PubRank

D Hannequin

Author PubWeight™ 77.11‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet 2013 9.46
2 Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum. Am J Hum Genet 1999 3.14
3 Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease. Neurology 2009 2.46
4 APOE and Alzheimer disease: a major gene with semi-dominant inheritance. Mol Psychiatry 2011 2.31
5 Valosin-containing protein gene mutations: clinical and neuropathologic features. Neurology 2006 2.00
6 High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease. Mol Psychiatry 2012 1.84
7 Usefulness of transcranial color-coded sonography in the diagnosis of cerebral vasospasm. Stroke 1999 1.67
8 Variations in the APP gene promoter region and risk of Alzheimer disease. Neurology 2007 1.64
9 Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update. J Med Genet 2005 1.60
10 Pediatric cerebral aneurysms. J Neurosurg 2001 1.57
11 Giant cervical epidural veins after lumbar puncture in a case of intracranial hypotension. AJNR Am J Neuroradiol 2000 1.55
12 Mutations of the presenilin I gene in families with early-onset Alzheimer's disease. Hum Mol Genet 1995 1.55
13 Brain spect perfusion of frontotemporal dementia associated with motor neuron disease. Neurology 2007 1.41
14 Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex. Am J Hum Genet 1997 1.27
15 Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. Hum Mol Genet 1998 1.27
16 Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype. Hum Mutat 2000 1.27
17 Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Mol Psychiatry 2012 1.20
18 Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation. Neurology 2000 1.20
19 Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease. Arch Neurol 1998 1.09
20 Outcome in 43 patients with distal anterior cerebral artery aneurysms. Stroke 1997 1.06
21 Oropharyngeal dysphagia in amyotrophic lateral sclerosis alters quality of life. J Oral Rehabil 2012 0.99
22 Midsagittal MR measurements of the corpus callosum in healthy subjects and diseased patients: a prospective survey. AJNR Am J Neuroradiol 1993 0.96
23 Clinical imaging and neuropathological correlations in an unusual case of cerebrotendinous xanthomatosis. Clin Neuropathol 2010 0.96
24 A large pedigree with early-onset Alzheimer's disease: clinical, neuropathologic, and genetic characterization. Neurology 1995 0.94
25 Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes. J Med Genet 2005 0.94
26 The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease. Genomics 1995 0.94
27 Measurement of voice onset time in dysarthric patients: methodological considerations. Folia Phoniatr Logop 2001 0.91
28 A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years. Neuroreport 1996 0.90
29 Intrafamilial diversity of phenotype associated with app duplication. Neurology 2008 0.89
30 Tentorial edge traumatic aneurysm of the superior cerebellar artery. Case report. J Neurosurg 1997 0.88
31 De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group. J Med Genet 1998 0.88
32 Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation. Cephalalgia 2008 0.87
33 Anatomy of executive deficit following ruptured anterior communicating artery aneurysm. Eur J Neurol 2009 0.86
34 Submental sensitive transcutaneous electrical stimulation (SSTES) at home in neurogenic oropharyngeal dysphagia: a pilot study. Ann Phys Rehabil Med 2011 0.86
35 No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group. J Med Genet 1996 0.84
36 Dysarthria and orofacial apraxia in corticobasal degeneration. Mov Disord 2000 0.84
37 APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population. Eur J Hum Genet 2000 0.83
38 Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation. J Neurol Neurosurg Psychiatry 2007 0.83
39 [Clinical assessment of dysarthria: presentation and validation of a method]. Rev Neurol (Paris) 1998 0.82
40 Tangier disease phenotype diversity in dizygous twin sisters. Rev Neurol (Paris) 2010 0.82
41 Picture confrontation oral naming: performance differences between aphasics and normals. Brain Lang 1996 0.82
42 Characteristics of familial aggregation in early-onset Alzheimer's disease: evidence of subgroups. Am J Med Genet 1995 0.82
43 Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives. Am J Med Genet 1995 0.82
44 The neurobiological basis of time estimation and temporal order. Rev Neurosci 1999 0.82
45 Causes of morbidity and mortality after ruptured aneurysm surgery in a series of 230 patients. The importance of control angiography. Stroke 1995 0.81
46 [Cortico-basal degeneration]. Rev Neurol (Paris) 1999 0.80
47 Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family. Acta Neuropathol 2005 0.80
48 Calculation and number processing in mild Alzheimer's disease. J Clin Exp Neuropsychol 1995 0.80
49 Alpha2-macroglobulin gene and Alzheimer's disease: confirmation of association by haplotypes analyses. Ann Neurol 2000 0.80
50 [Continuous partial epilepsy disclosing diabetes mellitus]. Rev Neurol (Paris) 1994 0.80
51 Clozapine for the treatment of psychosis in Parkinson's disease: a review. Acta Neurol Scand 1996 0.79
52 Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group. Am J Med Genet 1996 0.79
53 Marchiafava-Bignami disease. A case studied by CT and MR imaging. Neuroradiology 1986 0.79
54 [Isolated truncular paralysis of the musculocutaneous nerve of the upper limb]. Rev Chir Orthop Reparatrice Appar Mot 2000 0.79
55 No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients. Schizophr Res 1998 0.78
56 [Stress-induced pituitary apoplexy in 2 phases]. Neurochirurgie 1995 0.78
57 Clinical screening of oropharyngeal dysphagia in patients with ALS. Ann Phys Rehabil Med 2012 0.77
58 [Stiff-person syndrome and other neurological disorders associated with anti-GAD antibodies]. Rev Med Interne 2009 0.77
59 [Development of a model to study the anti-edema properties of Ginkgo biloba extract]. Presse Med 1986 0.77
60 [Saccadic latencies and unilateral spatial neglect caused by parietal lesions]. Rev Neurol (Paris) 1996 0.77
61 Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population. Eur J Hum Genet 2001 0.76
62 Angiographic cerebral vasospasm and delayed ischemic deficit on anterior part of the circle of Willis. Usefulness of transcranial Doppler. Neurochirurgie 2002 0.76
63 [Intermittent sea-saw nystagmus successfully treated with clonazepam]. Rev Neurol (Paris) 1995 0.76
64 No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease. J Neurol Neurosurg Psychiatry 1997 0.76
65 [Musical hallucinosis following infarction of the right middle cerebral artery]. Rev Neurol (Paris) 2001 0.76
66 [Cervico-occipital injury and bilateral paralysis of cranial nerve XII. Apropos of a case]. J Radiol 1986 0.76
67 [Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]. Rev Neurol (Paris) 2005 0.76
68 [Stroke and iridodonesis revealing a homocystinuria caused by a compound heterozygous mutation of cystathionine beta-synthase]. Rev Neurol (Paris) 2008 0.76
69 Diversity of patterns of improvement in confrontation naming rehabilitation: some tentative hypotheses. J Commun Disord 1997 0.75
70 Is there still discussion when the mandible is dislocated? Arch Neurol 1998 0.75
71 [Dementia: new concepts, new goals]. Rev Neurol (Paris) 2013 0.75
72 [Bilateral C8 meningoradiculitis in infectious mononucleosis]. Presse Med 1996 0.75
73 Detailed neuropsychological evaluation in a patient with Floating Harbor syndrome. J Clin Exp Neuropsychol 2012 0.75
74 Superior interhemispheric approach for midline meningioma from the anterior cranial base. Neurochirurgie 2011 0.75
75 [Genetics of dominant autosomal forms of Alzheimer disease: 3 genes and one phenotype. Groupe de Recherche Francais sur la Maladie d'Alzheimer]. Rev Neurol (Paris) 1996 0.75
76 [Chronic parkinsonian syndrome after 10 years of repeated insecticide spraying]. Rev Neurol (Paris) 2008 0.75
77 [An aphasic reader]. Rev Neurol (Paris) 2008 0.75
78 [Stroke and cornea verticillata revealing Fabry's disease in a female]. Rev Neurol (Paris) 2011 0.75
79 Anorectal manometric anomalies in seven patients with frontal lobe brain damage. Dig Dis Sci 1990 0.75
80 [Multiple cervical arterial dissections in two brothers: fibro-muscular dysplasia or connective tissue disease?]. Rev Neurol (Paris) 2008 0.75
81 [A case of atypical Miller-Fisher syndrome treated with intravenous immunoglobulins]. Ann Med Interne (Paris) 1996 0.75
82 [Two confusion scales]. Rev Neurol (Paris) 2001 0.75
83 [Cerebrovascular complication in non-bacterial thrombotic endocarditis. Value of cardiac transesophageal ultrasonography]. Presse Med 1997 0.75
84 [Intracerebral hematoma due to a mild form of Von Willebrand's disease]. Presse Med 1986 0.75
85 [Confusional state and agitation]. Rev Prat 2000 0.75
86 [Therapeutic efficacy during active phases of multiple sclerosis: gait analysis and comparison with the EDSS score]. Rev Neurol (Paris) 2001 0.75
87 [Involvement of the major hypoglossal nerve disclosing dissection of internal carotid artery]. Ann Otolaryngol Chir Cervicofac 1996 0.75
88 [Anti-Ri paraneoplastic syndrome associated with ophtalmoplegia, blepharospasm and palilalia]. Rev Neurol (Paris) 2005 0.75
89 [Alzheimer disease: autosomal dominant forms]. Rev Neurol (Paris) 2008 0.75
90 [Flash-pattern visual evoked potentials and limited lesions of the occipital lobe]. Rev Electroencephalogr Neurophysiol Clin 1985 0.75
91 [Naming impairment for man-made objects in a case of herpes encephalitis]. Rev Neurol (Paris) 1998 0.75
92 [The assessment of long-term memory and semantic knowledge]. Rev Neurol (Paris) 2000 0.75
93 [Dissociation of visual evoked responses to hemi-field or full-field flash-checkerboard stimulation]. Rev Electroencephalogr Neurophysiol Clin 1984 0.75
94 [Vasospasm after rupture of aneurysms of the anterior communicating artery. Sensitivity and specificity of transcranial Doppler]. Neurochirurgie 1995 0.75
95 [Akathisia induced by low doses of neuroleptics after a pallidal infarction]. Presse Med 1996 0.75
96 [Spontaneous thrombosis of cerebral arteriovenous malformation]. J Radiol 1997 0.75
97 Asessment of paraneoplastic limbic encephalitis in testicular cancer. Clin Oncol (R Coll Radiol) 2003 0.75
98 Hemidystonia as initial manifestation of sporadic Creutzfeldt-Jakob disease. Eur J Neurol 2006 0.75
99 [Treatment of psychotic complications of Parkinson disease with clozapine]. Presse Med 1997 0.75
100 [Sporadic cerebral amyloidotic angiopathy]. Rev Neurol (Paris) 2006 0.75
101 Worsening of psychotic symptoms by clozapine in Parkinson's disease. Lancet 1994 0.75
102 [EEG recordings during episodes of palinacousis and palinopsia]. Rev Neurol (Paris) 1997 0.75
103 [Evaluation of motor speech function in the diagnosis of various forms of dysarthria]. Rev Neurol (Paris) 2000 0.75
104 Exacerbation of multiple sclerosis during therapy that included brain extracts. Med J Aust 1988 0.75
105 [Argyrophilic grain disease: synergistic component of dementia?]. Rev Neurol (Paris) 2009 0.75
106 [Palinopsia associated with partial seizures secondary to right parietal hemorrhage]. Ann Med Interne (Paris) 1998 0.75
107 [Colonic perforation disclosing primary amyloidosis]. Ann Med Interne (Paris) 1988 0.75
108 [Palinacousis with hemianacusia caused by left temporal lesion]. Rev Neurol (Paris) 1995 0.75
109 [Myasthenic syndrome induced by lithium]. Presse Med 2000 0.75
110 [Marchiafava-Bignami disease with favorable development]. Rev Neurol (Paris) 1986 0.75
111 [Late neurologic complications of galactosemia: study of 3 cases]. Rev Neurol (Paris) 1995 0.75