Publications:

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Response prediction in patients with gastric and esophagogastric adenocarcinoma under neoadjuvant chemotherapy using targeted gene expression analysis and next-generation sequencing in pre-therapeutic biopsies.

Journal Of Cancer Research And Clinical Oncology

Kleo, Karsten K; Jovanovic, Vladimir M VM; Arndold, Alexander A; Lehmann, Annika A; Lammert, Hedwig H; Berg, Erika E; Harloff, Hannah H; Treese, Christoph C; Hummel, Michael M; Daum, Severin S

Publication Date: 2022-03-05

Variant appearance in text: rs214955

PubMed Link: 35246724

Variant Present in the following documents:

• 432_2022_3944_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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Comprehensive Insights Into Forensic Features and Genetic Background of Chinese Northwest Hui Group Using Six Distinct Categories of 231 Molecular Markers.

Frontiers In Genetics

Chen, Chong C; Jin, Xiaoye X; Zhang, Xingru X; Zhang, Wenqing W; Guo, Yuxin Y; Tao, Ruiyang R; Chen, Anqi A; Xu, Qiannan Q; Li, Min M; Yang, Yue Y; Zhu, Bofeng B

Publication Date: 2021

Variant appearance in text: rs214955

PubMed Link: 34721519

Variant Present in the following documents:

• Main text
• fgene-12-705753.pdf

View BVdb publication page

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Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology

Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA

Publication Date: 2021

Variant appearance in text: rs214955

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Confirmation of Paternity despite Three Genetic Incompatibilities at Chromosome 2.

Genes

Doniec, Andrzej A; Łuczak, Wojciech W; Wróbel, Maria M; Januła, Miłosz M; Ossowski, Andrzej A; Grzmil, Paweł P; Kupiec, Tomasz T

Publication Date: 2021-01-04

Variant appearance in text: rs214955

PubMed Link: 33406744

Variant Present in the following documents:

• Main text
• genes-12-00062.pdf

View BVdb publication page

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: rs214955

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology

Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S

Publication Date: 2019-10-22

Variant appearance in text: rs214955

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: rs214955

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1

View BVdb publication page

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Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report.

Bmc Neurology

Zhang, Xiaoqian X; Zhang, Lei L; Wu, Yanqing Y; Li, Gang G; Chen, Shengcai S; Xia, Yuanpeng Y; Li, Hongge H

Publication Date: 2018-11-29

Variant appearance in text: rs214955

PubMed Link: 30497413

Variant Present in the following documents:

• 12883_2018_1199_MOESM5_ESM.xlsx, sheet 1

View BVdb publication page

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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: rs214955

PubMed Link: 30319441

Variant Present in the following documents:

• Table_6.xlsx, sheet 1

View BVdb publication page

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Metaplastic breast cancer in a patient with neurofibromatosis type 1 and somatic loss of heterozygosity.

Cold Spring Harbor Molecular Case Studies

Suarez-Kelly, Lorena P LP; Akagi, Keiko K; Reeser, Julie W JW; Samorodnitsky, Eric E; Reeder, Matthew M; Smith, Amy A; Roychowdhury, Sameek S; Symer, David E DE; Carson, William E WE

Publication Date: 2018-04

Variant appearance in text: rs214955

PubMed Link: 29449315

Variant Present in the following documents:

• supp_mcs.a002352_Supplemental_Table_3.xls, sheet 1

View BVdb publication page

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Qualitative and quantitative assessment of Illumina's forensic STR and SNP kits on MiSeq FGx™.

Plos One

Sharma, Vishakha V; Chow, Hoi Yan HY; Siegel, Donald D; Wurmbach, Elisa E

Publication Date: 2017

Variant appearance in text: rs214955

PubMed Link: 29121662

Variant Present in the following documents:

• Main text
• pone.0187932.pdf

View BVdb publication page

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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: rs214955

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Comparison of Two Massively Parallel Sequencing Platforms using 83 Single Nucleotide Polymorphisms for Human Identification.

Scientific Reports

Apaga, Dame Loveliness T DL; Dennis, Sheila E SE; Salvador, Jazelyn M JM; Calacal, Gayvelline C GC; De Ungria, Maria Corazon A MC

Publication Date: 2017-03-24

Variant appearance in text: rs214955

PubMed Link: 28341840

Variant Present in the following documents:

• Main text
• 41598_2017_Article_510.pdf

View BVdb publication page

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Simultaneous genomic identification and profiling of a single cell using semiconductor-based next generation sequencing.

Applied & Translational Genomics

Watanabe, Manabu M; Kusano, Junko J; Ohtaki, Shinsaku S; Ishikura, Takashi T; Katayama, Jin J; Koguchi, Akira A; Paumen, Michael M; Hayashi, Yoshiharu Y

Publication Date: 2014-09-01

Variant appearance in text: rs214955

PubMed Link: 27294018

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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Parallel Analysis of 124 Universal SNPs for Human Identification by Targeted Semiconductor Sequencing.

Scientific Reports

Zhang, Suhua S; Bian, Yingnan Y; Zhang, Zheren Z; Zheng, Hancheng H; Wang, Zheng Z; Zha, Lagabaiyila L; Cai, Jifeng J; Gao, Yuzhen Y; Ji, Chaoneng C; Hou, Yiping Y; Li, Chengtao C

Publication Date: 2015-12-22

Variant appearance in text: rs214955

PubMed Link: 26691610

Variant Present in the following documents:

• Main text
• srep18683.pdf

View BVdb publication page

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Allele frequencies for 40 autosomal SNP loci typed for US population samples using electrospray ionization mass spectrometry.

Croatian Medical Journal

Kiesler, Kevin M KM; Vallone, Peter M PM

Publication Date: 2013-06

Variant appearance in text: rs214955

PubMed Link: 23771752

Variant Present in the following documents:

• Main text
• CroatMedJ_54_0225.pdf

View BVdb publication page

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