List of works - Kristian Gray

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

scientific article

A review of the new HGNC gene family resource

scientific article

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

scientific article published on 22 May 2005

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

scientific article

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

scientific article published on 7 May 2007

Genenames.org: the HGNC and VGNC resources in 2017

scientific article

Genenames.org: the HGNC and VGNC resources in 2019

Genenames.org: the HGNC resources in 2013

scientific article

Genenames.org: the HGNC resources in 2015

scientific article

Lung cancer: intragenic ERBB2 kinase mutations in tumours

scientific article

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.

scientific article

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor

scientific article

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus

scientific article

Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly

scientific article

Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation

scientific article

Mutations of the BRAF gene in human cancer

scientific article (publication date: 27 June 2002)

RNAcentral: a comprehensive database of non-coding RNA sequences

scientific article (publication date: 4 January 2017)

Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

scientific article

Somatic mutations of the protein kinase gene family in human lung cancer

scientific article published on September 2005

Vive la différence: naming structural variants in the human reference genome ⬇️

scientific article published on May 1, 2013

List of works by Kristian Gray

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

A review of the new HGNC gene family resource

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

Genenames.org: the HGNC and VGNC resources in 2017

Genenames.org: the HGNC and VGNC resources in 2019

Genenames.org: the HGNC resources in 2013

Genenames.org: the HGNC resources in 2015

Lung cancer: intragenic ERBB2 kinase mutations in tumours

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus

Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly

Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation

Mutations of the BRAF gene in human cancer

RNAcentral: a comprehensive database of non-coding RNA sequences

Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

Somatic mutations of the protein kinase gene family in human lung cancer

Vive la différence: naming structural variants in the human reference genome ⬇️