leukocyte culture
1971
Hereditary Haemochromatosis
1982
LEUKÆMIC TRANSFORMATION OF ENGRAFTED HUMAN MARROW CELLS IN VIVO
1971
Mapping of the immune response genes in the major histocompatibility complex of the Rhesus monkey.
1975 StandoutNobel
Bone-Marrow Transplantation
1975 StandoutNobel
The Calpain System
2003 Standout
Bone-Marrow Transplantation
1975 Standout
Three Closely Linked Genetic Systems Relevant to Transplantation
1971
Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes
2000
Structure and physiological function of calpains
1997
Heterozygous expression of insulin-dependent diabetes mellitus (IDDM) determinants in the HLA system.
1983
Expression and Functional Characteristics of Calpain 3 Isoforms Generated through Tissue-Specific Transcriptional and Posttranscriptional Events
1999
HL‐A Antigens in Rheumatoid Arthritis
1972
Tumor Recurrence and Hypertension Persistence After Successful Pheochromocytoma Operation
1997
Conversion of Alloantigen-Specific CD8+ T Cell Anergy to CD8+ T Cell Priming through In Vivo Ligation of Glucocorticoid-Induced TNF Receptor
2006 StandoutNobel
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.
1983 StandoutNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
Genetic instability in human ovarian cancer cell lines.
1994
Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A.
1986
Allogeneic Marrow Grafting for Hematologic Malignancy Using HL-A Matched Donor-Recipient Sibling Pairs
1971
Genetic control of lipopolysaccharide induced generation of serum colony stimulating factor and proliferation of splenic granulocyte/macrophage precursor cells
1976
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs.
1995 StandoutNobel
ANKYLOSING SPONDYLITIS AND HL-A 27
1973 Standout
Genetic heterogeneity of insulin-dependent (type I) diabetes mellitus: evidence from a study of extended haplotypes.
1984
Satellite Cells and the Muscle Stem Cell Niche
2013 Standout
Genetic mapping of the hemochromatosis locus on chromosome six
1980
Cellular and Molecular Regulation of Muscle Regeneration
2004 Standout
MANAGEMENT OF HEREDITARY PHEOCHROMOCYTOMA IN VON HIPPEL-LINDAU KINDREDS WITH PARTIAL ADRENALECTOMY
1999
Prospects for the genetics of human longevity
1993
Covariance Analysis of Heart Transplant Survival Data
1977
Contribution of dendritic cells to stimulation of the murine syngeneic mixed leukocyte reaction.
1980 StandoutNobel
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
1995
Murine Ia and human DR antigens: homology of amino-terminal sequences.
1978 StandoutNobel
A BIOLOGICAL ROLE FOR THE MAJOR HISTOCOMPATIBILITY ANTIGENS
1975 StandoutNobel
Thyroid carcinoma
2003 Standout
HL-A antigens: Association with disease
1974
ANTIBODIES TO HUMAN T-LYMPHOTROPIC VIRUS TYPE-I IN PATIENTS WITH TROPICAL SPASTIC PARAPARESIS
1985 Standout
Evidence for implication of muscle-specific calpain (p94) in myofibrillar integrity.
1996
Works of N Feingold being referenced
Susceptibility to human cutaneous leishmaniasis and HLA, Gm, Km markers
1987
Phaeochromocytoma in multiple endocrine neoplasia type 2 A: survey of 100 cases
1993
Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association
1996
Genetic study of gold-salt-induced immune disorders in the rat
1995
Juvenile limb-girdle muscular dystrophy
1996
Leukocyte Groups and Acute Leukemia<xref ref-type="fn" rid="FN2">2</xref>
1968
Juvenile insulin‐dependent diabetes: a possible susceptibility gene in interaction with HLA
1981
Genetic linkage heterogeneity in myotubular myopathy.
1995
Acquired unbalanced hemoglobin chain synthesis during HIV infection.
1993
TISSUE ALLOANTIGENS PRESENT IN HUMAN LEUKOCYTES*
1966
[The sub-loci of the HL-A system. The main system of histocompatibility in man].
1969
[The second sub-locus of the HL-A system].
1969
Antibodies to HTLV‐I p24 in sera of blood donors, elderly people and patients with hemopoietic diseases in France and in French West Indies
1984
HLA and susceptibility to multiple sclerosis
1984
Polygenic regulation of antibody synthesis to sheep erythrocytes in the mouse: a genetic analysis
1976
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.
1991
Toward genetic dissection of high and low antibody responsiveness in Biozzi mice
1996
[Association phenomena in a population].
1973
CRITICAL EVALUATION OF HISTOCOMPATIBILITY IN 179 RENAL TRANSPLANTS
1971
Idiopathic Hemochromatosis: Linkage with HLA
1978
Comparison of sporadic and hereditary forms of medullary thyroid carcinoma.
1989
Mercuric chloride‐induced anti‐glomerular basement membrane antibodies in the rat Genetic control
1977
Genetic and Biological Aspects of the HL-A System of Human Histocompatibility
1970
Screening for medullary thyroid cancer in France: a national effort. French Medullary Study Group (GETC).
1989
The HL-A system sub-loci and their importance in transplantation.
1969
Genetic control of macrophage functions. I. Polygenic regulation of phagocytosis stimulation produced by Glyceryl Trioleate.
1975