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citing journals

Top Articles

#TitleJournalYearCitations
1The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataBrain Imaging and Behavior2014696
2Myasthenia GravisNew England Journal of Medicine2016644
3Identification of common variants associated with human hippocampal and intracranial volumesNature Genetics2012594
4EFNS guidelines on the diagnosis and management of European Lyme neuroborreliosisEuropean Journal of Neurology2010585
5Genome-wide association studies establish that human intelligence is highly heritable and polygenicMolecular Psychiatry2011571
6Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysisLancet Psychiatry,the2017565
7Are 90% of deaths from cancer caused by metastases?Cancer Medicine2019536
8Myasthenia gravisNature Reviews Disease Primers2019421
9Permanent Neonatal Diabetes due to Mutations in KCNJ11 Encoding Kir6.2Diabetes2004350
10The impact of frailty on ICU and 30-day mortality and the level of care in very elderly patients (≥ 80 years)Intensive Care Medicine2017311
11Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunctionNature Genetics2006296
12Efficacy of faecal microbiota transplantation for patients with irritable bowel syndrome in a randomised, double-blind, placebo-controlled studyGut2020291
13Myasthenia gravis — autoantibody characteristics and their implications for therapyNature Reviews Neurology2016286
14Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre studyMultiple Sclerosis Journal2015249
15A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyNature Genetics2015245
16Perforated peptic ulcerLancet, The2015240
17ESTES guidelines: acute mesenteric ischaemiaEuropean Journal of Trauma and Emergency Surgery2016240
18Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus documentOrphanet Journal of Rare Diseases2015239
19Disease‐modifying treatments for multiple sclerosis – a review of approved medicationsEuropean Journal of Neurology2016238
20Oncogenic PIK3CA-driven mammary tumors frequently recur via PI3K pathway–dependent and PI3K pathway–independent mechanismsNature Medicine2011231
21The contribution of frailty, cognition, activity of daily life and comorbidities on outcome in acutely admitted patients over 80 years in European ICUs: the VIP2 studyIntensive Care Medicine2020230
22Daily Duration of Vitamin D Synthesis in Human Skin with Relation to Latitude, Total Ozone, Altitude, Ground Cover, Aerosols and Cloud ThicknessPhotochemistry and Photobiology2005229
23Fetal cardiac output, distribution to the placenta and impact of placental compromiseUltrasound in Obstetrics and Gynecology2006222
24Identification of six new susceptibility loci for invasive epithelial ovarian cancerNature Genetics2015221
25Middle cerebral artery blood flow velocities and pulsatility index and the cerebroplacental pulsatility ratio: longitudinal reference ranges and terms for serial measurementsUltrasound in Obstetrics and Gynecology2007220
26Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanomaNature Genetics2015218
27Continuing Stability of Center Differences in Pediatric Diabetes Care: Do Advances in Diabetes Treatment Improve Outcome?Diabetes Care2007194
28Long-term quality of life in patients with vestibular schwannoma: an international multicenter cross-sectional study comparing microsurgery, stereotactic radiosurgery, observation, and nontumor controlsJournal of Neurosurgery2015192
29EANO guideline on the diagnosis and treatment of vestibular schwannomaNeuro-Oncology2020190
30Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX , SOX4 , and IRX3Proceedings of the National Academy of Sciences of the United States of America2010189
31Discriminating Variable Test and Selectivity Ratio Plot: Quantitative Tools for Interpretation and Variable (Biomarker) Selection in Complex Spectral or Chromatographic ProfilesAnalytical Chemistry2009188
32Transanal total mesorectal excision for rectal cancer has been suspended in NorwayBritish Journal of Surgery2019188
33Toward a Consensus on Centralization in SurgeryAnnals of Surgery2018187
34Periprosthetic Femoral Fracture within Two Years After Total Hip ReplacementJournal of Bone and Joint Surgery - Series A2014185
35Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 DiabetesDiabetes2008184
36The status of intensive care medicine research and a future agenda for very old patients in the ICUIntensive Care Medicine2017182
37Survival and cause of death in multiple sclerosis: a 60-year longitudinal population studyJournal of Neurology, Neurosurgery and Psychiatry2017180
38Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)Molecular Psychiatry2014178
39The genomic landscape and evolution of endometrial carcinoma progression and abdominopelvic metastasisNature Genetics2016174
40Acute bacterial conjunctivitisActa Ophthalmologica2008168
41Peli1 promotes microglia-mediated CNS inflammation by regulating Traf3 degradationNature Medicine2013156
42Brain atrophy and disability progression in multiple sclerosis patients: a 10-year follow-up studyJournal of Neurology, Neurosurgery and Psychiatry2014155
43Fetal growth restriction and birth defects with newer and older antiepileptic drugs during pregnancyJournal of Neurology2014152
44Profiles of Genomic Instability in High-Grade Serous Ovarian Cancer Predict Treatment OutcomeClinical Cancer Research2012150
45The Complement Control-Related Genes CSMD1 and CSMD2 Associate to SchizophreniaBiological Psychiatry2011149
46A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitusHuman Genetics2006147
47Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23–related hypophosphatemia, dental anomalies, and ectopic calcificationJournal of Bone and Mineral Research2013144
48Effects of varying dietary content of fermentable short‐chain carbohydrates on symptoms, fecal microenvironment, and cytokine profiles in patients with irritable bowel syndromeNeurogastroenterology and Motility2017144
49Point of Care Ultrasound: A WFUMB Position PaperUltrasound in Medicine and Biology2017143
50Congenital Stromal Dystrophy of the Cornea Caused by a Mutation in the Decorin Gene2005140