A peek behind the curtain: peer review and editorial decision making at Stroke.

Abstract:

OBJECTIVE:A better understanding of the manuscript peer-review process could improve the likelihood that research of the highest quality is funded and published. To this end, we aimed to assess consistency across reviewers' recommendations, agreement between reviewers' recommendations and editors' final decisions, and reviewer- and editor-level factors influencing editorial decisions at the journal Stroke. METHODS:We analyzed all initial original contributions submitted to Stroke from January 2004 through December 2011. All submissions were linked to the final editorial decision (accept vs reject). We assessed the level of agreement between reviewers (intraclass correlation coefficient). We compared the initial editorial decision (accept, minor revision, major revision, and reject) across reviewers' recommendations. We performed a logistic regression analysis to identify reviewer- and editor-related factors associated with acceptance as the final decision. RESULTS:Of 12,902 original submissions to Stroke during the 8-year study period, the level of agreement between reviewers was between fair and moderate (intraclass correlation coefficient = 0.55, 95% confidence interval [CI] = 0.09-0.75). Likelihood of acceptance was <5% if at least 1 reviewer recommended a rejection. In the multivariate analysis, higher reviewer-assigned priority scores were related to greater odds of acceptance (odds ratio [OR] = 26.3, 95% CI = 23.2-29.8), whereas higher number of reviewers (OR = 0.54 per additional reviewer, 95% CI = 0.50-0.59) and suggestions for reviewers by authors versus no suggestions (OR = 0.83, 95% CI = 0.73-0.94) had lesser odds of acceptance. INTERPRETATION:This analysis of the peer-review process at Stroke identified several factors that might be targeted to improve the consistency and fairness of the overall process.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Sposato LA,Ovbiagele B,Johnston SC,Fisher M,Saposnik G,Stroke Outcome Research Working Group (www.sorcan.ca).

doi

10.1002/ana.24218

subject

Has Abstract

pub_date

2014-08-01 00:00:00

pages

151-8

issue

2

eissn

0364-5134

issn

1531-8249

journal_volume

76

pub_type

杂志文章
  • T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy.

    abstract:OBJECTIVE:To determine the clinical consequences of the PMP22 point mutation, T118M, which has been previously considered to either cause an autosomal recessive form of Charcot-Marie-Tooth (CMT) disease or be a benign polymorphism. METHODS:We analyzed patients from five separate kindreds and characterized their periph...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20777

    authors: Shy ME,Scavina MT,Clark A,Krajewski KM,Li J,Kamholz J,Kolodny E,Szigeti K,Fischer RA,Saifi GM,Scherer SS,Lupski JR

    更新日期:2006-02-01 00:00:00

  • Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA.

    abstract::Two families with a point mutation in mtDNA associated with myoclonic epilepsy and ragged-red fiber disease showed pronounced clinical heterogeneity. The mothers of the two families had adult-onset myopathy with ragged-red fibers, partial deficiency of cytochrome c oxidase, and sensory neuropathy. Members of the first...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410330613

    authors: Graf WD,Sumi SM,Copass MK,Ojemann LM,Longstreth WT Jr,Shanske S,Lombes A,DiMauro S

    更新日期:1993-06-01 00:00:00

  • Neurofilament breakdown products in degenerating rat and human peripheral nerves.

    abstract::The fate of neurofilament (NF) proteins was examined in sections of nerves from rats that survived for 3 to 90 days following nerve transection, using anti-NF monoclonal antibodies and immunohistochemical techniques. The same methods were also applied to twenty-three human nerve biopsy specimens. Granular debris with ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410160312

    authors: Trojanowski JQ,Lee VM,Schlaepfer WW

    更新日期:1984-09-01 00:00:00

  • Anti-Ri: an antibody associated with paraneoplastic opsoclonus and breast cancer.

    abstract::The serum and cerebrospinal fluid (CSF) of 8 women with ataxia, 6 of whom also had eye movement abnormalities believed to be opsoclonus, were found to contain a highly specific antineuronal antibody we call anti-Ri. Seven of the 8 women also had or developed cancer: carcinoma of the breast in 5, adenocarcinoma in an a...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290303

    authors: Luque FA,Furneaux HM,Ferziger R,Rosenblum MK,Wray SH,Schold SC Jr,Glantz MJ,Jaeckle KA,Biran H,Lesser M

    更新日期:1991-03-01 00:00:00

  • Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.

    abstract::The worldwide epidemiology of Creutzfeldt-Jakob disease (CJD) is presented from an analysis of 1,435 patients. In the United States, the average annual mortality rate is at least 0.26 deaths per million. Temporal-spatial clustering of cases was not found in the United States, but reports from other countries indicate ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410050212

    authors: Masters CL,Harris JO,Gajdusek DC,Gibbs CJ Jr,Bernoulli C,Asher DM

    更新日期:1979-02-01 00:00:00

  • Increases in helper inducer T cells and activated T cells in HTLV-I-associated myelopathy.

    abstract::Using two-color flow cytometric analysis, we studied peripheral blood lymphocyte subsets in 15 patients with human T-cell lymphotropic virus type I-associated myelopathy. The percentage of CD4+ 4B4+ cells (helper inducer T cell) was significantly increased in the patients with the myelopathy, compared with 16 healthy ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410260212

    authors: Itoyama Y,Kira J,Fujii N,Goto I,Yamamoto N

    更新日期:1989-08-01 00:00:00

  • Familial myoclonic dementia masquerading as Creutzfeldt-Jakob disease.

    abstract::We describe a kindred with 7 confirmed and 2 probable cases of subacute dementia accompanied by myoclonus. The inheritance pattern is consistent with autosomal dominance and shows anticipation. The pathological changes involve marked gliosis with neuronal loss of the dorsomedial and midline thalamic nuclei, with lesse...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410200209

    authors: Little BW,Brown PW,Rodgers-Johnson P,Perl DP,Gajdusek DC

    更新日期:1986-08-01 00:00:00

  • Imaging-guided convection-enhanced delivery and gene therapy of glioblastoma.

    abstract::In a prospective phase I/II clinical study, we treated eight patients suffering from recurrent glioblastoma multiform with stereotactically guided intratumoral convection-enhanced delivery of an HSV-1-tk gene-bearing liposomal vector and systemic ganciclovir. Noninvasive identification of target tissue together with a...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1002/ana.10688

    authors: Voges J,Reszka R,Gossmann A,Dittmar C,Richter R,Garlip G,Kracht L,Coenen HH,Sturm V,Wienhard K,Heiss WD,Jacobs AH

    更新日期:2003-10-01 00:00:00

  • Normobaric hypoxia and symptoms of acute mountain sickness: Elevated brain volume and intracranial hypertension.

    abstract:OBJECTIVE:The study was undertaken to determine whether normobaric hypoxia causes elevated brain volume and intracranial pressure in individuals with symptoms consistent with acute mountain sickness (AMS). METHODS:Thirteen males age = (26 (sd 6)) years were exposed to normobaric hypoxia (12% O2 ) and normoxia (21% O2 ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24171

    authors: Lawley JS,Alperin N,Bagci AM,Lee SH,Mullins PG,Oliver SJ,Macdonald JH

    更新日期:2014-06-01 00:00:00

  • Cytosolic phospholipase A2 protein as a novel therapeutic target for spinal cord injury.

    abstract:OBJECTIVE:The objective of this study was to investigate whether cytosolic phospholipase A2 (cPLA2 ), an important isoform of PLA2 that mediates the release of arachidonic acid, plays a role in the pathogenesis of spinal cord injury (SCI). METHODS:A combination of molecular, histological, immunohistochemical, and beha...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24134

    authors: Liu NK,Deng LX,Zhang YP,Lu QB,Wang XF,Hu JG,Oakes E,Bonventre JV,Shields CB,Xu XM

    更新日期:2014-05-01 00:00:00

  • Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p.

    abstract::We describe the clinical and oculographic findings in 4 families with episodic ataxia and interictal nystagmus (EA-2) linked to chromosome 19p. Episodes varied from pure ataxia to combinations of symptoms suggesting involvement of the cerebellum, brainstem, and cortex. Some affected individuals exhibited a progressive...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410410105

    authors: Baloh RW,Yue Q,Furman JM,Nelson SF

    更新日期:1997-01-01 00:00:00

  • Conjugal multiple sclerosis: population-based prevalence and recurrence risks in offspring. Canadian Collaborative Study Group.

    abstract::From a population-based sample of 15,504 patients attending Canadian multiple sclerosis (MS) clinics, we have determined the frequency of conjugal MS and have estimated the recurrence risk in offspring of such matings. Twenty-three MS cases were found among 13,550 spouses of study probands for a crude conjugal rate of...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Ebers GC,Yee IM,Sadovnick AD,Duquette P

    更新日期:2000-12-01 00:00:00

  • Functional motor unit failure precedes neuromuscular degeneration in canine motor neuron disease.

    abstract::Hereditary canine spinal muscular atrophy (HCSMA) features rapidly progressive muscle weakness that affects muscles in an apparent proximal-to-distal gradient. In the medial gastrocnemius (MG) muscle of homozygous HCSMA animals, motor unit tetanic failure is apparent before the appearance of muscle weakness and appear...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Balice-Gordon RJ,Smith DB,Goldman J,Cork LC,Shirley A,Cope TC,Pinter MJ

    更新日期:2000-05-01 00:00:00

  • Upregulation of choline acetyltransferase activity in hippocampus and frontal cortex of elderly subjects with mild cognitive impairment.

    abstract::In Alzheimer's disease (AD), loss of cortical and hippocampal choline acetyltransferase (ChAT) activity has been correlated with dementia severity and disease duration, and it forms the basis for current therapies. However, the extent to which reductions in ChAT activity are associated with early cognitive decline has...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10069

    authors: DeKosky ST,Ikonomovic MD,Styren SD,Beckett L,Wisniewski S,Bennett DA,Cochran EJ,Kordower JH,Mufson EJ

    更新日期:2002-02-01 00:00:00

  • Perinatal risk factors in children with serious motor and mental handicaps.

    abstract::Fifty children with marked neurological abnormality manifested by moderate or severe motor disability and severe mental retardation were compared with a large control population with respect to prospectively ascertained perinatal characteristics. None of 60 prenatal factors distinguished the affected group from contro...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410020505

    authors: Nelson KB,Broman SH

    更新日期:1977-11-01 00:00:00

  • Carbamazepine and phenytoin inhibit somatostatin release from dispersed cerebral cells in culture.

    abstract::To elucidate the mechanism by which carbamazepine lowers somatostatin concentration in cerebrospinal fluid of humans, the effect of carbamazepine on secretion of this peptide was studied in rat cerebral cell cultures. Concentrations of carbamazepine within the therapeutic range (4 x 10(-5) M) inhibited spontaneous rel...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290412

    authors: Reichlin S,Mothon S

    更新日期:1991-04-01 00:00:00

  • Plasma concentrations of sodium valproate: their clinical value.

    abstract::Plasma valproate concentrations were monitored prospectively in 54 previously untreated adult patients with epilepsy. Dose and plasma concentration were highly correlated. Adverse effects were common in association with plasma levels above 100 micrograms/ml. In patients suffering tonic-clonic seizures without focal sy...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1002/ana.410140107

    authors: Turnbull DM,Rawlins MD,Weightman D,Chadwick DW

    更新日期:1983-07-01 00:00:00

  • Quantitative analysis of cortical pyramidal neurons after corpus callosotomy.

    abstract::This study quantitatively explored the dendritic/spine extent of supragranular pyramidal neurons across several cortical areas in two adult male subjects who had undergone a callosotomy several decades before death. In all cortical areas, there were numerous atypical, supragranular pyramidal neurons with elongated "ta...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10620

    authors: Jacobs B,Creswell J,Britt JP,Ford KL,Bogen JE,Zaidel E

    更新日期:2003-07-01 00:00:00

  • Levodopa induces dyskinesias in normal squirrel monkeys.

    abstract::This study assessed whether or not levodopa induces dyskinesias in normal (ie, unlesioned) squirrel monkeys. All six animals treated twice daily with levodopa (15 mg/kg with carbidopa by oral gavage) for two weeks developed choreoathetoid dyskinesias, whereas none of the vehicle-treated animals displayed any abnormal ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.1099

    authors: Togasaki DM,Tan L,Protell P,Di Monte DA,Quik M,Langston JW

    更新日期:2001-08-01 00:00:00

  • The pressure difference between eye and brain changes with posture.

    abstract:OBJECTIVE:The discovery of a posture-dependent effect on the difference between intraocular pressure (IOP) and intracranial pressure (ICP) at the level of lamina cribrosa could have important implications for understanding glaucoma and idiopathic intracranial hypertension and could help explain visual impairments in as...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24713

    authors: Eklund A,Jóhannesson G,Johansson E,Holmlund P,Qvarlander S,Ambarki K,Wåhlin A,Koskinen LO,Malm J

    更新日期:2016-08-01 00:00:00

  • Retinal nerve fiber layer axonal loss and visual dysfunction in optic neuritis.

    abstract::Axonal loss is thought to be a likely cause of persistent disability after a multiple sclerosis relapse; therefore, noninvasive in vivo markers specific for axonal loss are needed. We used optic neuritis as a model of multiple sclerosis relapse to quantify axonal loss of the retinal nerve fiber layer (RNFL) and second...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20575

    authors: Trip SA,Schlottmann PG,Jones SJ,Altmann DR,Garway-Heath DF,Thompson AJ,Plant GT,Miller DH

    更新日期:2005-09-01 00:00:00

  • Vulnerable neuronal subsets in Alzheimer's and Pick's disease are distinguished by their tau isoform distribution and phosphorylation.

    abstract::Aggregated tau proteins constitute the basic matrix of neuronal inclusions specific to numerous neurodegenerative disorders. Monodimensional and two-dimensional Western blot analyses performed on cortical brain homogenates allowed discrimination between disease-specific tau protein profiles. These observations raised ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410430209

    authors: Delacourte A,Sergeant N,Wattez A,Gauvreau D,Robitaille Y

    更新日期:1998-02-01 00:00:00

  • Single skinned muscle fibers in Duchenne muscular dystrophy generate normal force.

    abstract::We measured the intrinsic mechanical properties and protein content of single skinned muscle fibers obtained from patients who had Duchenne muscular dystrophy. To check for possible nonspecific changes caused by muscle disease per se, we also studied the properties of muscle fibers obtained from patients exhibiting se...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410270609

    authors: Horowits R,Dalakas MC,Podolsky RJ

    更新日期:1990-06-01 00:00:00

  • Relapsing and remitting human immunodeficiency virus-associated leukoencephalomyelopathy.

    abstract::We describe a 33-year-old homosexual man with a steroid-responsive, remitting and relapsing leukoencephalopathy associated with recent human immunodeficiency virus type 1 (HIV-1) seroconversion. Biopsy of a parieto-occipital lesion revealed demyelination and astrogliosis with focal necrosis. Detailed investigations de...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410310107

    authors: Berger JR,Tornatore C,Major EO,Bruce J,Shapshak P,Yoshioka M,Houff S,Sheremata W,Horton GF,Landy H

    更新日期:1992-01-01 00:00:00

  • Adipocytokines and the risk of ischemic stroke: the PRIME Study.

    abstract:OBJECTIVE:Adipocytokines are hormones secreted from adipose tissue that possibly link adiposity and the risk of cardiovascular disease, but limited prospective data exist on plasma adipocytokines and ischemic stroke risk. We investigated associations and predictive properties of 4 plasma adipocytokines, namely resistin...

    journal_title:Annals of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1002/ana.22669

    authors: Prugger C,Luc G,Haas B,Arveiler D,Machez E,Ferrieres J,Ruidavets JB,Bingham A,Montaye M,Amouyel P,Yarnell J,Kee F,Ducimetiere P,Empana JP,PRIME Study Group.

    更新日期:2012-04-01 00:00:00

  • Focal cerebral ischemia in the rat: topography of hemodynamic and histopathological changes.

    abstract::We studied local cerebral blood flow, as measured by autoradiography with digital image processing and by tissue morphology, in six rats 4 hours after occlusion of the proximal middle cerebral artery. A consistent, three-dimensional pattern of graded reductions in local cerebral blood flow involved the affected hemisp...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410150608

    authors: Tyson GW,Teasdale GM,Graham DI,McCulloch J

    更新日期:1984-06-01 00:00:00

  • Kearns-Sayre syndrome with reduced plasma and cerebrospinal fluid folate.

    abstract::A young woman with Kearns-Sayre syndrome and progressive central nervous system deterioration over 15 years had decreased plasma and cerebrospinal fluid folate levels while receiving phenytoin for a seizure disorder. A muscle biopsy showed a "ragged red fiber" myopathy with reduced muscle carnitine and mitochondrial e...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410130620

    authors: Allen RJ,DiMauro S,Coulter DL,Papadimitriou A,Rothenberg SP

    更新日期:1983-06-01 00:00:00

  • A randomized trial of plasma exchange in acute central nervous system inflammatory demyelinating disease.

    abstract::There are no established treatments for patients with acute, severe neurological deficits caused by multiple sclerosis or other inflammatory demyelinating diseases of the central nervous system who fail to recover after treatment with high-dose corticosteroids. We conducted a randomized, sham-controlled, double-masked...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/1531-8249(199912)46:6<878::aid-ana10>3.0.c

    authors: Weinshenker BG,O'Brien PC,Petterson TM,Noseworthy JH,Lucchinetti CF,Dodick DW,Pineda AA,Stevens LN,Rodriguez M

    更新日期:1999-12-01 00:00:00

  • Intracranial hypertension associated with unruptured cerebral arteriovenous malformations.

    abstract::Only 6 patients with intracranial hypertension associated with unruptured cerebral arteriovenous malformations have been reported. We report 6 additional patients seen at the Cleveland Clinic during the past 10 years. The average age was 28 years (range, 19-44 years); 4 were women. Symptoms and signs included papilled...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410270504

    authors: Chimowitz MI,Little JR,Awad IA,Sila CA,Kosmorsky G,Furlan AJ

    更新日期:1990-05-01 00:00:00

  • Impaired glial glutamate transport in a mouse tuberous sclerosis epilepsy model.

    abstract::Excessive astrocytosis in cortical tubers in tuberous sclerosis complex (TSC) suggests that astrocytes may be important for epileptogenesis in TSC. We previously demonstrated that astrocyte-specific Tsc1 gene inactivation in mice (Tsc1 cKO mice) results in progressive epilepsy. Here, we report that glutamate transport...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10648

    authors: Wong M,Ess KC,Uhlmann EJ,Jansen LA,Li W,Crino PB,Mennerick S,Yamada KA,Gutmann DH

    更新日期:2003-08-01 00:00:00