Citation Impact
Citing Papers
The human disease network
2007 Standout
Rhizobium induces DNA damage in Caenorhabditis elegans intestinal cells
2019 StandoutNobel
PARP inhibitors: Synthetic lethality in the clinic
2017 StandoutScience
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
2013 Standout
Quantifying the mechanisms of domain gain in animal proteins
2010
The DNA-damage response in human biology and disease
2009 StandoutNature
Pancreatic cancer
2004 Standout
Treatment of Medulloblastoma with Hedgehog Pathway Inhibitor GDC-0449
2009 Standout
Myasthenia Gravis
2016 Standout
Molecular biology of squamous cell carcinoma of the head and neck
2006
Molecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndrome
2014
Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.
1994 StandoutNobel
Spatial Control of the TSC Complex Integrates Insulin and Nutrient Regulation of mTORC1 at the Lysosome
2014
The DNA double-strand break response in the nervous system
2004
PALB2 mutations in European familial pancreatic cancer families
2010
Advances in autism genetics: on the threshold of a new neurobiology
2008
Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c
2016 StandoutNobel
Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells
2009 Nature
Genetic instability syndromes with progeroid features
2007
Clonal Heterogeneity and Tumor Evolution: Past, Present, and the Future
2017 Standout
Head and neck cancer
2008 Standout
Current topics in the epidemiology of oral cavity and oropharyngeal cancers
2007
Interactions of Human Mismatch Repair Proteins MutSα and MutLα with Proteins of the ATR-Chk1 Pathway
2009 StandoutNobel
Genetically Engineered Mouse Models of Brain Cancer and the Promise of Preclinical Testing
2008
Polycystic kidney disease
2018
Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
2013
The Clinical Utility of Biomarkers in the Management of Pancreatic Adenocarcinoma
2014
FANCM and FAAP24 Function in ATR-Mediated Checkpoint Signaling Independently of the Fanconi Anemia Core Complex
2008
The molecular biology of head and neck cancer
2010 Standout
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
2013 StandoutNobel
Smad4 loss in mice causes spontaneous head and neck cancer with increased genomic instability and inflammation
2009
Inherited Predisposition to Acute Myeloid Leukemia
2014
mTOR Signaling in Growth, Metabolism, and Disease
2017 Standout
Autoimmune myasthenia gravis: emerging clinical and biological heterogeneity
2009 Standout
DNA Damage, Aging, and Cancer
2009 Standout
Multiple ATR-Chk1 Pathway Proteins Preferentially Associate with Checkpoint-Inducing DNA Substrates
2011 StandoutNobel
The Fanconi anaemia/BRCA pathway
2003
Mitotic homologous recombination maintains genomic stability and suppresses tumorigenesis
2010
Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity
2005
The emerging genetic and molecular basis of Fanconi anaemia
2001
Case–Control Study of Human Papillomavirus and Oropharyngeal Cancer
2007 Standout
Diagnosis, Genetics, and Management of Inherited Bone Marrow Failure Syndromes
2007
The Fanconi Anemia/BRCA pathway: new faces in the crowd
2005
CSF-1R inhibition alters macrophage polarization and blocks glioma progression
2013 Standout
Induced pluripotent stem cells and reprogramming: seeing the science through the hype
2009 StandoutNobel
XPD Helicase Structures and Activities: Insights into the Cancer and Aging Phenotypes from XPD Mutations
2008
Glycogen synthase kinase 3β inhibitors prevent hepatitis C virus release/assembly through perturbation of lipid metabolism
2017 StandoutNobel
Stem cell clonality and genotoxicity in hematopoietic cells: Gene activation side effects should be avoidable
2004
Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies
2011 Standout
Ocular myasthenia: diagnostic and treatment recommendations and the evidence base
2008
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
2006
Fanconi Anemia (Cross)linked to DNA Repair
2005
Characterization of the Interactome of the Human MutL Homologues MLH1, PMS1, and PMS2
2006
Chromosomal aberrations in squamous cell carcinomas of the upper aerodigestive tract: biologic insights and clinical opportunities
2005
Cell cycle, CDKs and cancer: a changing paradigm
2009 Standout
Glypican-1 identifies cancer exosomes and detects early pancreatic cancer
2015 StandoutNature
Induced pluripotent stem cell–derived hepatocytes have the functional and proliferative capabilities needed for liver regeneration in mice
2010 StandoutNobel
Identification of the FANCI Protein, a Monoubiquitinated FANCD2 Paralog Required for DNA Repair
2007
AKT/PKB Signaling: Navigating the Network
2017 Standout
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
A note on competing risks in survival data analysis
2004
In Vivo Genetic Selection of Renal Proximal Tubules
2005
The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores
2009 Standout
Single-strand break repair and genetic disease
2008
Parkinson's Disease Patient-Derived Induced Pluripotent Stem Cells Free of Viral Reprogramming Factors
2009 Standout
CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
2012
Hematopoietic Dysfunction in a Mouse Model for Fanconi Anemia Group D1
2006
Human papillomavirus-associated head and neck cancer is a distinct epidemiologic, clinical, and molecular entity
2004
Human Papillomavirus DNA and p53 Polymorphisms in Squamous Cell Carcinomas From Fanconi Anemia Patients
2003
A noninvasive genetic screening test to detect oral preneoplastic lesions
2005
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
2009 StandoutNobel
An Alternative Form of Replication Protein A Expressed in Normal Human Tissues Supports DNA Repair
2009 StandoutNobel
MuSK-antibody positive myasthenia gravis: Questions from the clinic
2008
Preservation of Fertility in Patients with Cancer
2009 Standout
Gene regulation by long non-coding RNAs and its biological functions
2020 Standout
The cancer genome
2009 StandoutNature
Pancreatic cancer
2011 Standout
Architecture of an RNA Polymerase II Transcription Pre-Initiation Complex
2013 StandoutScienceNobel
Chronic Kidney Disease Diagnosis and Management
2019 Standout
Acute Myeloid Leukemia
2015 Standout
Introduction to the Analysis of Survival Data in the Presence of Competing Risks
2016 Standout
FIG4 is a hepatitis C virus particle-bound protein implicated in virion morphogenesis and infectivity with cholesteryl ester modulation potential
2015
DOG-1 Is the Caenorhabditis elegans BRIP1/FANCJ Homologue and Functions in Interstrand Cross-Link Repair
2007
Mechanism of Eukaryotic Homologous Recombination
2008
Sexually Transmitted Diseases Treatment Guidelines, 2010
2011 Standout
How the Fanconi Anemia Pathway Guards the Genome
2009
Phosphorylation of FANCD2 on Two Novel Sites Is Required for Mitomycin C Resistance
2006
Recent Stem Cell Advances: Induced Pluripotent Stem Cells for Disease Modeling and Stem Cell–Based Regeneration
2010 StandoutNobel
Classification of Intrinsically Disordered Regions and Proteins
2014 Standout
The Origins of Medulloblastoma Subtypes
2008
ATM and ATR Substrate Analysis Reveals Extensive Protein Networks Responsive to DNA Damage
2007 StandoutScience
Transient activation of c-MYC expression is critical for efficient platelet generation from human induced pluripotent stem cells
2010 StandoutNobel
Circadian Clock, Cancer, and Chemotherapy
2014 StandoutNobel
DNA Repair Pathways in Clinical Practice: Lessons From Pediatric Cancer Susceptibility Syndromes
2006
The Ubiquitin Code
2012 Standout
mTOR: a pharmacologic target for autophagy regulation
2015 Standout
Bone Marrow Failure Syndromes
1999
2014
Molecular Mechanisms of Mammalian DNA Repair and the DNA Damage Checkpoints
2004 StandoutNobel
Works of Sat Dev Batish being referenced
Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P2 phosphatase FIG4
2011
The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans
2009
Functional assessment of TSC1 missense variants identified in individuals with tuberous sclerosis complex
2011
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
2006
High Incidence of Head and Neck Squamous Cell Carcinoma in Patients With Fanconi Anemia
2003
Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia
2003
Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool
2002
Aprataxin (APTX) gene mutations resembling multiple system atrophy
2006
Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability
2010
Anti-MuSK Myasthenia Gravis Presenting With Purely Ocular Findings
2005
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
2005
Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease
2007
Sequence variation in the Fanconi anemia gene FAA
1997
A neglected lesbian health concern: cervical neoplasia.
1996
Phenotypic Consequences of Mutations in the Fanconi Anemia FAC Gene: An International Fanconi Anemia Registry Study
1997
Genetic Heterogeneity among Fanconi Anemia Heterozygotes and Risk of Cancer
2007
Evaluation of Growth and Hormonal Status in Patients Referred to the International Fanconi Anemia Registry
2001
Somatic mosaicism in Fanconi anemia: Evidence of genotypic reversion in lymphohematopoietic stem cells
2001
A 20-year perspective on the International Fanconi Anemia Registry (IFAR)
2003
Phenotypic Consequences of Mutations in the Fanconi Anemia FAC Gene: An International Fanconi Anemia Registry Study
1997