(Q36232888)

12 August 2017

Height-reducing variants and selection for short stature in Sardinia (English)

1 reference

12 August 2017

22

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12 August 2017

23

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12 August 2017

26

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12 August 2017

34

David Schlessinger

0 references

Serena Sanna

4

Serena Sanna

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Antonella Mulas

5

Antonella Mulas

0 references

Magdalena Zoledziewska

1

Magdalena Zoledziewska

1 reference

12 August 2017

Maristella Steri

6

0 references

Matteo Floris

Matteo Floris

12

0 references

Alessandro P Delitala

Alessandro Delitala

14

0 references

Michele Marongiu

Michele Marongiu

9

0 references

Maria Pina Concas

Maria Pina Concas

15

0 references

Ginevra Biino

Ginevra Biino

17

0 references

Andrea Angius

Andrea Angius

31

0 references

Francesco Cucca

Francesco Cucca

35

0 references

Diego Ortega-Del Vecchyo

11

Diego Ortega Del Vecchyo

0 references

Kirk E. Lohmueller

20

Kirk E Lohmueller

1 reference

12 August 2017

Carlo Sidore

2

1 reference

12 August 2017

Charleston W K Chiang

3

1 reference

12 August 2017

Fabio Busonero

7

1 reference

12 August 2017

Joseph H Marcus

8

1 reference

12 August 2017

Andrea Maschio

10

1 reference

12 August 2017

Antonella Meloni

13

1 reference

12 August 2017

Federico Murgia

16

1 reference

12 August 2017

Simona Vaccargiu

18

1 reference

12 August 2017

Ramaiah Nagaraja

19

1 reference

12 August 2017

UK10K consortium

21

1 reference

12 August 2017

Ioanna Tachmazidou

24

1 reference

12 August 2017

George Dedoussis

25

1 reference

12 August 2017

Understanding Society Scientific Group

27

1 reference

12 August 2017

Sergio Uzzau

28

1 reference

12 August 2017

Chris Jones

29

1 reference

12 August 2017

Robert Lyons

30

1 reference

12 August 2017

Gonçalo R Abecasis

32

1 reference

12 August 2017

John Novembre

33

1 reference

12 August 2017

language of work or name

English

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publication date

14 September 2015

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12 August 2017

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12 August 2017

47

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12 August 2017

11

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12 August 2017

1352-1356

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.3403

12 August 2017

0 references

cites work

Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Massive migration from the steppe was a source for Indo-European languages in Europe

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Defining the role of common variation in the genomic and biological architecture of adult human height

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Ancient human genomes suggest three ancestral populations for present-day Europeans

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

A population genetic signal of polygenic adaptation

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Genetic variants regulating immune cell levels in health and disease.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Low-pass DNA sequencing of 1200 Sardinians reconstructs European Y-chromosome phylogeny

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Evidence of widespread selection on standing variation in Europe at height-associated SNPs

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Hundreds of variants clustered in genomic loci and biological pathways affect human height

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Variance component model to account for sample structure in genome-wide association studies

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Parental origin of sequence variants associated with complex diseases

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Widespread genomic signatures of natural selection in hominid evolution

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Common variants at ten loci influence QT interval duration in the QTGEN Study

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Morphological evolution is accelerated among island mammals

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Heritability of cardiovascular and personality traits in 6,148 Sardinians

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

selscan: an efficient multithreaded program to perform EHH-based scans for positive selection

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

The little women of Loja--growth hormone-receptor deficiency in an inbred population of southern Ecuador

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Secular trend and regional differences in the stature of Italians

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4627578

Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

22 September 2018

1 reference

Relative effect of genetic and environmental factors on body height: differences across birth cohorts among Finnish men and women

21 January 2018

1 reference

12 December 2020

The syndrome of familial dwarfism and high plasma immunoreactive human growth hormone

1 reference

12 December 2020

Serum GH binding protein activities identifies the heterozygous carriers for Laron type dwarfism

1 reference

12 December 2020

Effects of heterozygosity for the E180 splice mutation causing growth hormone receptor deficiency in Ecuador on IGF-I, IGFBP-3, and stature

1 reference

12 December 2020

Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma

1 reference

7 January 2021

inferred from DOI database lookup

Co-regulated transcriptional networks contribute to natural genetic variation in Drosophila sleep

1 reference

7 January 2021

inferred from DOI database lookup

Evolution of Island Mammals

1 reference

7 January 2021

inferred from DOI database lookup

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.3403

1 reference

release_butzejl4hfeevirs7ywondiw4q

12 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/butzejl4hfeevirs7ywondiw4q

24 November 2022

mapped directly with Wikidata item

1 reference

12 August 2017

PubMed publication ID

26366551

1 reference