Genomics Journal

Overview

publication venue for

• An informatics approach to distinguish RNA modifications in nanopore direct RNA sequencing..  114. 2022
• Betacoronavirus-specific alternate splicing..  114. 2022
• Genetic variants of resistin and its plasma levels: Association with obesity and dyslipidemia related to type 2 diabetes susceptibility..  111. 2018
• One in four individuals of African-American ancestry harbors a 5.5kb deletion at chromosome 11q13.1..  103. 2014
• Gene expression analysis uncovers novel hedgehog interacting protein (HHIP) effects in human bronchial epithelial cells..  101. 2013
• Conservation and regulatory associations of a wide affinity range of mouse transcription factor binding sites..  95. 2010
• Discovery of 342 putative new genes from the analysis of 5'-end-sequenced full-length-enriched cDNA human transcripts..  85. 2005
• A 700-kb physical and transcription map of the cervical cancer tumor suppressor gene locus on chromosome 11q13..  85. 2005
• The human HERC family of ubiquitin ligases: novel members, genomic organization, expression profiling, and evolutionary aspects..  85. 2005
• Identification and characterization of mouse SSX genes: a multigene family on the X chromosome with restricted cancer/testis expression..  82. 2003
• Chromosomal distribution of the human cardiovascular transcriptome..  81. 2003
• Radiation hybrid map, physical map, and low-pass genomic sequence of the canine prcd region on CFA9 and comparative mapping with the syntenic region on human chromosome 17..  81. 2003
• Insertional mutagenesis of the mouse acid ceramidase gene leads to early embryonic lethality in homozygotes and progressive lipid storage disease in heterozygotes..  79. 2002
• Low mutational burden of individual acquired mitochondrial DNA mutations in brain..  73. 2001
• Cloning and characterization of a Golgin-related gene from the large-scale polymorphism linked to the PML gene..  70. 2000
• Human BAC ends quality assessment and sequence analyses..  63. 2000
• The human cystathionine beta-synthase (CBS) gene: complete sequence, alternative splicing, and polymorphisms..  52. 1998
• Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome..  48. 1998
• Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21..  46. 1997
• Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigens..  45. 1997
• Cloning and mapping of the MEIS1 gene, the human homolog of a murine leukemogenic gene..  43. 1997
• Localization of the Rab escort protein-2 (REP2) and inositol 1,4,5-trisphosphate 3-kinase (ITPKB) genes to mouse chromosome 1 by in situ hybridization and precision of the syntenic regions between mouse and human 1q42-q44..  43. 1997
• NEUROD2 and NEUROD3 genes map to human chromosomes 17q12 and 5q23-q31 and mouse chromosomes 11 and 13, respectively..  40. 1997
• Astrotactin (ASTN), a gene for glial-guided neuronal migration, maps to human chromosome 1q25.2..  40. 1997
• The human GATA-6 gene: structure, chromosomal location, and regulation of expression by tissue-specific and mitogen-responsive signals..  38. 1996
• Physical mapping of a commonly deleted region, the site of a candidate tumor suppressor gene, at 12q22 in human male germ cell tumors..  35. 1996
• Polymorphism in and localization of the gene LCP2 (SLP-76) to chromosome 5q33.1-qter..  35. 1996
• The NEUROD gene maps to human chromosome 2q32 and mouse chromosome 2..  34. 1996
• Assignment of human myocyte-specific enhancer binding factor 2C (hMEF2C) to human chromosome 5q14 and evidence that MEF2C is evolutionarily conserved..  29. 1995
• Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reaction..  29. 1995
• A locus for cerebral cavernous malformations maps to chromosome 7q in two families..  28. 1995
• The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphism..  26. 1995
• The structure of the human sterol carrier protein X/sterol carrier protein 2 gene (SCP2)..  24. 1994
• Mouse cellular nucleic acid binding proteins: a highly conserved family identified by genetic mapping and sequencing..  24. 1994
• Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL1 maps to human chromosome 1q21, a region that is frequently altered in preneoplastic and neoplastic disease..  23. 1994
• Assignment of the human pancreatic regenerating (REG) gene to chromosome 2p12..  20. 1994
• Localization of the gene (OGDH) coding for the E1k component of the alpha-ketoglutarate dehydrogenase complex to chromosome 7p13-p11.2..  20. 1994
• 3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21..  19. 1994
• Human myosin-binding protein H (MyBP-H): complete primary sequence, genomic organization, and chromosomal localization..  16. 1993
• Fanconi anemia: evidence for linkage heterogeneity on chromosome 20q..  9. 1991
• Somatic cell genetic analysis of human cell surface antigens 5.1H11 and F35/9 (gp45)..  6. 1990

Identity

ISO Abbreviation

• Genomics

Linking ISSN

• 0888-7543

International Standard Serial Number (ISSN)

• 0888-7543

Electronic International Standard Serial Number (EISSN)

• 1089-8646