(Q28943501)

14 March 2017

title

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density (English)

1 reference

14 March 2017

author

Unnur Þorsteinsdóttir

23

0 references

Martin den Heijer

11

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Patrick Sulem

7

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Gudmar Thorleifsson

1

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Kári Stefánsson

24

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Augustine Kong

22

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Unnur Styrkarsdottir

5

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Thorunn Rafnar

15

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G. Bragi Walters

object named as

G. Bragi Walters

4

0 references

Daníel F. Guðbjartsson

6

object named as

Daniel F. Gudbjartsson

1 reference

14 March 2017

21

Runolfur Palsson

1 reference

14 March 2017

20

Olafur S. Indridason

1 reference

14 March 2017

Hilma Holm

2

1 reference

14 March 2017

Vidar Edvardsson

3

1 reference

14 March 2017

Bjarni V. Halldorsson

8

1 reference

14 March 2017

Femmie de Vegt

9

1 reference

14 March 2017

Frank C. H. d'Ancona

10

1 reference

14 March 2017

Leifur Franzson

12

1 reference

14 March 2017

Claus Christiansen

13

1 reference

14 March 2017

Peter Alexandersen

14

1 reference

14 March 2017

Kristleifur Kristjansson

16

1 reference

14 March 2017

Gunnar Sigurdsson

17

1 reference

14 March 2017

Lambertus A. Kiemeney

18

1 reference

14 March 2017

Magnus Bodvarsson

19

1 reference

14 March 2017

language of work or name

English

0 references

publication date

1 August 2009

1 reference

14 March 2017

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14 March 2017

volume

41

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14 March 2017

issue

8

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14 March 2017

page(s)

926–930

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14 March 2017

1 reference

New sequence variants associated with bone mineral density

21 April 2017

1 reference

Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites

21 April 2017

1 reference

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

21 April 2017

1 reference

Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement

21 April 2017

1 reference

A second generation human haplotype map of over 3.1 million SNPs

21 April 2017

1 reference

Genomic control for association studies

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.404

Genetics of gene expression and its effect on disease

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.404

A common inversion under selection in Europeans

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG.404

Genetic analyses in a sample of individuals with high or low BMD shows association with multiple Wnt pathway genes

21 April 2017

1 reference

12 December 2020

1 reference

12 December 2020

Kidney stones: pathophysiology and medical management.

1 reference

12 December 2020

Bone mineral density and urine calcium excretion among subjects with and without nephrolithiasis

1 reference

12 December 2020

High incidence of kidney stones in Icelandic children.

1 reference

12 December 2020

A novel endonuclease IV post-PCR genotyping system

1 reference

12 December 2020

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

1 reference

12 December 2020

Common variants in the region around Osterix are associated with bone mineral density and growth in childhood

1 reference

12 December 2020

Age- and gender-specific reference values of estimated GFR in Caucasians: the Nijmegen Biomedical Study.

1 reference

12 December 2020

Metabolic Risk Factors in Pediatric and Adult Calcium Oxalate Urinary Stone Formers: Is There Any Difference?

1 reference

12 December 2020

Ambulatory evaluation of nephrolithiasis: an update of a 1980 protocol.

1 reference

12 December 2020

Association between two mu-opioid receptor gene (OPRM1) haplotype blocks and drug or alcohol dependence

1 reference

12 December 2020

1 reference

12 December 2020

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration

1 reference

12 December 2020

The diagnosis of osteoporosis

1 reference

12 December 2020

Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins.

1 reference

12 December 2020

Idiopathic hypercalciuria and hyperuricosuria: family prevalence of nephrolithiasis

1 reference

12 December 2020

A prospective study of recurrence rate and risk factors for recurrence after a first renal stone

1 reference

12 December 2020

A twin study of genetic and dietary influences on nephrolithiasis: a report from the Vietnam Era Twin (VET) Registry

1 reference

12 December 2020

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke

1 reference

12 December 2020

Structure and function of claudins.

1 reference

12 December 2020

Primer3 on the WWW for general users and for biologist programmers

1 reference

12 December 2020

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

1 reference

12 December 2020

Links between cardiovascular disease and osteoporosis in postmenopausal women: serum lipids or atherosclerosis per se?

1 reference

12 December 2020

Multiple genetic loci for bone mineral density and fractures

1 reference

12 December 2020

Statistical aspects of the analysis of data from retrospective studies of disease

1 reference

12 December 2020

Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C>T affects mRNA stability

1 reference

12 December 2020

Genetics of hypercalciuric nephrolithiasis: renal stone disease

1 reference

12 December 2020

Bone buffering of acid and base in humans

1 reference

12 December 2020

Claudin-8 modulates paracellular permeability to acidic and basic ions in MDCK II cells

1 reference

12 December 2020

Metabolic evaluation of patients with recurrent idiopathic calcium nephrolithiasis

1 reference

12 December 2020

Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss

1 reference

12 December 2020

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

1 reference

12 December 2020