(Q54431091)

29 May 2018

title

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus. (English)

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29 May 2018

genome-wide association study

main subject

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6

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Bjarni V. Halldórsson

7

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Lynne J Hocking

13

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Millan S Patel

18

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Serena Scollen

19

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Cyrus Cooper

25

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William D. Leslie

30

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Robert N. Luben

41

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Carolina Medina-Gomez

42

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L. Adrienne Cupples

53

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Jonathan Reeve

58

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David Karasik

60

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Douglas P. Kiel

66

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Fernando Rivadeneira

67

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Dalila Pinto

Dalila Pinto

55

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Unnur Styrkarsdottir

Unnur Styrkarsdottir

3

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José M Olmos

José M Olmos

33

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Unnur Þorsteinsdóttir

59

Unnur Thorsteinsdottir

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29 May 2018

65

John P A Ioannidis

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57

Stephen W Scherer

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12

Göran Hallmans

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11

Gudmar Thorleifsson

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21

Stella Trompet

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62

Kari Stefansson

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Albert Hofman

49

Albert Hofman

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Natasja M van Schoor

22

Natasja M van Schoor

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29 May 2018

André Uitterlinden

63

André G Uitterlinden

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Joyce B J van Meurs

47

Joyce B J van Meurs

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Eline Slagboom

37

P Eline Slagboom

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J Wouter Jukema

50

J Wouter Jukema

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Paul Lips

31

Paul Lips

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Christian Marshall

54

Christian R Marshall

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Stephen K Kaptoge

10

Stephen K Kaptoge

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Karen A Jameson

15

Karen A Jameson

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Roman S Lorenc

32

Roman S Lorenc

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29 May 2018

Stuart H Ralston

64

Stuart H Ralston

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Marcin Kruk

16

Marcin Kruk

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29 May 2018

Ling Oei

1

Ling Oei

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José A Riancho

36

José A Riancho

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Kannabiran Nandakumar

44

Kannabiran Nandakumar

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Huibert Pols

51

Huibert A P Pols

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Ian Ford

26

Ian Ford

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29 May 2018

author name string

Yi-Hsiang Hsu

2

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29 May 2018

Bert H Eussen

4

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29 May 2018

Annelies de Klein

5

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29 May 2018

Ching-Ti Liu

8

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Nerea Alonso

9

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Lise Bjerre Husted

14

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Joshua R Lewis

17

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Olle Svensson

20

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29 May 2018

Kun Zhu

23

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David Goltzman

27

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29 May 2018

Jesús González-Macías

28

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29 May 2018

Bente Lomholt Langdahl

29

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Ulrika Pettersson-Kymmer

34

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David M Reid

35

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29 May 2018

Carmen Garcia-Ibarbia

38

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Thorvaldur Ingvarsson

39

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Hrefna Johannsdottir

40

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Pascal Arp

43

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Stefan Th Palsson

45

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Gunnar Sigurdsson

46

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29 May 2018

Yanhua Zhou

48

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Richard L Prince

52

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29 May 2018

Daisuke Sato

56

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J Brent Richards

61

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Karol Estrada

68

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29 May 2018

Brendan M Buckley

24

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29 May 2018

language of work or name

English

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publication date

16 December 2013

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29 May 2018

Journal of Medical Genetics

published in

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29 May 2018

volume

51

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29 May 2018

issue

2

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29 May 2018

page(s)

122-131

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29 May 2018

The use of clinical risk factors enhances the performance of BMD in the prediction of hip and osteoporotic fractures in men and women.

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Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk

21 January 2018

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An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits

21 January 2018

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Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.

21 January 2018

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

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Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

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Copy-number variations associated with neuropsychiatric conditions

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Rare chromosomal deletions and duplications increase risk of schizophrenia

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Structural variation of chromosomes in autism spectrum disorder

21 January 2018

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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

21 January 2018

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Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis

21 January 2018

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Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women.

21 January 2018

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

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Population analysis of large copy number variants and hotspots of human genetic disease

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Functional impact of global rare copy number variation in autism spectrum disorders

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment

21 January 2018

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21 January 2018

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21 January 2018

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10.1136/JMEDGENET-2013-102064

21 January 2018

Identifiers

DOI

1 reference

29 May 2018

PubMed ID

24343915

1 reference

29 May 2018