PubRank

Stefan Johansson

Author PubWeight™ 55.20‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children. PLoS Med 2011 3.94
2 Maternal obesity and risk of preterm delivery. JAMA 2013 3.14
3 Timing of pharmacological treatment for patent ductus arteriosus and risk of secondary surgery, death or bronchopulmonary dysplasia: a population-based cohort study of extremely preterm infants. Neonatology 2014 2.80
4 Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. Nat Genet 2005 2.22
5 Familial diarrhea syndrome caused by an activating GUCY2C mutation. N Engl J Med 2012 2.04
6 Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolism. Am J Hum Genet 2010 1.95
7 Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes. Nat Genet 2013 1.91
8 FTO, type 2 diabetes, and weight gain throughout adult life: a meta-analysis of 41,504 subjects from the Scandinavian HUNT, MDC, and MPP studies. Diabetes 2011 1.75
9 Risks for low intellectual performance related to being born small for gestational age are modified by gestational age. Pediatrics 2006 1.54
10 Can association between preterm birth and autism be explained by maternal or neonatal morbidity? Pediatrics 2009 1.41
11 Noninvasive acoustic cell trapping in a microfluidic perfusion system for online bioassays. Anal Chem 2007 1.40
12 Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD. Neuropsychopharmacology 2009 1.33
13 Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23-related hypophosphatemia, dental anomalies, and ectopic calcification. J Bone Miner Res 2013 1.26
14 Genetic and shared environmental factors do not confound the association between birth weight and hypertension: a study among Swedish twins. Circulation 2007 1.23
15 MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing. Orphanet J Rare Dis 2013 1.16
16 SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. Am J Hum Genet 2013 1.05
17 Virtual colleagues, virtually colleagues--physicians' use of Twitter: a population-based observational study. BMJ Open 2013 1.04
18 Diabetes and pancreatic exocrine dysfunction due to mutations in the carboxyl ester lipase gene-maturity onset diabetes of the young (CEL-MODY): a protein misfolding disease. J Biol Chem 2011 0.99
19 On-chip fluorescence-activated cell sorting by an integrated miniaturized ultrasonic transducer. Anal Chem 2009 0.96
20 STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity. Orphanet J Rare Dis 2014 0.94
21 Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes. Hum Genet 2009 0.93
22 Attention-deficit/hyperactivity disorder symptoms in offspring of mothers with impaired serotonin production. Arch Gen Psychiatry 2010 0.92
23 A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry. Diabetes 2006 0.91
24 Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay. PLoS One 2013 0.91
25 Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder. Biol Psychiatry 2009 0.90
26 The number of tandem repeats in the carboxyl-ester lipase (CEL) gene as a risk factor in alcoholic and idiopathic chronic pancreatitis. Pancreatology 2012 0.89
27 Variants of anterior segment dysgenesis and cerebral involvement in a large family with a novel COL4A1 mutation. Am J Ophthalmol 2013 0.86
28 Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). BMC Med Genet 2011 0.84
29 Renal volume and function in school-age children born preterm or small for gestational age. Pediatr Nephrol 2008 0.84
30 Pancreatic exocrine dysfunction in maturity-onset diabetes of the young type 3. Diabetes Care 2007 0.83
31 Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature. BMC Genet 2014 0.83
32 Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients. PLoS One 2013 0.82
33 Glutamate cysteine ligase (GCL) and self reported depression: an association study from the HUNT. J Affect Disord 2011 0.82
34 DISC1 in adult ADHD patients: an association study in two European samples. Am J Med Genet B Neuropsychiatr Genet 2013 0.82
35 Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes. Diabetes 2009 0.82
36 Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populations. Am J Med Genet B Neuropsychiatr Genet 2011 0.81
37 High Maternal Body Mass Index in Early Pregnancy and Risks of Stillbirth and Infant Mortality-A Population-Based Sibling Study in Sweden. Am J Epidemiol 2016 0.80
38 DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders. Neuropsychopharmacology 2011 0.80
39 Effective mixing of laminar flows at a density interface by an integrated ultrasonic transducer. Lab Chip 2008 0.79
40 DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS One 2012 0.79
41 Glycogenin-2 is dispensable for liver glycogen synthesis and glucagon-stimulated glucose release. J Clin Endocrinol Metab 2015 0.78
42 Surface acoustic wave induced particle manipulation in a PDMS channel--principle concepts for continuous flow applications. Biomed Microdevices 2012 0.77
43 Trapping of microparticles in the near field of an ultrasonic transducer. Ultrasonics 2004 0.77
44 No association between the serotonin transporter gene polymorphism 5-HTTLPR and cyclothymic temperament as measured by TEMPS-A. J Affect Disord 2010 0.77
45 Temperature and trapping characterization of an acoustic trap with miniaturized integrated transducers--towards in-trap temperature regulation. Ultrasonics 2013 0.76
46 The importance of echocardiography and an individual approach to patent ductus arteriosus treatment in extremely preterm infants. Neonatology 2015 0.75
47 [Correction and comments to an article published earlier in Lakartidningen. The article "Valve-sparing surgery should be considered primarily" has been scrutinized by KI]. Lakartidningen 2009 0.75
48 [Molecular diagnostics in diabetes mellitus]. Tidsskr Nor Laegeforen 2005 0.75
49 [Our responsibility to reflect on the madness]. Lakartidningen 2015 0.75
50 Comparison of Walking and Traveling-Wave Piezoelectric Motors as Actuators in Kinesthetic Haptic Devices. IEEE Trans Haptics 2016 0.75
51 [Children's food--for long-term health]. Lakartidningen 2014 0.75
52 [In Process Citation]. Lakartidningen 2016 0.75
53 [Progress in diabetes genetics]. Tidsskr Nor Laegeforen 2010 0.75
54 Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis. Am J Hum Genet 2017 0.75
55 Comparison of Walking and Traveling-Wave Piezoelectric Motors as Actuators in Kinesthetic Haptic Devices. IEEE Trans Haptics 2016 0.75
56 [In Process Citation]. Lakartidningen 2015 0.75