Publications:

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs9905977

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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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: rs9905977

PubMed Link: 35246724

Variant Present in the following documents:

• 432_2022_3944_MOESM1_ESM.xlsx, sheet 1

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Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT.

Plos One

Zhuo, Xinming X; Wang, Qun Q; Vossaert, Liesbeth L; Salman, Roseen R; Kim, Adriel A; Van den Veyver, Ignatia I; Breman, Amy A; Beaudet, Arthur A

Publication Date: 2021

Variant appearance in text: rs9905977

PubMed Link: 33857205

Variant Present in the following documents:

• Main text
• pone.0249695.pdf

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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: rs9905977

PubMed Link: 33406744

Variant Present in the following documents:

• Main text
• genes-12-00062.pdf

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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: rs9905977

PubMed Link: 29121662

Variant Present in the following documents:

• Main text
• pone.0187932.pdf

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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: rs9905977

PubMed Link: 26691610

Variant Present in the following documents:

• Main text
• srep18683.pdf

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Bone marrow chimerism detection using next generation sequencing based on single nucleotide polymorphisms following liver transplantation: comparison with short tandem repeat-PCR.

Annals Of Laboratory Medicine

Kim, Jieun J; Hwang, In Sik IS; Kim, Hyon Suk HS; Joo, Dong Jin DJ; Hong, Kyung Ran KR; Choi, Jong Rak JR

Publication Date: 2016-01

Variant appearance in text: rs9905977

PubMed Link: 26522768

Variant Present in the following documents:

• Main text
• alm-36-82.pdf

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