(Q35563817)

8 August 2017

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title

Genetic approaches to stature, pubertal timing, and other complex traits (English)

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8 August 2017

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1 reference

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https://api.crossref.org/works/10.1016/S1096-7192(03)00107-0

23 March 2024

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https://api.crossref.org/works/10.1016/S1096-7192(03)00107-0

23 March 2024

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https://api.crossref.org/works/10.1016/S1096-7192(03)00107-0

23 March 2024

2

Joel N. Hirschhorn

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14567953

23 March 2024

author name string

Mark R. Palmert

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14567953

23 March 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14567953

23 March 2024

publication date

1 September 2003

1 reference

full work available at URL

8 August 2017

https://api.elsevier.com/content/article/PII:S1096719203001070?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S1096-7192(03)00107-0

https://api.elsevier.com/content/article/PII:S1096719203001070?httpAccept=text/plain

23 March 2024

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https://api.crossref.org/works/10.1016/S1096-7192(03)00107-0

Molecular Genetics and Metabolism

23 March 2024

published in

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8 August 2017

volume

80

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8 August 2017

issue

1-2

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8 August 2017

page(s)

1-10

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Quantitative genetic analysis of longitudinal trends in height: preliminary results from the Louisville Twin Study.

8 August 2017

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A cross-sectional examination of height, weight, and body mass index in adult twins

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7 January 2021

The genetic contribution to stature

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7 January 2021

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

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7 January 2021

Twin children in The Gambia: evidence for genetic regulation of physical characteristics in the presence of sub-optimal nutrition

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7 January 2021

Age at menarche. Genetic and environmentalinfluences

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7 January 2021

Secondary sexual characteristics and menses in young girls seen in office practice: a study from the Pediatric Research in Office Settings network

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7 January 2021

Estimating genetic influences on the age-at-menarche: a survival analysis approach

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7 January 2021

Genetic correlates of menarcheal age: a multivariate twin study

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7 January 2021

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7 January 2021

The Rate of Growth and Maturing of Twins

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Genetic dissection of complex traits

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7 January 2021

Variations on a theme: cataloging human DNA sequence variation

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7 January 2021

Variation in the timing of puberty: clinical spectrum and genetic investigation

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7 January 2021

Effects of recombinant leptin therapy in a child with congenital leptin deficiency.

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7 January 2021

Molecular basis of combined pituitary hormone deficiencies

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7 January 2021

Molecular-pathogenetic classification of genetic disorders of the skeleton

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7 January 2021

Genetic disorders of human growth

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7 January 2021

A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor

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7 January 2021

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

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7 January 2021

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

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7 January 2021

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

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7 January 2021

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

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7 January 2021

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

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7 January 2021

Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

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7 January 2021

Congenital leptin deficiency is associated with severe early-onset obesity in humans

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7 January 2021

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

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7 January 2021

A leptin missense mutation associated with hypogonadism and morbid obesity.

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7 January 2021

Molecular basis for familial isolated growth hormone deficiency

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7 January 2021

Laron dwarfism and mutations of the growth hormone-receptor gene

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7 January 2021

Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism

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7 January 2021

Haploinsufficiency of NSD1 causes Sotos syndrome

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7 January 2021

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

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7 January 2021

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

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7 January 2021

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature

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7 January 2021

How many diseases does it take to map a gene with SNPs?

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7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

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7 January 2021

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

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7 January 2021

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer

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7 January 2021

Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families

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7 January 2021

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

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7 January 2021

Identification of the breast cancer susceptibility gene BRCA2

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7 January 2021

Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity

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7 January 2021

Once and Again—Issues Surrounding Replication in Genetic Association Studies

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7 January 2021

Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women

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7 January 2021

Hyperandrogenism and manifesting heterozygotes for 21-hydroxylase deficiency

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7 January 2021

On the allelic spectrum of human disease

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7 January 2021

Characterization of single-nucleotide polymorphisms in coding regions of human genes

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7 January 2021

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

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7 January 2021

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

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7 January 2021

Replication validity of genetic association studies

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7 January 2021

A comprehensive review of genetic association studies

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7 January 2021

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

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7 January 2021

The future of genetic studies of complex human diseases

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7 January 2021

Diagnosis of late puberty.

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7 January 2021

6 Delayed adolescence

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7 January 2021

Clinical review 6: Diagnosis and management of delayed puberty

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7 January 2021

Etiologies of Late Puberty

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7 January 2021

Pedigree analysis of constitutional delay of growth and maturation: determination of familial aggregation and inheritance patterns

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7 January 2021

Major recessive gene(s) with considerable residual polygenic effect regulating adult height: confirmation of genomewide scan results for chromosomes 6, 9, and 12.

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7 January 2021

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900107-0

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7 January 2021

Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families

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7 January 2021

Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

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7 January 2021

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

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7 January 2021

Genomewide scans of complex human diseases: true linkage is hard to find

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7 January 2021

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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7 January 2021

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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7 January 2021

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

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7 January 2021

The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

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7 January 2021

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

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7 January 2021

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

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7 January 2021

Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

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7 January 2021

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

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7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

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7 January 2021

Comprehensive human genetic maps: individual and sex-specific variation in recombination

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7 January 2021

A high-resolution recombination map of the human genome

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7 January 2021

Accessing genetic variation: genotyping single nucleotide polymorphisms

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7 January 2021

Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height

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7 January 2021

Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components

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7 January 2021

Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups

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7 January 2021

A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature

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7 January 2021

Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes

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7 January 2021

Association study designs for complex diseases

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7 January 2021

Candidate-gene approaches for studying complex genetic traits: practical considerations

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7 January 2021

Genetic Polymorphisms and Disease

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7 January 2021

Tests and estimates of allelic association in complex inheritance

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7 January 2021

Testing for population subdivision and association in four case-control studies

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7 January 2021

Association mapping in structured populations

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7 January 2021

Genomic control for association studies

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7 January 2021

Detecting association in a case-control study while correcting for population stratification

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7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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7 January 2021

Estrogen-metabolizing gene polymorphisms, but not estrogen receptor-alpha gene polymorphisms, are associated with the onset of menarche in healthy postmenopausal Japanese women

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7 January 2021

High-resolution haplotype structure in the human genome

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7 January 2021

The structure of haplotype blocks in the human genome

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7 January 2021

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

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7 January 2021

Haplotype tagging for the identification of common disease genes

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7 January 2021

Human genome. HapMap launched with pledges of $100 million

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7 January 2021

Age at menarche as a fitness trait: nonadditive genetic variance detected in a large twin sample

16

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Linkage strategies for genetically complex traits. I. Multilocus models

23 March 2024

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The TDT and other family-based tests for linkage disequilibrium and association

23 March 2024

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A polymorphism in the CYP17 gene increases the risk of breast cancer

23 March 2024

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23 March 2024

Identifiers

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8 August 2017

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