Publications:

---

Gene-wide significant association analyses of DNMT1 genetic variants with Parkinson's disease.

Frontiers In Genetics

Wang, Jian-Yong JY; Cui, Lei L; Shi, Hong-Yi HY; Chen, Ling-Hao LH; Jin, Ren-Wei RW; Jiang, Xiao-Xia XX; Chen, Zhu-Ling ZL; Zhu, Jian-Hong JH; Zhang, Xiong X

Publication Date: 2023

Variant appearance in text: rs759920

PubMed Link: 36950137

Variant Present in the following documents:

• Main text
• fgene-14-1112388.pdf

View BVdb publication page

---

Hearing loss and brain disorders: A review of multiple pathologies.

Open Medicine (Warsaw, Poland)

Oluwole, Oluwafemi Gabriel OG; James, Kili K; Yalcouye, Abdoulaye A; Wonkam, Ambroise A

Publication Date: 2022

Variant appearance in text: rs759920

PubMed Link: 34993346

Variant Present in the following documents:

• Main text
• med-2021-0402.pdf

View BVdb publication page

---

Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: DNMT1: 649-197T>C; rs759920

PubMed Link: 30319441

Variant Present in the following documents:

• Table_6.xlsx, sheet 1
• Table_5.xlsx, sheet 1

View BVdb publication page

---

Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival.

International Journal Of Cancer

Li, Bo B; Wang, Yanru Y; Xu, Yinghui Y; Liu, Hongliang H; Bloomer, Wendy W; Zhu, Dakai D; Amos, Christopher I CI; Fang, Shenying S; Lee, Jeffrey E JE; Li, Xin X; Han, Jiali J; Wei, Qingyi Q

Publication Date: 2018-06-01

Variant appearance in text: rs759920

PubMed Link: 29313974

Variant Present in the following documents:

• Main text

View BVdb publication page

---

Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs759920

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

---

DNA methyl transferase (DNMT) gene polymorphisms could be a primary event in epigenetic susceptibility to schizophrenia.

Plos One

Saradalekshmi, Koramannil Radha KR; Neetha, Nanoth Vellichiramal NV; Sathyan, Sanish S; Nair, Indu V IV; Nair, Chandrasekharan M CM; Banerjee, Moinak M

Publication Date: 2014

Variant appearance in text: rs759920

PubMed Link: 24859147

Variant Present in the following documents:

• Main text
• pone.0098182.pdf

View BVdb publication page

---

Cocoa Consumption Alters the Global DNA Methylation of Peripheral Leukocytes in Humans with Cardiovascular Disease Risk Factors: A Randomized Controlled Trial.

Plos One

Crescenti, Anna A; Solà, Rosa R; Valls, Rosa M RM; Caimari, Antoni A; Del Bas, Josep M JM; Anguera, Anna A; Anglés, Neus N; Arola, Lluís L

Publication Date: 2013

Variant appearance in text: rs759920

PubMed Link: 23840361

Variant Present in the following documents:

• Main text

View BVdb publication page

---

DNMT1, DNMT3A and DNMT3B gene variants in relation to ovarian cancer risk in the Polish population.

Molecular Biology Reports

Mostowska, Adrianna A; Sajdak, Stefan S; Pawlik, Piotr P; Lianeri, Margarita M; Jagodzinski, Paweł P PP

Publication Date: 2013-08

Variant appearance in text: rs759920

PubMed Link: 23666104

Variant Present in the following documents:

• Main text
• 11033_2013_Article_2589.pdf

View BVdb publication page

---