I. Yuasa

发表

Molecular analysis of the human orosomucoid gene ORM1*Q0köln responsible for incompatibility in a German paternity case

L. Henke, J. Henke, E. Nanba, 2000, International Journal of Legal Medicine.

Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers

E. Nanba, K. Takeshita, Takashi Ito, 1996, Brain and Development.

Investigation of Japanese-specific alleles: most are of Jomon lineage.

T. Ishikawa, A. Akane, I. Yuasa, 2015, Legal medicine.

Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific

N. Saitou, L. Henke, J. Henke, 2008, Journal of Human Genetics.

Geographical North-South Decline in DNASE1*2 in Japanese Populations

T. Yasuda, Y. Nakashima, K. Kishi, 2001, Human biology.

MATP polymorphisms in Germans and Japanese: the L374F mutation as a population marker for Caucasoids

I. Yuasa, K. Umetsu, G. Watanabe, 2004, International Journal of Legal Medicine.

Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation

Y. Wada, N. Matsumoto, S. Saitoh, 2015, Clinical genetics.

Serum carbohydrate-deficient transferrin in patients with nonalcoholic liver disease and with hepatocellular carcinoma.

H. Kawasaki, I. Yuasa, Y. Murawaki, 1997, Clinica chimica acta; international journal of clinical chemistry.

The art of traditional native PAGE: The APLP 48-ID assay for human identification.

I. Yuasa, K. Umetsu, M. Hashiyada, 2016, Legal medicine.

Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cyst.

E. Nanba, K. Takeshita, I. Yuasa, 1999, American journal of medical genetics.

A commentary on assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree

I. Yuasa, 2013, Journal of Human Genetics.

Sugar chains of serum transferrin from patients with carbohydrate deficient glycoprotein syndrome. Evidence of asparagine-N-linked oligosaccharide transfer deficiency.

K. Takeshita, I. Yuasa, K. Fukushima, 1993, The Journal of biological chemistry.

Orosomucoid (ORM) typing by isoelectric focusing: evidence for two structural loci ORM1 and ORM2

I. Yuasa, K. Umetsu, M. Robinet-Levy, 1986, Human Genetics.

The rearrangement of the human alpha(1)-acid glycoprotein/orosomucoid gene: evidence for tandemly triplicated genes consisting of two AGP1 and one AGP2.

E. Nanba, H. Nakamura, I. Yuasa, 2000, Biochemical and biophysical research communications.

Association of Functional Gene Polymorphisms of Interleukin-1β and Transforming Growth Factor-β1 with the Progression of Liver Fibrosis in Japanese Patients with Hepatitis C Virus-Related Chronic Liver Disease

I. Yuasa, Y. Murawaki, K. Okamoto, 2007 .

Carbohydrate-deficient glycoprotein syndrome: electrophoretic study of multiple serum glycoproteins

K. Takeshita, I. Yuasa, K. Yamashita, 1995, Brain and Development.

Allele frequencies of a SNP and a 27-bp deletion that are the determinant of earwax type in the ABCC11 gene.

T. Kitano, I. Yuasa, K. Umetsu, 2008, Legal medicine.

Distribution of Alpha-2-HS-glycoprotein. Types in Four East Asian Populations

I. Yuasa, K. Umetsu, M. Ding, 1991 .

Genetic polymorphism of human α2HS‐glycoprotein: Characterization and application to forensic hemogenetics

I. Yuasa, K. Umetsu, 1988 .

On a New Alpha-2-HS-glycoprotein Variant, AHSG 12

I. Yuasa, K. Umetsu, Tsuneo Suzuki, 1988 .

Alpha-2-HS-glycoprotein (A2HS) polymorphism in a Japanese population: Existence of two new variants

I. Yuasa, K. Umetsu, Tsuneo Suzuki, 1987, Japanese Journal of Human Genetics.

The carbohydrate deficient glycoprotein syndrome in three Japanese children

K. Takeshita, I. Yuasa, K. Ohno, 1992, Brain and Development.

Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate‐glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese

K. Hayasaka, K. Akaba, H. Chiba, 1998, Biochemistry and molecular biology international.

The fifth allele of the human deoxyribonuclease I (DNase I) polymorphism

R. Iida, E. Tsubota, M. Aoyama, 1997, Electrophoresis.

A hypervariable STR polymorphism in the CFI gene: southern origin of East Asian-specific group H alleles.

N. Saitou, A. Akane, I. Yuasa, 2013, Legal medicine.

Association of functional gene polymorphisms of matrix metalloproteinase (MMP)‐1, MMP‐3 and MMP‐9 with the progression of chronic liver disease

I. Yuasa, Y. Murawaki, K. Okamoto, 2005, Journal of gastroenterology and hepatology.

Monozygotic twins discordant for Klippel-Feil syndrome.

Y. Maegaki, I. Yuasa, K. Ohno, 2006, Pediatric neurology.

A Decreasing Gradient of 374F Allele Frequencies in the Skin Pigmentation Gene SLC45A2, from the North of West Europe to North Africa

I. Yuasa, G. Lucotte, F. Diéterlen, 2010, Biochemical Genetics.

Characterization of mutants of the vitamin D-binding protein/group-specific component: molecular evolution of GC*1A2 and GC*1A3, common in some Asian populations

A. Braun, I. Yuasa, K. Umetsu, 1995, Human Genetics.

Distribution of Group-Specific Component/Vitamin D-Binding Protein Alleles in Southwestern Japan and Geographical Clines of Allele Frequencies in Japanese Populations

I. Yuasa, K. Ago, O. Tsuganezawa, 1998 .

Gc types in western Japan: report of a new variant Gc 1C35.

I. Yuasa, N. Yokoyama, K. Suenaga, 1984, Human heredity.

Distribution of Hp, Tf, Gc and Pi Polymorphisms in a Japanese Population Sample from San-in District

I. Yuasa, Y. Saneshige, N. Okamoto, 1983 .

Distribution of Hp, Tf, Gc and Pi polymorphisms in a Nepalese population.

I. Yuasa, J. Ikebuchi, T. Hikita, 1983, Human heredity.

Distinct C‐terminus of the B subunit of factor XIII in a population‐associated major phenotype: the first case of complete allele‐specific alternative splicing products in the coagulation and fibrinolytic systems

H. Iwata, T. Kitano, I. Yuasa, 2009, Journal of thrombosis and haemostasis : JTH.

ITIH1* Q0iwate, a null allele of inter-alpha-trypsin inhibitor H1 caused by deletion/frameshift mutation

I. Yuasa, K. Umetsu, Y. Aoki, 1997, Japanese Journal of Human Genetics.

Parentally imprinted allele typing at a short tandem repeat locus in intron 1a of imprinted gene KCNQ1.

I. Yuasa, H. Yamanouchi, K. Dewa, 2006, Legal medicine.

The global distribution of the p.R1193Q polymorphism in the SCN5A gene.

K. Hara, I. Yuasa, K. Umetsu, 2016, Legal medicine.

Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia

I. Yuasa, K. Yamashita, K. Ohno, 2003, Brain & development (Tokyo. 1979).

Orosomucoid typing of apes (family Pongidae) by isoelectric focusing: Among primates do only humans have two functional orosomucoid loci?

Y. Kawamoto, O. Takenaka, I. Yuasa, 1991, Biochemical Genetics.

Orosomucoid typing of apes (family Pongidae) by isoelectric focusing: Among primates do only humans have two functional orosomucoid loci?

Y. Kawamoto, O. Takenaka, I. Yuasa, 1991, Biochemical Genetics.

Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*S

E. Nanba, I. Yuasa, K. Umetsu, 1997, Human Genetics.

Orosomucoid Phenotyping Using Monoclonal Antibodies

I. Yuasa, K. Umetsu, T. Suzuki, 1994 .

Orosomucoid System: 17 Additional Orosomucoid Variants and Proposal for a New Nomenclature

P. Baumann, I. Yuasa, K. Umetsu, 1993, Vox sanguinis.

Orosomucoid (ORM) Typing by Isoelectric Focusing: Evidence for Several New Variants Including ORM1 and ORM2 Silent Alleles

I. Yuasa, K. Umetsu, Tsuneo Suzuki, 1990, Vox sanguinis.

Orosomucoid typing by isoelectric focusing: Genetic variation of orosomucoid in Asian macaques (genus Macaca)

T. Ishida, K. Terao, Y. Kawamoto, 1990, Electrophoresis.

Y-chromosomal STR haplotyping in a Japanese population.

I. Yuasa, K. Umetsu, K. Ago, 2000, Legal medicine.

OCA2*481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations

N. Saitou, L. Henke, J. Henke, 2007, Journal of Human Genetics.

PI*Siiyama, a deficiency gene of alpha1-antitrypsin: Evidence for the occurrence in western Japan

Y. Fukumaki, I. Yuasa, Takao Sasaki, 1993, Japanese Journal of Human Genetics.

Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations.

N. Saitou, I. Yuasa, K. Umetsu, 2011, Legal medicine.

Alpha 1‐antitrypsin and orosomucoid phenotyping using allo A lectin‐peroxidase for detection

K. Taketa, I. Yuasa, K. Umetsu, 1987 .

Nonsynonymous single-nucleotide polymorphisms of the human apoptosis-related endonuclease--DNA fragmentation factor beta polypeptide, endonuclease G, and Flap endonuclease-1--genes show a low degree of genetic heterogeneity.

R. Iida, T. Yasuda, Y. Koda, 2012, DNA and cell biology.

Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass Spectrometry.

R. Wierenga, A. Haapalainen, T. Fukao, 2012, JIMD reports.

Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis

E. Nanba, Y. Maegaki, M. Sasaki, 2017, Brain and Development.

Molecular characterization of four alpha-1-antitrypsin variant alleles found in a Japanese population: a mutation hot spot at the codon for amino acid 362.

I. Yuasa, K. Umetsu, K. Ago, 2001, Legal medicine.

A new α1-antitrypsin allele PI*Poki: Isoelectric focusing with immobilized pH gradients as a tool for identification of PI variants

I. Yuasa, K. Okada, 2004, Human Genetics.

Genetic polymorphism of alpha-2-HS-glycoprotein: four new alleles and allele frequencies in Japanese.

S. Kashimura, I. Yuasa, K. Umetsu, 1991, Human heredity.

Genetic variants associated with arsenic metabolism within human arsenic (+3 oxidation state) methyltransferase show wide variation across multiple populations

T. Yasuda, A. Panduro, I. Yuasa, 2011, Archives of Toxicology.

Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder‐Haplotype Analysis

N. Saitou, L. Henke, J. Henke, 2006, Annals of human genetics.

Distribution of Two Asian-Related Coding SNPs in the MC1R and OCA2 Genes

N. Saitou, L. Henke, J. Henke, 2007, Biochemical Genetics.

Transferrin variants in Japan and New Zealand. Report of an unusually sialyzed TF variant.

I. Yuasa, K. Suenaga, Y. Gotoh, 1987, Human heredity.

Orosomucoid (ORM) typing by isoelectric focusing: description of two new alleles in a German population and thermostability in bloodstains

I. Yuasa, K. Umetsu, B. Brinkmann, 1989, Zeitschrift für Rechtsmedizin.

Orosomucoid (ORM) typing by isoelectric focusing: evidence for gene duplication of ORM1 and genetic polymorphism of ORM2

I. Yuasa, K. Umetsu, M. Robinet-Levy, 1987, Human Genetics.

Increased expression of β-hexosaminidase α chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I

Yoshiyuki Suzuki, E. Nanba, H. Sakuraba, 1998, Brain & development (Tokyo. 1979).

Increased expression of beta-hexosaminidase alpha chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I.

E. Nanba, Y. Suzuki, H. Sakuraba, 1998, Brain & development.

Transferrin Polymorphism in the Nansei Islands: Description of a New Variant TF Dama and Clines of Allele Frequencies in Japanese Populations

I. Yuasa, K. Ago, O. Tsuganezawa, 1998 .

Origin and evolution of gene for prolactin-induced protein.

N. Saitou, W. Tian, T. Kitano, 2006, Gene.

De Novo Mutations in SLC35A2 Encoding a UDP‐Galactose Transporter Cause Early‐Onset Epileptic Encephalopathy

Y. Wada, N. Matsumoto, Y. Maegaki, 2013, Human mutation.

Simple and rapid determination of the acetaldehyde dehydrogenase (ALDH2) genotypes by nonradioactive single‐strand conformation polymorphism analysis

I. Yuasa, K. Umetsu, M. Nakagawa, 1997, Electrophoresis.

Genotyping of the ABO blood group system: analysis of nucleotide position 802 by PCR-RFLP and the distribution of ABO genotypes in a German population

I. Yuasa, H. Nishimukai, Y. Fukumori, 2005, International Journal of Legal Medicine.

Amplified product length polymorphism (APLP): a novel strategy for genotyping the ABO blood group

I. Yuasa, K. Umetsu, T. Suzuki, 1996, Human Genetics.

Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution.

R. Iida, T. Yasuda, I. Yuasa, 2012, Legal medicine.

Confirmation that SNPs in the high mobility group‐A2 gene (HMGA2) are associated with adult height in the Japanese population; wide‐ranging population survey of height‐related SNPs in HMGA2

R. Iida, T. Yasuda, Y. Koda, 2011, Electrophoresis.

HERC1 polymorphisms: population‐specific variations in haplotype composition

N. Saitou, L. Henke, J. Henke, 2009, Cell biochemistry and function.

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I

Machiko Kadoya, Y. Wada, R. Wevers, 2011, Journal of Inherited Metabolic Disease.

Forensic species identification based on size variation of mitochondrial DNA hypervariable regions

I. Yuasa, Hiroaki Nakamura, S. Imamura, 2009, International Journal of Legal Medicine.

The Human Complement Component C1R Gene: The Exon‐intron Structure and the Molecular Basis of Allelic Diversity

I. Yuasa, K. Umetsu, M. Nakagawa, 2003, Annals of human genetics.

DXS10011: a hypervariable tetranucleotide STR polymorphism on the X chromosome

I. Yuasa, K. Umetsu, T. Suzuki, 2000, International Journal of Legal Medicine.

Nucleotide substitution in the 5' flanking region of D1S80 locus.

I. Yuasa, K. Umetsu, T. Suzuki, 1997, Forensic science international.

A new single-nucleotide polymorphism in the seventh component of complement (C7) gene

I. Yuasa, K. Umetsu, M. Nakagawa, 1999, Journal of Human Genetics.

A Japanese-specific allele in the GALNT11 gene.

N. Saitou, L. Henke, J. Henke, 2010, Legal medicine.

Simultaneous determination of seven informative Y chromosome SNPs to differentiate East Asian, European, and African populations.

R. Iida, T. Yasuda, I. Yuasa, 2011, Legal medicine.

Allele frequencies and haplotypes for 28 Y-STRs in Ovambo population.

R. Iida, E. Tsubota, T. Yasuda, 2009, Legal medicine.

Near Fixation of 374l Allele Frequencies of the Skin Pigmentation Gene SLC45A2 in Africa

I. Yuasa, G. Lucotte, 2013, Biochemical Genetics.

More genetic studies on the inference of ancestry and morphological traits: response from the authors to the letter from Salas et al.

I. Yuasa, K. Umetsu, 2006, International Journal of Legal Medicine.

Extreme mtDNA homogeneity in continental Asian populations.

M. Stoneking, N. Saitou, T. Kitano, 2002, American journal of physical anthropology.

Mutation in the exon 10 (R173W) of the hydroxymethylbilane synthase gene in two unrelated Japanese families with acute intermittent porphyria.

E. Nanba, I. Yuasa, F. Tajima, 1998, Research communications in molecular pathology and pharmacology.

The genotypes of IL-1 beta and MMP-3 are associated with the prognosis of HCV-related hepatocellular carcinoma.

I. Yuasa, Y. Murawaki, Y. Ikebuchi, 2010, Internal medicine.

PI (α1) polymorphism in the Japanese: Confirmation of PI*M4 and description of new PI variants

I. Yuasa, N. Yokoyama, K. Suenaga, 2004, Human Genetics.

PI Mtoyoura: A new PI M subtype found by separator and hybrid isoelectric focusing

I. Yuasa, K. Umetsu, K. Okada, 1988, Electrophoresis.

A hypervariable STR polymorphism in the CFI gene: mutation rate and no linkage disequilibrium with FGA.

I. Yuasa, K. Umetsu, K. Dewa, 2013, Legal medicine.

Molecular Basis of ESD*5 and ESD*7 and Haplotype Analysis with New Polymorphisms in Introns

L. Henke, J. Henke, I. Yuasa, 2004, Human biology.

Population Genetic Studies on Nine Aboriginal Ethnic Groups of Taiwan II. Serum Protein Systems

N. Saitou, S. Horai, T. Ishida, 2001 .

Orosomucoid phenotyping with monoclonal antibodies:polymorphic occurrence of ORM1*Q0 in aboriginal Taiwanese populations.

N. Saitou, S. Horai, T. Ishida, 1995, Human heredity.

Polymorphisms of complement component I and C1R subcomponent of C1 in nine aboriginal Taiwanese populations.

N. Saitou, S. Horai, T. Ishida, 1994, Human biology.

Reliable phenotyping of esterase D by low voltage isoelectric focusing: Evidence for the new variant ESD Yamaguchi

I. Yuasa, K. Ito, Terutaka Inoue, 1985 .

Genotyping of the c.1423C>T (p.P475S) polymorphism in the ADAMTS13 gene by APLP and HRM assays: Northeastern Asian origin of the mutant.

M. Iino, T. Ishikawa, I. Yuasa, 2016, Legal medicine.

A hypervariable STR polymorphism in the complement factor I (CFI) gene: Asian-specific alleles

N. Saitou, L. Henke, J. Henke, 2009, International Journal of Legal Medicine.

Multiplex amplified product‐length polymorphism analysis of 36 mitochondrial single‐nucleotide polymorphisms for haplogrouping of East Asian populations

S. Kashimura, Yau-Huei Wei, I. Yuasa, 2005, Electrophoresis.

Determination of α2HS-glycoprotein phenotypes by isoelectric focusing and immunoblotting: polymorphic occurrence of HSGA*5 in Okinawa

I. Yuasa, T. Taira, K. Suenaga, 2004, Human Genetics.

Factor I (C3b inactivator) polymorphism among five populations in Eurasia.

I. Yuasa, K. Umetsu, M. Robinet-Levy, 1988, Human heredity.

Multiplex amplified product‐length polymorphism analysis for rapid detection of human mitochondrial DNA variations

N. Saitou, S. Kashimura, N. Fuku, 2001, Electrophoresis.

Haplotype analysis of the human α2‐HS glycoprotein (fetuin) gene

N. Saitou, T. Kitano, J. Henke, 2001, Annals of human genetics.

Simultaneous genotyping of alcohol dehydrogenase 2 (ADH2) and aldehyde dehydrogenase 2 (ALDH2) loci by amplified product length polymorphism (APLP) analysis

I. Yuasa, K. Umetsu, Tsuneo Suzuki, 1998, Electrophoresis.

Recent progress in mitochondrial DNA analysis.

I. Yuasa, K. Umetsu, 2005, Legal medicine.

Simultaneous genotyping of 11 non-synonymous SNPs in the 4 glutathione peroxidase genes using the multiplex single base extension method.

R. Iida, E. Tsubota, T. Yasuda, 2009, Clinica chimica acta; international journal of clinical chemistry.

Orosomucoid (ORM) typing by isoelectric focusing: evidence for an additional duplicated ORM1 locus haplotype and close linkage of two ORM loci.

I. Yuasa, K. Umetsu, K. Suenaga, 1988, American journal of human genetics.

Orosomucoid (ORM) typing by isoelectric focusing: an analysis of ORM haplotypes.

I. Yuasa, K. Umetsu, J. Ikebuchi, 1990, Human heredity.

Genetic polymorphisms of orosomucoid and alpha-2-HS-glycoprotein in a Philippine population.

I. Yuasa, K. Umetsu, T. Suzuki, 1988, Human heredity.

Genetic polymorphisms of orosomucoid and alpha-2-HS-glycoprotein in Thai, Sri Lankan and Paraguayan populations

T. Ishida, I. Yuasa, K. Umetsu, 1989, Japanese Journal of Human Genetics.

The Structure and Diversity of α1-Acid Glycoprotein/Orosomucoid Gene in Africans

L. Henke, J. Henke, I. Yuasa, 2006, Biochemical Genetics.

Characterization of genomic rearrangements of the α1-acid glycoprotein/orosomucoid gene in Ghanaians

L. Henke, J. Henke, I. Yuasa, 2001, Journal of Human Genetics.

Genetic polymorphisms of orosomucoid ORM1 and ORM2 in Egyptians, Sudanese, and Qataris: occurrence of two new alleles.

I. Yuasa, J. Tie, S. Oshida, 1997, Human Biology: The Official Publication of the American Association of Anthropological Genetics.

Detection of orosomucoid 1 phenotypes in semen and semen stains.

I. Yuasa, K. Umetsu, T. Suzuki, 1989, Journal of forensic sciences.

Orosomucoid 1 and orosomucoid 2 types in the Taiwanese and Japanese: Evidence for five new orosomucoid variants

I. Yuasa, K. Umetsu, E. Chen, 1988, Electrophoresis.

Genetic Polymorphism of α2HS-Glycoprotein in a French Population

I. Yuasa, K. Umetsu, J. Ikebuchi, 1988 .

Genetic polymorphism of alpha 2HS-glycoprotein in a French population. Description of two new rare variants.

I. Yuasa, K. Umetsu, J. Ikebuchi, 1988, Human heredity.

Genetic variation of alpha-2-HS-glycoprotein in the Kyushu district of Japan: description of three new rare variants.

S. Kashimura, I. Yuasa, K. Umetsu, 1990, Human heredity.

Isoelectric focusing studies in Brazilian Indians —uncovering variation of ORM, AHSG and IF—

F. Salzano, F. Black, I. Yuasa, 1990, Japanese Journal of Human Genetics.

A2HS*11: A new allele of alpha‐2‐HS‐glycoprotein found in Afro‐Caribbeans

I. Yuasa, K. Umetsu, S. Weidinger, 1987 .

Comparative Typing of Orosomucoid Variants and Proposal for a New Nomenclature

I. Yuasa, K. Umetsu, S. Weidinger, 1992 .

Orosomucoid 1 phenotyping from human urine by isoelectric focusing.

I. Yuasa, K. Umetsu, T. Suzuki, 1990, Journal of forensic sciences.

Population genetics of 17 Y-chromosomal STR loci in Japanese.

S. Kashimura, A. Tamura, Koichi Suzuki, 2008, Forensic science international. Genetics.

Molecular aspects of biochemical markers.

I. Yuasa, K. Umetsu, Isao Yuasa, 2005, Legal medicine.

Intragenic haplotypes and molecular evolution of the human α2-HS glycoprotein (AHSG/fetuin) gene

J. Henke, M. Kaneko, I. Yuasa, 2003 .

Haplotype analysis of the human alpha2-HS glycoprotein (fetuin) gene.

N. Saitou, T. Kitano, J. Henke, 2001, Annals of human genetics.

Variation of interleukin 8 -251 A>T polymorphism in worldwide populations and intra-ethnic differences in Japanese populations.

R. Iida, T. Yasuda, K. Shiwaku, 2007, Clinica chimica acta; international journal of clinical chemistry.

Novel paternity testing by distinguishing parental alleles at a VNTR locus in the differentially methylated region upstream of the human H19 gene.

I. Yuasa, K. Umetsu, H. Yamanouchi, 2003, Journal of forensic sciences.

Global genetic analysis of all single nucleotide polymorphisms in exons of the human deoxyribonuclease I‐like 3 gene and their effect on its catalytic activity

R. Iida, T. Yasuda, I. Yuasa, 2011, Electrophoresis.

Genetic and expression analysis of all non‐synonymous single nucleotide polymorphisms in the human deoxyribonuclease I‐like 1 and 2 genes

R. Iida, T. Yasuda, I. Yuasa, 2010, Electrophoresis.

Genetic and expression analysis of all 7 non-synonymous single nucleotide polymorphisms in the human deoxyribonuclease II gene, with potential relevance to autoimmunity.

R. Iida, T. Yasuda, I. Yuasa, 2010, Clinica chimica acta; international journal of clinical chemistry.

Caucasian-specific allele in non-synonymous single nucleotide polymorphisms of the gene encoding deoxyribonuclease I-like 3, potentially relevant to autoimmunity, produces an inactive enzyme.

R. Iida, T. Yasuda, A. Panduro, 2009, Clinica chimica acta; international journal of clinical chemistry.

Incontinentia pigmenti in identical twins with separate skin and neurological disorders.

K. Tanaka, I. Yuasa, S. Takashima, 1990, Acta dermato-venereologica.

Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I‐like 1 and 2 genes

R. Iida, T. Yasuda, Y. Koda, 2010, Electrophoresis.

Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate‐deficient glycoprotein syndrome type 1

K. Shigemoto, Y. Kuroda, I. Kondo, 1999, Clinical genetics.

Development of Genotyping Methods for Single Nucleotide Polymorphism in the Human Pancreatic Ribonuclease Gene (RNASE1) and Their Application to Population Studies

R. Iida, T. Yasuda, I. Yuasa, 2008, Biochemical Genetics.

Simultaneous determination of STR polymorphism and a new nucleotide substitution in its flanking region at the CD4 locus.

T Suzuki, K Umetsu, I. Yuasa, 1998, Journal of forensic sciences.

Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I

K. Shigemoto, I. Kondo, I. Yuasa, 1999, Brain and Development.

A novel dimorphism in the human SRY gene: usefulness in human migration studies

I. Yuasa, K. Umetsu, H. Yamanouchi, 2001, International Journal of Legal Medicine.

Haplotype analysis of seven Y-STRs (eleven loci) in two Japanese populations.

I. Yuasa, K. Umetsu, Hiroaki Nakamura, 2008, Legal medicine.

Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion.

Y. Wada, H. Kurahashi, I. Yuasa, 2019, JIMD reports.

Hemostatic studies in patients with carbohydrate-deficient glycoprotein syndrome.

K. Takeshita, I. Yuasa, K. Ohno, 1994, Thrombosis research.

Japaneseplex: A forensic SNP assay for identification of Japanese people using Japanese-specific alleles.

M. Iino, T. Ishikawa, A. Akane, 2018, Legal medicine.

Distribution of MN genotypes detected by PCR-SSCP analysis

I. Yuasa, Y. Aoki, M. Hashiyada, 2003 .

Determination of carbohydrate‐deficient transferrin separated by lectin affinity chromatography for detecting chronic alcohol abuse

I. Yuasa, K. Umetsu, K. Yamashita, 1999, FEBS letters.

Cutis laxa with frontoparietal cortical malformation: a novel type of congenital disorder of glycosylation.

T. Okanishi, Y. Maegaki, I. Yuasa, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The association of MMP-1, -3 and -9 genotypes with the prognosis of HCV-related hepatocellular carcinoma patients.

I. Yuasa, Y. Murawaki, K. Okamoto, 2005, Research communications in molecular pathology and pharmacology.

De Novo Mutations in SLC35A2 Encoding a UDP‐Galactose Transporter Cause Early‐Onset Epileptic Encephalopathy

Y. Wada, N. Matsumoto, Y. Maegaki, 2013, Human mutation.

Intragenic haplotypes and molecular evolution of the human a 2-HS glycoprotein ( fetuin ) gene

J. Henke, M. Kaneko, I. Yuasa, 2003 .