Citation Impact
Citing Papers
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
2015 StandoutNobel
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
Genetic Influences on Brain Gene Expression in Rats Selected for Tameness and Aggression
2014 StandoutNobel
Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism
2024 StandoutNobel
Crystal Structure of the Second LNS/LG Domain from Neurexin 1α
2006 StandoutNobel
TREM2 in CNS homeostasis and neurodegenerative disease
2015
EGFR Antagonists in Cancer Treatment
2008 Standout
Mitochondrial energy generation disorders: genes, mechanisms, and clues to pathology
2017
Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia
2002
Stromal fibroblasts in cancer initiation and progression
2004 StandoutNature
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
1995
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
2006 Standout
Linkage and associated studies of schizophrenia
2000
Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts
2000
Genetic linkage and association between chromosome 1q and working memory function in schizophrenia
2002
Revisiting the TCA cycle: signaling to tumor formation
2011
Endocrine aspects of organelle stress — cell non-autonomous signaling of mitochondria and the ER
2015
Applying genomic and transcriptomic advances to mitochondrial medicine
2021
Disruption of two novel genes by a translocation co-segregating with schizophrenia
2000 Standout
A Systematic Review of the Prevalence of Schizophrenia
2005
Hallmarks of aging: An expanding universe
2023 Standout
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
1996 Standout
Shaping human telomeres: from shelterin and CST complexes to telomeric chromatin organization
2021 Nobel
Mitochondrial Dysfunction and Neurodegeneration in Lysosomal Storage Disorders
2017
Keap1-null mutation leads to postnatal lethality due to constitutive Nrf2 activation
2003
Scatter-factor and semaphorin receptors: cell signalling for invasive growth
2002
Rnd Proteins Function as RhoA Antagonists by Activating p190 RhoGAP
2003
Mechanisms of nuclear reprogramming by eggs and oocytes: a deterministic process?
2011 StandoutNobel
MicroRNA-92a is a circadian modulator of neuronal excitability in Drosophila
2017 StandoutNobel
Evolution of the neocortex: a perspective from developmental biology
2009
Positional Cloning of Disease Genes: Advantages of Genetic Isolates
1999
Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis
2011 StandoutNature
Mitochondria: In Sickness and in Health
2012 Standout
TREM2 Lipid Sensing Sustains the Microglial Response in an Alzheimer’s Disease Model
2015 Standout
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
The telomere syndromes
2012 Nobel
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Mechanisms of mitochondrial diseases
2011
Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22
2000
Rho GTPases in cell biology
2002 StandoutNature
Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010
2013 Standout
Molecular genetics of the Finnishdisease heritage
1999
MiR-980 Is a Memory Suppressor MicroRNA that Regulates the Autism-Susceptibility Gene A2bp1
2016
Therapy for mitochondrial disorders: Little proof, high research activity, some promise
2011
The semaphorins: versatile regulators of tumour progression and tumour angiogenesis
2008
A pathophysiological framework of hippocampal dysfunction in ageing and disease
2011
Rethinking schizophrenia
2010 StandoutNature
Migraine — Current Understanding and Treatment
2002 Standout
How can we realize the promise of personalized antidepressant medicines?
2008
Persistent postsurgical pain: risk factors and prevention
2006 Standout
Cellular and Molecular Mechanisms of Pain
2009 StandoutNobel
Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype
2002
Functional organization of the hippocampal longitudinal axis
2014 StandoutNobel
Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic Factor
2013 Standout
Understanding the Intersections between Metabolism and Cancer Biology
2017 Standout
Rho and Rac Take Center Stage
2004 Standout
Semaphorin-mediated axonal guidance via Rho-related G proteins
2001
The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
2003 Standout
Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging
2010
The Hallmarks of Aging
2013 Standout
Oxidative stress and neurodegeneration: where are we now?
2006 Standout
The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia
2002
Extensive Linkage Disequilibrium in Small Human Populations in Eurasia
2002 StandoutNobel
Molecular mechanisms and clinical applications of angiogenesis
2011 StandoutNature
Targeting endothelial and tumor cells with semaphorins
2007
The molecular neurobiology of depression
2008 StandoutNature
Nasu–Hakola Disease (Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy—PLOSL): A Dementia Associated with Bone Cystic Lesions. From Clinical to Genetic and Molecular Aspects
2004
A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
2017 Standout
Molecular genetics of migraine
2009
The Inheritance of Neuropsychological Dysfunction in Twins Discordant for Schizophrenia
2000
Tumor Angiogenesis
2008 Standout
Use of population isolates for mapping complex traits
2000
GENETICS OF MIGRAINE
1997
Linkage Disequilibrium and the Search for Complex Disease Genes
2000
Soluble amyloid precursor protein (APP) regulates transthyretin and Klotho gene expression without rescuing the essential function of APP
2010 StandoutNobel
Proteomic Analysis of Mouse Oocytes Reveals 28 Candidate Factors of the “Reprogrammome”
2011
RhoE Binds to ROCK I and Inhibits Downstream Signaling
2003
Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice
2005
Separating endogenous ancient DNA from modern day contamination in a Siberian Neandertal
2014 StandoutNobel
Lysosomal activity regulatesCaenorhabditis elegansmitochondrial dynamics through vitamin B12 metabolism
2020 StandoutNobel
Dialogue between E. coli free radical pathways and the mitochondria of C. elegans
2015 StandoutNobel
Transthyretin protects Alzheimer's mice from the behavioral and biochemical effects of Aβ toxicity
2008
DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms
2009
Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice
2012
The Human Genome Project and Its Impact on Psychiatry
2002
Spermidine in health and disease
2018 StandoutScience
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
How neuroinflammation contributes to neurodegeneration
2016 StandoutScience
Muscle mitohormesis promotes cellular survival via serine/glycine pathway flux
2014
Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene
2003 StandoutScience
Inositol hexakisphosphate suppresses excitatory neurotransmission via synaptotagmin-1 C2B domain in the hippocampal neuron
2012 StandoutNobel
Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice
2011
Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22
2000 Science
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
2001
The synapse proteome and phosphoproteome: a new paradigm for synapse biology
2006
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline
2010 StandoutNobel
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
2001 Standout
Mitochondrial dysfunction remodels one-carbon metabolism in human cells
2016
Pain Genes?: Natural Variation and Transgenic Mutants
2000
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
2012 StandoutNobel
The Structure of Haplotype Blocks in the Human Genome
2002 StandoutScience
Molecular Mechanisms of Axon Guidance
2002 Science
LINKAGE ANALYSIS IN PSYCHIATRIC DISORDERS : The Emerging Picture
2002
Works of Iiris Hovatta being referenced
Chromosome 4 workshop summary: Sixth World Congress on Psychiatric Genetics, Bonn, Germany, October 6-10, 1998
1999
Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set
1998
A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci
1999
Assignment of a Novel Locus for Autosomal Recessive Congenital Ichthyosis to Chromosome 19p13.1-p13.2
2000
Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo
2000
Familial Migraine: Exclusion of the Susceptibility Gene from the Reported Locus of Familial Hemiplegic Migraine on 19p
1994
Mutations in CTC1 , Encoding the CTS Telomere Maintenance Complex Component 1, Cause Cerebroretinal Microangiopathy with Calcifications and Cysts
2012
Glyoxalase 1 and glutathione reductase 1 regulate anxiety in mice
2005 Nature
Molecular genetics of anxiety in mice and men
2008
Human microRNAs miR-22, miR-138-2, miR-148a, and miR-488 Are Associated with Panic Disorder and Regulate Several Anxiety Candidate Genes and Related Pathways
2010
Anxiety genetics – findings from cross-species genome-wide approaches
2013
Accuracy of register-based schizophrenia diagnoses in a genetic study
1998
Batten disease (JNCL) is linked to disturbances in mitochondrial, cytoskeletal, and synaptic compartments
2006
The semaphorin 3A receptor may directly regulate the activity of small GTPases
2000
Mitochondrial myopathy induces a starvation-like response
2010
Downregulation of SRF–FOS–JUNB pathway in fumarate hydratase deficiency and in uterine leiomyomas
2009
Adult mouse brain gene expression patterns bear an embryologic imprint
2005
Sixth World Congress of Psychiatric Genetics X chromosome workshop
1999
Report of the Chromosome 5 Workshop of the Sixth World Congress on Psychiatric Genetics
1999
Antagonistic Effects of Rnd1 and RhoD GTPases Regulate Receptor Activity in Semaphorin 3A-Induced Cytoskeletal Collapse
2002
Assignment of the Locus for PLO-SL, a Frontal-Lobe Dementia with Bone Cysts, to 19q13
1998
Schizophrenia in the genetic isolate of Finland
1997
Concordance for Sex and the Pseudoautosomal Gene Hypothesis Revisited: No Evidence of Increased Sex Concordance in a Nationwide Finnish Sample of Siblings With Paternally Derived Schizophrenia
1998
Schizophrenia in the genetic isolate of Finland
1997
Chromosomes 1, 2, and 7 workshop
1999