Keiichiro Joh

An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease.

Journal: Annals of human genetics

Published: February 18, 2021

Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.

Journal: Clinical epigenetics

Published: September 12, 2018

Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.

Journal: Epigenetics & chromatin

Published: March 09, 2018

An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression.

Journal: PloS one

Published: November 09, 2016

The allele frequency of ALDH2Glu504Lys and ADH1BArg47His for the Ryukyu islanders and their history of expansion among East Asians.

Journal: American journal of human biology : the official journal of the Human Biology Council

Published: June 23, 2016

Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.

Journal: Human molecular genetics

Published: December 28, 2015

The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.

Journal: Gene

Published: September 01, 2015

Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.

Journal: Clinical genetics

Published: July 08, 2014

Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 10, 2013

A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.

Journal: Clinical genetics

Published: August 05, 2013

Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma.

Journal: BMC cancer

Published: March 13, 2013

Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.

Journal: European journal of human genetics : EJHG

Published: November 02, 2012

An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease.

An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease.

Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.

Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.

Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.

Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.

An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression.

An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression.

The allele frequency of ALDH2*Glu504Lys and ADH1B*Arg47His for the Ryukyu islanders and their history of expansion among East Asians.

The allele frequency of ALDH2*Glu504Lys and ADH1B*Arg47His for the Ryukyu islanders and their history of expansion among East Asians.

Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.

Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.

The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.

The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.

Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.

Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.

Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations.

Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations.

A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.

A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.

Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma.

Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma.

Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.

Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.

The allele frequency of ALDH2Glu504Lys and ADH1BArg47His for the Ryukyu islanders and their history of expansion among East Asians.

The allele frequency of ALDH2Glu504Lys and ADH1BArg47His for the Ryukyu islanders and their history of expansion among East Asians.