Citation Impact
Citing Papers
The myth of language universals: Language diversity and its importance for cognitive science
2009 Standout
The Case For More Active Policy Attention To Health Promotion
2002 Standout
A unified mixed-model method for association mapping that accounts for multiple levels of relatedness
2005 Standout
Association Mapping in Structured Populations
2000 Standout
Experimental models of inflammatory bowel disease
1995 Standout
Glutamate uptake
2001 Standout
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
1996 Standout
Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q
1999
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
2007 Standout
Principal components analysis corrects for stratification in genome-wide association studies
2006 Standout
Genetic Epidemiology of Major Depression: Review and Meta-Analysis
2000 Standout
Autism: Towards an Integration of Clinical, Genetic, Neuropsychological, and Neurobiological Perspectives
1996 Standout
Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series
2010 Standout
Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence
2004 Standout
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
1995 Standout
Juvenile Myoclonic Epilepsy: A 5‐Year Prospective Study
1994
No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF)
2004
Environmental and Heritable Factors in the Causation of Cancer — Analyses of Cohorts of Twins from Sweden, Denmark, and Finland
2000 Standout
Evidence for Gradients of Human Genetic Diversity Within and Among Continents
2004 StandoutNobel
A Turning Point in Schizophrenia Genetics
1997
Predictors for long‐term seizure outcome in juvenile myoclonic epilepsy: 25–63 years of follow‐up
2012
Congenital structural anomalies in offspring of women with epilepsy—a population-based cohort study in Finland
2005
Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration
2007 Standout
Update on the pathophysiology of the epilepsies
2000
GENETICS OF MIGRAINE
1997
Strengthening the Reporting of Observational Studies in Epidemiology (STROBE)
2007 Standout
Linkage of familial combined hyperlipidaemia to chromosome 1q21–q23
1998
Association of TNF2, a TNF-α Promoter Polymorphism, With Septic Shock Susceptibility and Mortality
1999 Standout
Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and elaboration
2014 Standout
Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration
2007 Standout
Insulin Resistance and the Polycystic Ovary Syndrome: Mechanism and Implications for Pathogenesis*
1997 Standout
Interneurons of the hippocampus
1998 Standout
ILAE Official Report: A practical clinical definition of epilepsy
2014 Standout
An introduction to markers, quantitative trait loci (QTL) mapping and marker-assisted selection for crop improvement: The basic concepts
2005 Standout
The Future of Genetic Studies of Complex Human Diseases
1996 StandoutScience
Genetic Dissection of Complex Traits
1994 StandoutScience
Is the underlying cause of epilepsy a major prognostic factor for recurrence?
1998 Standout
Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications
2012 Standout
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Cellular and molecular basis of epilepsy
1994
Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region
1996 StandoutScience
Defining Computational Thinking for Mathematics and Science Classrooms
2015 Standout
Works of M. Durner being referenced
Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6
1991
The genetics of idiopathic generalized epilepsies of adolescent onset
1995
Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods.
1992
Family Studies on the Genetics of Juvenile Myoclonic Epilepsy (Epilepsy with Impulsive Petit Mal)
1989
Is there a genetic relationship between epilepsy and birth defects?
1992
Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients
1991