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Journal Photo for Nature Genetics
Peer reviewed only Open Access

Nature Genetics (NG)

Publisher : Springer Nature
Biochemistry Genetics Molecular Biology
Claim Your Journal Get PRC Visit Website
e-ISSN 1546-1718
p-ISSN 1061-4036
Issue Frequency Monthly
Est. Year 1992
Mobile 18007774643
Language English
APC YES
Impact Factor Assignee Google Scholar
Email tiago.faial@us.nature.com

Journal Descriptions

Nature Genetics is a monthly journal publishing the best research from across the field of genetics, with our broad scope ensuring that work published reaches the widest possible audience. All editorial decisions are made by a team of full-time professional editors. Our international standard serial number (ISSN) is 1061-4036. Our electronic international standard serial number (EISSN) is 1546-1718. Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation.

Nature Genetics (NG) is :-

  • International, Peer-Reviewed, Open Access, Refereed, Biochemistry, Genetics, Molecular Biology , Online or Print , Monthly Journal

  • UGC Approved, ISSN Approved: P-ISSN P-ISSN: 1061-4036, E-ISSN: 1546-1718, Established: 1992,
  • Does Not Provide Crossref DOI

  • Not indexed in Scopus, WoS, DOAJ, PubMed, UGC CARE

Publications of NG

Mad-related genes in the human
Bert Vogelstein July, 1996
Resistance to the growth inhibitory effects of TGF-β is common in human cancers1,2. However, the mechanism(s) by which tumour cells become resistant to TGF-β are generally unknown. We have...
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Bert Vogelstein December, 2012
Neuroblastomas are tumors of peripheral sympathetic neurons and are the most common solid tumor in children. To determine the genetic basis for neuroblastoma, we performed whole-genome seque...
Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas
Bert Vogelstein November, 2013
Through exomic sequencing of 32 intrahepatic cholangiocarcinomas, we discovered frequent inactivating mutations in multiple chromatin-remodeling genes (including BAP1, ARID1A and PBRM1), and...
Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis
Bert Vogelstein June, 2001
Juvenile polyposis (JP; OMIM 174900) is an autosomal dominant gastrointestinal hamartomatous polyposis syndrome in which patients are at risk for developing gastrointestinal cancers1,2. Prev...
Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancers
Bert Vogelstein July, 1996
Chromosome deletions are the most common genetic events observed in cancer1–4. These deletions are generally thought to reflect the existence of a tumour suppressor gene within the lost re...
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC
Bert Vogelstein September, 1997
Approximately 130,000 cases of col ore eta I cancer (CRC) are diagnosed in the United States each year1, and about 15% of these have a hereditary component2,3. Two well-defined syndromes, fa...
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability
Bert Vogelstein January, 1995
Microsatellite instability has been observed in both sporadic and hereditary forms of colorectal cancer. In the hereditary form, this instability is generally due to germline mutations in mi...
Analysis of human transcriptomes
Bert Vogelstein December, 1999
How many human genes are expressed ubiquitously, in all human tissues, and how many are expressed in tissue-specific patterns? To answer these fundamental questions in molecular biology, we ...
Deep learning enables genetic analysis of the human thoracic aorta
Emelia J. Benjamin November, 2021
Enlargement or aneurysm of the aorta predisposes to dissection, an important cause of sudden death. We trained a deep learning model to evaluate the dimensions of the ascending and descendin...
Somatic mutations of the mitochondrial genome in human colorectal tumours
Bert Vogelstein November, 1998
Alterations of oxidative phosphorylation in tumour cells were originally believed to have a causative role in cancerous growth1. More recently, mitochondria have again received attention wit...