Author

Kazushiro Tsuji

Observed names: K Tsuji, K. Tsuji, KAZUSHIRO TSUJI, Kazushiro TSUJI

Institution: Okayama University

Observed institutions: Philipps University of Marburg, Okayama University

OpenAlex ID: A5111413410

Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5

1991 · Tatsunori Kobayashi, Kouji Narahara, et al. · American Journal of Medical Genetics · 89

Assignment of human porphobilinogen deaminase to 11q24.1→q24.2 by in situ hybridization and gene dosage studies

2008 · H. Namba, K. Narahara, et al. · Cytogenetics and Cell Genetics · 65

Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: Karyotype‐phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3

1990 · Kouji Narahara, Kiyoshi Kikkawa, et al. · American Journal of Medical Genetics · 60

Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation

1992 · Yuji Yokoyama, Kouji Narahara, et al. · Human Genetics · 45

Growth hormone deficiency and empty sella syndrome in a boy with dup(x)(q13.3→q21.2)

1992 · Yuji Yokoyama, Kouji Narahara, et al. · American Journal of Medical Genetics · 44

Acampomelic campomelic syndrome and sex reversal associated with de novo t(12;17) translocation

1995 · Shinsuke Ninomiya, Kouji Narahara, et al. · American Journal of Medical Genetics · 25

Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and α‐L‐fucosidase 2

1991 · Kouji Narahara, Kazushiro Tsuji, et al. · American Journal of Medical Genetics · 24

Further study on HLA-A, B, C, D, DR and haplotype antigen frequencies in psoriasis vulgaris.

1979 · K Tsuji, H Inouye, et al. · PubMed · 24

Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of malouf syndrome

1992 · Kouji Narahara, Masahiro Kamada, et al. · American Journal of Medical Genetics · 22

Tissue-specific mosaicism for trisomy 21 and congenital heart disease

1992 · Yuji Yokoyama, Kouji Narahara, et al. · The Journal of Pediatrics · 21

Craniosynostosis and hemizygosity for D7S135 caused by a de novo and apparently balanced t(6;7) translocation

1994 · Kazushiro Tsuji, Kouji Narahara, et al. · American Journal of Medical Genetics · 18

Is loss of band 7p21 really critical for manifestation of craniosynostosis in 7p‐?

1993 · Kiyoshi Kikkawa, Kouji Narahara, et al. · American Journal of Medical Genetics · 17

45,X/46,X,idic(Yq) mosaicism: Clinical, cytogenetic, and molecular studies in four individuals

1998 · Michio Teraoka, Koji Narahara, et al. · American Journal of Medical Genetics · 16

Reproductive risk in mating between two translocation carriers: Case report and review of the literature

1993 · Kazushiro Tsuji, Kouji Narahara, et al. · American Journal of Medical Genetics · 14

Cleidocranial dysplasia associated with a t(6;18)(p12;q24) translocation

1995 · Kouji Narahara, Kazushiro Tsuji, et al. · American Journal of Medical Genetics · 13

De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies

1992 · Yoshiharu Wakita, Kouji Narahara, et al. · Human Genetics · 13

Unique karyotypes in two patients with Prader‐Willi syndrome

1992 · Kouji Narahara, Kei Hiramoto, et al. · American Journal of Medical Genetics · 10

The breakpoint on 7p in a patient with t(6;7) and craniosynostosis is spanned by a YAC clone containing the D7S503 locus

1995 · Kazushiro Tsuji, Kouji Narahara, et al. · Human Genetics · 6

Mapping of genes encoding coagulation factors VII and X to the distal portion of the 13q34 by gene dose study in a patient with r(13)

1989 · Ryozo Kasai, Kouji Narahara, et al. · The Japanese Journal of Human Genetics · 6

Rapid screening method to detect mutations inCYP21, the gene for 21-hydroxylase

2000 · Yuji Yokoyama, Michio Teraoka, et al. · American Journal of Medical Genetics · 5

[Urgent mitral valve replacement for acute mitral regurgitation due to ruptured chordae tendineae in systemic lupus erythematousus].

1993 · K Tsuji, K Kino, et al. · PubMed · 3

Developmental change in activity of red cell porphobilinogen deaminase and its electrophoretic variant in the Japanese population

1994 · HIROSHI NAMBA, KOUJI NARAHARA, et al. · Pediatrics International · 1

Chromosome analysis of 632 cases using amniotic fluid cells

1996 · Michio Teraoka, Shoko Mizuta, et al. · Journal of Human Genetics

[Fontan-type procedure for an adult case of double-outlet right ventricle (S, D, L)].

1995 · K Kino, S Sano, et al. · PubMed

Interchange trisomy 9 due to maternal t(6; 9) translocation

1994 · SHINSUKE NINOMIYA, KOUJI NARAHARA, et al. · Pediatrics International

Works count: 31

Citation count: 541

H-index: 14

I10-index: 17