American Journal of Human Genetics

ISSN: 0002-9297

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American Journal of Human Genetics Q1 Unclaimed

Cell Press United States
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

American Journal of Human Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 330. It has a price of 4598 €. It has an SJR impact factor of 4,516 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 4,516.

American Journal of Human Genetics focuses its scope in these topics and keywords: mutations, gene, syndrome, caused, genetic, mitochondrial, disease, association, pigmentosa, prediction, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Price

4598 €

Inmediate OA

0 €

Embargoed OA

0 €

Non OA

Metrics

American Journal of Human Genetics

4,516

SJR Impact factor

330

H Index

168

Total Docs (Last Year)

531

Total Docs (3 years)

8773

Total Refs

4022

Total Cites (3 years)

500

Citable Docs (3 years)

6.82

Cites/Doc (2 years)

52.22

Ref/Doc

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Aims and Scope


mutations, gene, syndrome, caused, genetic, mitochondrial, disease, association, pigmentosa, prediction, oxidase, identification, variant, variants, xlinked, progressive, neonatalonset, mutation, mental, congenital, disorder, dominant, eastern, ectodermal, encoding, heart, identifies, loci, locus, maps, mecp,



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A Tobit Variance-Component Method for Linkage Analysis of Censored Trait Data

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Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype Correlations

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Atypical Forms of Incontinentia Pigmenti in Male Individuals Result from Mutations of a Cytosine Tract in Exon 10 of NEMO (IKK- gamma)

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Goosecoid-Like Sequences and the Smallest Region of Deletion Overlap in DiGeorge and Velocardiofacial Syndromes

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The Quantitative LOD Score: Test Statistic and Sample Size for Exclusion and Linkage of Quantitative Traits in Human Sibships

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Reply to Gill

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NCALD Antisense Oligonucleotide Therapy in Addition to Nusinersen further Ameliorates Spinal Muscular Atrophy in Mice

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Paraoxonase-Gene Polymorphisms Associated with Coronary Heart Disease: Support for the Oxidative Damage Hypothesis?

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Familial Multiple-System Tauopathy with Presenile Dementia Is Localized to Chromosome 17

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