(Q55055441)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22190362%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Rare variants in the CYP27B1 gene are associated with multiple sclerosis (English)

1 reference

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19 January 2020

0 references

13

1 reference

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19 January 2020

Zameel Cader

3

1 reference

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Antonio J Berlanga-Taylor

19 January 2020

7

1 reference

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19 January 2020

Adam E Handel

8

1 reference

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19 January 2020

author name string

Sreeram V Ramagopalan

1

1 reference

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19 January 2020

David A Dyment

2

1 reference

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19 January 2020

Katie M Morrison

4

1 reference

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19 January 2020

Giulio Disanto

5

1 reference

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19 January 2020

Julia M Morahan

6

1 reference

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19 January 2020

Gabriele C De Luca

9

1 reference

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19 January 2020

A Dessa Sadovnick

10

1 reference

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19 January 2020

Pierre Lepage

11

1 reference

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19 January 2020

Alexandre Montpetit

12

1 reference

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19 January 2020

publication date

1 December 2011

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19 January 2020

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19 January 2020

volume

70

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19 January 2020

issue

6

1 reference

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19 January 2020

page(s)

881-886

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Environmental factors and multiple sclerosis.

19 January 2020

cites work

1 reference

Risk alleles for multiple sclerosis in multiplex families.

21 January 2018

1 reference

A genome-wide scan in forty large pedigrees with multiple sclerosis

21 January 2018

1 reference

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

21 January 2018

1 reference

Risk alleles for multiple sclerosis identified by a genomewide study

21 January 2018

1 reference

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

21 January 2018

1 reference

Uncovering the roles of rare variants in common disease through whole-genome sequencing

21 January 2018

1 reference

Exome sequencing identifies the cause of a mendelian disorder

21 January 2018

1 reference

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

21 January 2018

1 reference

The Sequence Alignment/Map format and SAMtools

21 January 2018

1 reference

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

21 January 2018

1 reference

A method and server for predicting damaging missense mutations

21 January 2018

1 reference

Fast and accurate short read alignment with Burrows-Wheeler transform

21 January 2018

1 reference

Vitamin D 1alpha-hydroxylase gene mutations in patients with 1alpha-hydroxylase deficiency

21 January 2018

1 reference

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

21 January 2018

1 reference

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

21 January 2018

1 reference

Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 families

21 January 2018

1 reference

A novel G102E mutation of CYP27B1 in a large family with vitamin D-dependent rickets type 1

21 January 2018

1 reference

A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution

21 January 2018

1 reference

Serum 25-hydroxyvitamin D levels and risk of multiple sclerosis

21 January 2018

1 reference

Timing of birth and risk of multiple sclerosis: population based study

21 January 2018

1 reference

21 January 2018

1 reference

Short- and long-term outcome of patients with pseudo-vitamin D deficiency rickets treated with calcitriol.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.22678

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22190362%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference