Citation Impact
Citing Papers
Co-incidence of RCC-susceptibility polymorphisms with HIF cis-acting sequences supports a pathway tuning model of cancer
2019 StandoutNobel
Depression
2018 Standout
HPA axis in major depression: cortisol, clinical symptomatology and genetic variation predict cognition
2016
Finishing the euchromatic sequence of the human genome
2004 StandoutNature
To err (meiotically) is human: the genesis of human aneuploidy
2001 Standout
The amyloid cascade hypothesis for Alzheimer's disease: an appraisal for the development of therapeutics
2011 Standout
The Tuberous Sclerosis Complex
2006 Standout
Changes of Intestinal Functions in Liver Cirrhosis
2016 Standout
Variant Alzheimer Disease With Spastic paraparesis: Neuropathological phenotype
2001
Chronic inflammation in the etiology of disease across the life span
2019 Standout
Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis
1998 StandoutNobel
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease
1992
The Many Roles of BAF (mSWI/SNF) and PBAF Complexes in Cancer
2016
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3
1992
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
1995 Standout
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1996 StandoutNature
Acute-on chronic liver failure
2012
Patterns of Meiotic Recombination on the Long Arm of Human Chromosome 21
2000
Integrative neurobiology of metabolic diseases, neuroinflammation, and neurodegeneration
2015
Mechanisms of decompensation and organ failure in cirrhosis: From peripheral arterial vasodilation to systemic inflammation hypothesis
2015
Presenilin-1 Knockin Mice Reveal Loss-of-Function Mechanism for Familial Alzheimer’s Disease
2015
Cloning of a Human RNA Editing Deaminase (ADARB1) of Glutamate Receptors That Maps to Chromosome 21q22.3
1997
Microglia and CNS Interleukin-1: Beyond Immunological Concepts
2018
Clinical, Pathological, and Biochemical Spectrum of Alzheimer Disease Associated With PS-1 Mutations
2004
The 1993–94 Généthon human genetic linkage map
1994 Standout
Dialkyl phosphates in amniotic fluid as a biomarker of fetal exposure to organophosphates in Crete, Greece; association with fetal growth
2014
Lessons from Hereditary Colorectal Cancer
1996 Standout
DNA methylation: roles in mammalian development
2013 Standout
Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map
1994
The yeast chromatin remodeler Rsc1-RSC complex is required for transcriptional activation of autophagy-related genes and inhibition of the TORC1 pathway in response to nitrogen starvation
2015 StandoutNobel
From Krebs to clinic: glutamine metabolism to cancer therapy
2016 Standout
Preventing or reducing late side effects of radiation therapy: radiobiology meets molecular pathology
2006 Standout
Exposure to pesticides and the associated human health effects
2016 Standout
Histone H1 Variants Are Differentially Expressed and Incorporated into Chromatin during Differentiation and Reprogramming to Pluripotency
2011
Acute kidney injury
2019 Standout
Persistent behavioral alterations in rats neonatally exposed to low doses of the organophosphate pesticide, parathion
2008
The clinical syndrome of Alzheimer's disease: aspects particularly relevant to clinical trials
2004
Portal hypertensive bleeding in cirrhosis
2016 Standout
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
1997 Standout
Depression as a Microglial Disease
2015
A mouse model for Down syndrome exhibits learning and behaviour deficits
1995 Standout
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1997 Standout
Chromosome 21 and Down syndrome: from genomics to pathophysiology
2004 Standout
Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy
2013 Standout
Tuberous sclerosis
2008 Standout
Gut-liver axis in liver cirrhosis: How to manage leaky gut and endotoxemia
2015
The interaction of HIV with dendritic cells: outcomes and pathways
2007 StandoutNobel
Genomic instability occurs in colorectal carcinomas but not in adenomas
1993
Histone H1 Depletion Impairs Embryonic Stem Cell Differentiation
2012
Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans
1998
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
1995 Standout
Epidemiology, Pathophysiology, and Management of Hepatorenal Syndrome
2018
Acute-on-Chronic Liver Failure Is a Distinct Syndrome That Develops in Patients With Acute Decompensation of Cirrhosis
2013 Standout
Current issues in organophosphate toxicology
2005
Kidney biomarkers in cirrhosis
2016
p63 is a p53 homologue required for limb and epidermal morphogenesis
1999 StandoutNature
A method for constructing radiation hybrid maps of whole genomes
1994
Chromatin remodeller SMARCA4 recruits topoisomerase 1 and suppresses transcription-associated genomic instability
2016 StandoutNobel
Neurobehavioural effects of developmental toxicity
2014 Standout
A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function
1997 StandoutNature
Report of the fourth international workshop on human chromosome 21
1993
Molecular biomarkers of depression
2016
10 Years ofGenomics,Chromosome 21, and Down Syndrome
1998
Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q
1993
European Gene Mapping Project(EUROGEM): Genetic Maps basedon the CEPH reference families
1994 Nobel
Inflammation in obesity, diabetes, and related disorders
2022 Standout
Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life
2005
The amyloid hypothesis of Alzheimer's disease at 25 years
2016 Standout
Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium.
1995
Brain anomalies in children exposed prenatally to a common organophosphate pesticide
2012
Nanozymes: Classification, Catalytic Mechanisms, Activity Regulation, and Applications
2019 Standout
The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics
2002 StandoutScience
An Increased Percentage of Long Amyloid β Protein Secreted by Familial Amyloid β Protein Precursor (βApp 717 ) Mutants
1994 StandoutScience
Inactivation of the PBRM1 tumor suppressor gene amplifies the HIF-response in VHL −/− clear cell renal carcinoma
2017 StandoutNobel
Treatment with non-selective beta blockers is associated with reduced severity of systemic inflammation and improved survival of patients with acute-on-chronic liver failure
2015
Antiviral Actions of Interferons
2001 Standout
Microglia Function in the Central Nervous System During Health and Neurodegeneration
2017 Standout
The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
2011 Standout
Epigenetic regulation in pluripotent stem cells: a key to breaking the epigenetic barrier
2012 StandoutNobel
Hormones and Endocrine-Disrupting Chemicals: Low-Dose Effects and Nonmonotonic Dose Responses
2012 Standout
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
1996 Standout
Nuclear Receptor Coregulators: Cellular and Molecular Biology*
1999 Standout
Genetics and pathology of alpha-secretase site AβPP mutations in the understanding of Alzheimer's disease
2006
A multidrug resistance transporter from human MCF-7 breast cancer cells
1998 Standout
Breakpoint analysis: precise localization of genetic markers by means of nonstatistical computation using relatively few genotypes.
1995
Pathological bacterial translocation in cirrhosis: pathophysiology, diagnosis and clinical implications
2012
Genetic Restriction of HIV-1 Infection and Progression to AIDS by a Deletion Allele of the CKR5 Structural Gene
1996 StandoutScience
Targeting Glutamine Induces Apoptosis: A Cancer Therapy Approach
2015
Increased renal expression and urinary excretion of TLR 4 in acute kidney injury associated with cirrhosis
2012
Myeloid differentiation and susceptibility to HIV-1 are linked to APOBEC3 expression
2007
Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3.
1996
EASL Clinical Practice Guidelines for the management of patients with decompensated cirrhosis
2018 Standout
Works of Vikram Sharma being referenced
A Linkage Map of Human Chromosome 21: 43 PCR Markers at Average Intervals of 2.5 cM
1993
Glucocorticoid and mineralocorticoid receptor expression in the human hippocampus in major depressive disorder
2012
The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients
1996
Dinucleotide repeat polymorphism at the D14S43 locus
1991
Prevention of acute kidney injury in a rodent model of cirrhosis following selective gut decontamination is associated with reduced renal TLR4 expression
2012
Ornithine phenylacetate targets alterations in the expression and activity of glutamine synthase and glutaminase to reduce ammonia levels in bile duct ligated rats
2013
Identification of cell surface targets for HIV-1 therapeutics using genetic screens
2004
Dinucleotide repeat polymorphism at the D11S35 locus
1990
Evidence for a dynamic role of the linker histone variant H1x during retinoic acid‐induced differentiation of NT2 cells
2010
Quantitative morphological assessment reveals neuronal and glial deficits in hippocampus after a brief subtoxic exposure to chlorpyrifos in neonatal rats
2005
SS18 Together with Animal-Specific Factors Defines Human BAF-Type SWI/SNF Complexes
2012
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene
1998
Knockdown of Interleukin-1 Receptor Type-1 on Endothelial Cells Attenuated Stress-Induced Neuroinflammation and Prevented Anxiety-Like Behavior
2014
Dinucleotide repeat polymorphism at the D18S37 locus
1992