(Q24648667)

30

0 references

Stefania Bandinelli

22

0 references

Luigi Ferrucci

21

0 references

Heinz Erich Wichmann

31

0 references

Dalia Kasperaviciute

58

0 references

Gabriella Restagno

3

0 references

Adriano Chiò

1

0 references

Sampath Arepalli

10

0 references

Michael Sendtner

61

0 references

Francesca Valentino

Francesca Valentino

39

0 references

Stefania Battistini

Stefania Battistini

34

0 references

Claudia Caponnetto

Claudia Caponnetto

36

0 references

Jessica Mandrioli

Jessica Mandrioli

45

0 references

Sonja Scholz

Sonja W Scholz

4

0 references

Andrea Calvo

Andrea Calvo

32

0 references

Mario Sabatelli

Mario Sabatelli

43

0 references

Fabio Macciardi

Fabio Macciardi

24

0 references

Kevin Talbot

Kevin Talbot

52

0 references

Gianluigi Mancardi

Giovanni Luigi Mancardi

37

0 references

Gabriele Siciliano

Gabriele Siciliano

49

0 references

Stephen Chanock

27

Stephen J Chanock

0 references

John Anthony Hardy

67

John Hardy

0 references

Andrew Singleton

66

Andrew Singleton

0 references

Cynthia Crews

17

Cynthia Crews

0 references

David J. Hunter

29

David J Hunter

0 references

Gabriele Mora

7

Gabriele Mora

0 references

Maria Rosaria Monsurrò

40

Maria Rosaria Monsurrò

0 references

Jack Guralnik

23

Jack Guralnik

0 references

Bryan Traynor

68

Bryan J Traynor

0 references

Dena G. Hernandez

20

Dena Hernandez

0 references

Gioacchino Tedeschi

41

Gioacchino Tedeschi

0 references

Angela F Britton

9

Angela Britton

0 references

Michael Marmot

12

Michael Nalls

0 references

J Raphael Gibbs

11

J Raphael Gibbs

0 references

Nicole Washecka

19

Nicole Washecka

0 references

Patrizia Sola

46

Patrizia Sola

0 references

Federica Lombardo

5

Federica Lombardo

0 references

Lucie Bruijn

63

Lucie Bruijn

0 references

Shiao-Lin Lai

6

Shiao-Lin Lai

0 references

author name string

Jennifer C Schymick

2

0 references

Hon-Chung Fung

8

0 references

Stephen Berger

13

0 references

Lydia Coulter Kwee

14

0 references

Eugene Z Oddone

15

0 references

Jinhui Ding

16

0 references

Ian Rafferty

18

0 references

Federica Torri

25

0 references

Sara Lupoli

26

0 references

Gilles Thomas

28

0 references

Roberto Mutani

33

0 references

Fabio Giannini

35

0 references

Vincenzo La Bella

38

0 references

Kalliopi Marinou

42

0 references

Amelia Conte

44

0 references

Fabrizio Salvi

47

0 references

Ilaria Bartolomei

48

0 references

Cecilia Carlesi

50

0 references

Richard W Orrell

51

0 references

Zachary Simmons

53

0 references

James Connor

54

0 references

Erik P Pioro

55

0 references

Travis Dunkley

56

0 references

Dietrich A Stephan

57

0 references

Elizabeth M Fisher

59

0 references

Sibylle Jabonka

60

0 references

Marcus Beck

62

0 references

Jeffrey Rothstein

64

0 references

Silke Schmidt

describes a project that uses

65

0 references

language of work or name

English

0 references

publication date

15 April 2009

0 references

published in

Human Molecular Genetics

0 references

volume

18

0 references

issue

8

0 references

page(s)

1524-32

0 references

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

A second generation human haplotype map of over 3.1 million SNPs

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

PLINK: a tool set for whole-genome association and population-based linkage analyses

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Haploview: analysis and visualization of LD and haplotype maps

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Multiple loci identified in a genome-wide association study of prostate cancer

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Risk alleles for multiple sclerosis identified by a genomewide study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Replicating genotype-phenotype associations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Genes and Environmental Exposures in Veterans with Amyotrophic Lateral Sclerosis: the GENEVA study. Rationale, study design and demographic characteristics.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

The National Registry of Veterans with amyotrophic lateral sclerosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Methods for handling multiple testing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Genetics of familial amyotrophic lateral sclerosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Genetics of sporadic amyotrophic lateral sclerosis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Genome-wide association studies: theoretical and practical concerns

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Subsystems contributing to the decline in ability to walk: bridging the gap between epidemiology and geriatric practice in the InCHIANTI study.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

British motor neuron disease twin study

28 September 2017

1 reference

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Genetics. The elusive ALS genes

28 September 2017

1 reference

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A genome-wide association study of sporadic ALS in a homogenous Irish population.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

A survey of genetic human cortical gene expression

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664150

Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19193627

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of SOD1 mutations in the Italian ALS population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19193627

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDP059

1 reference

1 reference

1 reference

PubMed publication ID

19193627

1 reference