List of works - Sergey Batalov

A Comparison of the Celera and Ensembl Predicted Gene Sets Reveals Little Overlap in Novel Genes

article

A coactivator trap identifies NONO (p54nrb) as a component of the cAMP-signaling pathway

scholarly article

A conserved salt bridge in the G loop of multiple protein kinases is important for catalysis and for in vivo Lyn function.

scientific article published in January 2009

An approach to genomewide screens of expressed small interfering RNAs in mammalian cells.

scientific article published on 19 December 2003

Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

scientific article (publication date: 5 December 2002)

Analysis of the mouse transcriptome for genes involved in the function of the nervous system.

scientific article

Concomitant diagnosis of immune deficiency and sepsis in a 19 month old with ecthyma gangrenosum by host whole-genome sequencing

scientific article published on 17 December 2018

Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation

scientific article published on 01 April 2019

Discovery of gene function by expression profiling of the malaria parasite life cycle

scientific article (publication date: 12 September 2003)

Do aligned sequences share the same fold?

scientific article published on 01 October 1997

Excess Polymorphisms in Genes for Membrane Proteins in Plasmodium falciparum

scientific article published in Science

Fitness costs of rifampicin resistance in Mycobacterium tuberculosis are amplified under conditions of nutrient starvation and compensated by mutation in the β' subunit of RNA polymerase

scientific article published on 26 February 2014

Functional annotation of a full-length mouse cDNA collection

scientific article (publication date: 8 February 2001)

Genome-wide functional analysis of human cell-cycle regulators.

scientific article published on 25 September 2006

High throughput mutagenesis for identification of residues regulating human prostacyclin (hIP) receptor expression and function

scientific article (publication date: 2014)

Identification of Modulators of TRAIL-Induced Apoptosis via RNAi-Based Phenotypic Screening ⬇️

scientific article published on September 1, 2003

Identification of synthetic lethality of PRKDC in MYC-dependent human cancers by pooled shRNA screening.

scientific article

Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses

scientific article published on 11 August 2020

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

scientific article published on 22 April 2021

Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome.

scientific article published on September 2017

Rapid whole-genome sequencing identifies a novel homozygous NPC1 variant associated with Niemann-Pick type C1 disease in a 7-week-old male with cholestasis.

scientific article published on 26 May 2017

Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease

article

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.

scientific article published on 9 February 2018

The transcriptional landscape of the mammalian genome

scientific article

Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAs

scientific article published in April 2006

Ubiquitin-mediated sequestration of normal cellular proteins into polyglutamine aggregates

scientific article

Whole-genome sequencing and microarray analysis of ex vivo Plasmodium vivax reveal selective pressure on putative drug resistance genes

scientific article

List of works by Sergey Batalov

A Comparison of the Celera and Ensembl Predicted Gene Sets Reveals Little Overlap in Novel Genes

A coactivator trap identifies NONO (p54nrb) as a component of the cAMP-signaling pathway

A conserved salt bridge in the G loop of multiple protein kinases is important for catalysis and for in vivo Lyn function.

An approach to genomewide screens of expressed small interfering RNAs in mammalian cells.

Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

Analysis of the mouse transcriptome for genes involved in the function of the nervous system.

Concomitant diagnosis of immune deficiency and sepsis in a 19 month old with ecthyma gangrenosum by host whole-genome sequencing

Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation

Discovery of gene function by expression profiling of the malaria parasite life cycle

Do aligned sequences share the same fold?

Excess Polymorphisms in Genes for Membrane Proteins in Plasmodium falciparum

Fitness costs of rifampicin resistance in Mycobacterium tuberculosis are amplified under conditions of nutrient starvation and compensated by mutation in the β' subunit of RNA polymerase

Functional annotation of a full-length mouse cDNA collection

Genome-wide functional analysis of human cell-cycle regulators.

High throughput mutagenesis for identification of residues regulating human prostacyclin (hIP) receptor expression and function

Identification of Modulators of TRAIL-Induced Apoptosis via RNAi-Based Phenotypic Screening ⬇️

Identification of synthetic lethality of PRKDC in MYC-dependent human cancers by pooled shRNA screening.

Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome.

Rapid whole-genome sequencing identifies a novel homozygous NPC1 variant associated with Niemann-Pick type C1 disease in a 7-week-old male with cholestasis.

Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.

The transcriptional landscape of the mammalian genome

Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAs

Ubiquitin-mediated sequestration of normal cellular proteins into polyglutamine aggregates

Whole-genome sequencing and microarray analysis of ex vivo Plasmodium vivax reveal selective pressure on putative drug resistance genes