Genetics of dementia (Q56069696)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

title

Genetics of dementia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

John B Kwok

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

author name string

Clement T Loy

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Anne M Turner

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

language of work or name

English

0 references

publication date

6 August 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

volume

383

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

issue

9919

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

page(s)

828-840

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23927914%20AND%20SRC:MED&resulttype=core&format=json

Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study

7 March 2020

cites work

1 reference

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7 January 2021

Genetic linkage studies

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7 January 2021

How to use an article about genetic association: A: Background concepts

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7 January 2021

Genetic risk prediction--are we there yet?

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7 January 2021

Retrospective diagnosis of dementia using an informant interview based on the Brief Cognitive Rating Scale.

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7 January 2021

Frontotemporal dementia and Alzheimer's disease: retrospective differentiation using information from informants

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7 January 2021

Frontotemporal dementia presenting as schizophrenia-like psychosis in young people: clinicopathological series and review of cases.

1 reference

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7 January 2021

Clinical and biomarker changes in dominantly inherited Alzheimer's disease

1 reference

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7 January 2021

The diagnosis of young-onset dementia.

1 reference

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7 January 2021

Knowledge of and attitudes about Alzheimer disease genetics: report of a pilot survey and two focus groups.

1 reference

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7 January 2021

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

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7 January 2021

The diagnosis of dementia due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease

1 reference

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7 January 2021

Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors

1 reference

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7 January 2021

Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update

1 reference

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7 January 2021

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

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7 January 2021

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum

1 reference

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7 January 2021

Early onset familial Alzheimer's disease: Mutation frequency in 31 families.

1 reference

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7 January 2021

Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Sequence analysis of presenilin-1 gene mutation in Japanese Alzheimer's disease patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Correlating familial Alzheimer's disease gene mutations with clinical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Genetic insights in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The amyloid hypothesis for Alzheimer's disease: a critical reappraisal

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Amyloid-independent mechanisms in Alzheimer's disease pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Statement on Use of Apolipoprotein E Testing for Alzheimer Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

1 reference

7 January 2021

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

1 reference

7 January 2021

TREM2 Variants in Alzheimer's Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Mutations in TREM2 lead to pure early-onset dementia without bone cysts.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Risk of dementia among white and African American relatives of patients with Alzheimer disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Diagnostic criteria for the behavioral variant of frontotemporal dementia (bvFTD): current limitations and future directions

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Neuroimaging in frontotemporal lobar degeneration--predicting molecular pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Clinicopathological correlates in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Phenotypic signatures of genetic frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The logopenic variant of primary progressive aphasia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Primary progressive aphasia: a tale of two syndromes and the rest

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Semantic dementia: demography, familial factors and survival in a consecutive series of 100 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Genetic Causes of Frontotemporal Degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The heritability and genetics of frontotemporal lobar degeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Tau alteration and neuronal degeneration in tauopathies: mechanisms and models

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Potential mechanisms of progranulin-deficient FTLD

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Evidence for an oligogenic basis of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Pick bodies in a family with presenilin-1 Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease course.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

An algorithm for genetic testing of frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Neuropsychological deficits in frontotemporal dementia and Alzheimer's disease: a meta-analytic review

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Familial aggregation in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Transmissible spongiform encephalopathies.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Prion disease genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Amyloid imaging in distinguishing atypical prion disease from Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The natural history of Alzheimer disease: a longitudinal presymptomatic and symptomatic study of a familial cohort.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

1 reference

7 January 2021

Detection of Huntington's disease decades before diagnosis: the Predict-HD study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Levodopa responsive parkinsonism in an adult with Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The autosomal recessive cerebellar ataxias

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Cognitive findings in spinocerebellar ataxia type 2: relationship to genetic and clinical variables.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Cognitive deficits in Machado-Joseph disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Cognitive functioning in neurologically symptomatic and asymptomatic forms of Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Clinical molecular diagnosis of Wilson disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

1 reference

7 January 2021

The adult form of Niemann-Pick disease type C.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

New agents and approaches to treatment in Niemann-Pick type C disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Genetic disorders affecting white matter in the pediatric age.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

1 reference

7 January 2021

Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Complex single gene disorders and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Single-gene neurological disorders in South Wales: an epidemiological study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Recent advances in the genetics of dementia with lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Familial aggregation of dementia with Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Identification of families with cortical Lewy body disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Dementia in Parkinson's disease: a 20-year neuropsychological study (Sydney Multicentre Study).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The genetics of Parkinson's syndromes: a critical review

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Glucocerebrosidase mutations are an important risk factor for Lewy body disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Genetics of dementia: update and guidelines for the clinician

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

International Huntington Association and the World Federation of Neurology Research Group on Huntington's Chorea. Guidelines for the molecular genetics predictive test in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

The Columbia-Suicide Severity Rating Scale: initial validity and internal consistency findings from three multisite studies with adolescents and adults

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Exome sequencing as a tool for Mendelian disease gene discovery

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Exome sequencing reveals VCP mutations as a cause of familial ALS

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021

Individual genomes on the horizon

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2813%2960630-3

7 January 2021