Satoshi Suzuki
Nagoya, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Evaluating the Role of VAX1, MAFB, and NOG in Non-Syndromic Cleft Palate Only Among Japanese Individuals.
Journal: Congenital anomalies
Published: April 13, 2026
The Suggestive Association Between the NOG rs227731 Polymorphism and Non-Syndromic Cleft Lip With or Without Palate Subtypes in a Japanese Cohort.
Journal: Congenital anomalies
Published: July 24, 2025
Family based and case-control designs reveal an association of TFAP2A in nonsyndromic cleft lip only among Vietnamese population.
Journal: Molecular genetics & genomic medicine
Published: April 26, 2021
SPECC1L regulates palate development downstream of IRF6.
Journal: Human molecular genetics
Published: April 23, 2019
Patients with SATB2-associated syndrome exhibiting multiple odontomas.
Journal: American journal of medical genetics. Part A
Published: July 30, 2018
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
Journal: Genetic epidemiology
Published: June 14, 2017
Association of MEOX2 polymorphism with nonsyndromic cleft palate only in a Vietnamese population.
Journal: Congenital anomalies
Published: June 13, 2017
Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.
Journal: American journal of medical genetics. Part A
Published: July 10, 2014
Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
Journal: American journal of medical genetics. Part A
Published: June 11, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026