Citation Impact
Citing Papers
Unusual DNA Structures Associated With Germline Genetic Activity in Caenorhabditis elegans
2006 StandoutNobel
Accelerated Evolution of Conserved Noncoding Sequences in Humans
2006 StandoutScienceNobel
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
2013 StandoutScience
107th ENMC International Workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th–9th June 2002, Naarden, the Netherlands
2003
Cell type-selective secretome profiling in vivo
2020 StandoutNobel
Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity
2009
Thiazolidinediones
2004 Standout
Germline development from human pluripotent stem cells toward disease modeling of infertility
2012 StandoutNobel
Abdominal obesity and metabolic syndrome
2006 StandoutNature
Life at the edge: the nuclear envelope and human disease
2002
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 StandoutNature
The DSIF Subunits Spt4 and Spt5 Have Distinct Roles at Various Phases of Immunoglobulin Class Switch Recombination
2012 StandoutNobel
Transcription-coupled DNA repair: two decades of progress and surprises
2008
The genetics of ageing
2010 StandoutNature
The metabolic syndrome
2010 Standout
Hallmarks of aging: An expanding universe
2023 Standout
Ageing as a risk factor for neurodegenerative disease
2019 Standout
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene
2005
The muscular dystrophies
2002 Standout
Laminopathies: Multiple disorders arising from defects in nuclear architecture
2006
Regulation of nucleotide excision repair activity by transcriptional and post-transcriptional control of the XPA protein
2010 StandoutNobel
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions
2008 StandoutNature
The metabolic syndrome
2005 Standout
Nucleotide Excision Repair in Human Cells
2013 StandoutNobel
Obesity and Cardiovascular Disease: A Scientific Statement From the American Heart Association
2021 Standout
The DNA Damage Response: Making It Safe to Play with Knives
2010 Standout
Lipodystrophies: rare disorders causing metabolic syndrome
2004
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy
2008
Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
2002
Nesprin-1 and -2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity
2007
Insulin and insulin resistance:
2004 Standout
Laminopathies and the long strange trip from basic cell biology to therapy
2009
Lipoatrophy Revisited
2000
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
2009
Muscular dystrophies: genes to pathogenesis
2003
The Ig-like Structure of the C-Terminal Domain of Lamin A/C, Mutated in Muscular Dystrophies, Cardiomyopathy, and Partial Lipodystrophy
2002
Nuclear lamins: building blocks of nuclear architecture
2002
Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
2008
Mutations in the LMNA gene encoding lamin A/C
2000
Structure of the Globular Tail of Nuclear Lamin
2002
Genome-wide analysis of human global and transcription-coupled excision repair of UV damage at single-nucleotide resolution
2015 StandoutNobel
2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association/American Stroke Association
2021 Standout
Diagnosis and Management of the Metabolic Syndrome
2005 Standout
Tirzepatide Once Weekly for the Treatment of Obesity
2022 Standout
The Posttranslational Processing of Prelamin A and Disease
2009
2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines
2019 Standout
Molecular Pathology of Laminopathies
2021
A Novel Mechanism of Rapid Nuclear Neutrophil Extracellular Trap Formation in Response to Staphylococcus aureus
2010 Standout
A promiscuous biotin ligase fusion protein identifies proximal and interacting proteins in mammalian cells
2012 Standout
Management of Hyperglycemia in Type 2 Diabetes, 2018. A Consensus Report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)
2018 Standout
American Association of Clinical Endocrinologists and American College of Endocrinology Comprehensive Clinical Practice Guidelines For Medical Care of Patients with Obesity
2016
Once-Weekly Semaglutide in Adults with Overweight or Obesity
2021 Standout
Genes involved in human premature ovarian failure
2010
The Function of Nuclear Architecture: A Genetic Approach
2003
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Circadian control of XPA and excision repair of cisplatin-DNA damage by cryptochrome and HERC2 ubiquitin ligase
2010 StandoutNobel
Generation of skeletal muscle stem/progenitor cells from murine induced pluripotent stem cells
2010 StandoutNobel
2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines
2019 Standout
Works of Roberta Ricotti being referenced
The pathophysiology of abdominal adipose tissue depots in health and disease
2014
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes
2003
Mutations in theC7orf11(TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships
2006
A mutation in the X-linked Emery–Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy
2001
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B
2004
Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
2000