Publications:

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US Population Data for 94 Identity-Informative SNP Loci.

Genes

Kiesler, Kevin M KM; Borsuk, Lisa A LA; Steffen, Carolyn R CR; Vallone, Peter M PM; Gettings, Katherine B KB

Publication Date: 2023-05-12

Variant appearance in text: rs1736442

PubMed Link: 37239431

Variant Present in the following documents:

• Main text
• genes-14-01071.pdf

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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: rs1736442

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Sequencing of human identification markers in an Uyghur population using the MiSeq FGxTM Forensic Genomics System.

Forensic Sciences Research

Simayijiang, Halimureti H; Morling, Niels N; Børsting, Claus C

Publication Date: 2022

Variant appearance in text: rs1736442

PubMed Link: 35784409

Variant Present in the following documents:

• Main text
• TFSR_7_1779967.pdf

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Validation and beyond: Next generation sequencing of forensic casework samples including challenging tissue samples from altered human corpses using the MiSeq FGx system.

Journal Of Forensic Sciences

Senst, Alina A; Caliebe, Amke A; Scheurer, Eva E; Schulz, Iris I

Publication Date: 2022-07

Variant appearance in text: rs1736442

PubMed Link: 35318655

Variant Present in the following documents:

• Main text
• JFO-67-1382.pdf

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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: FECH: 804+600A>G; rs1736442

PubMed Link: 35246724

Variant Present in the following documents:

• 432_2022_3944_MOESM1_ESM.xlsx, sheet 1

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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: rs1736442

PubMed Link: 34721519

Variant Present in the following documents:

• Main text
• fgene-12-705753.pdf

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Evaluation and SNP typing of DNA from ultraviolet-irradiated human bloodstains using TaqMan assay.

Scientific Reports

Tie, Jian J; Uchigasaki, Seisaku S; Isobe, Eiji E

Publication Date: 2021-04-13

Variant appearance in text: rs1736442

PubMed Link: 33850175

Variant Present in the following documents:

• Main text
• 41598_2021_Article_87313.pdf

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Evaluation of OpenArray™ as a Genotyping Method for Forensic DNA Phenotyping and Human Identification.

Genes

Ragazzo, Michele M; Puleri, Giulio G; Errichiello, Valeria V; Manzo, Laura L; Luzzi, Laura L; Potenza, Saverio S; Strafella, Claudia C; Peconi, Cristina C; Nicastro, Fabio F; Caputo, Valerio V; Giardina, Emiliano E

Publication Date: 2021-02-03

Variant appearance in text: rs1736442

PubMed Link: 33546406

Variant Present in the following documents:

• Main text
• genes-12-00221.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: rs1736442

PubMed Link: 33406744

Variant Present in the following documents:

• Main text
• genes-12-00062.pdf

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The mutational load and a T-cell inflamed tumour phenotype identify ovarian cancer patients rendering tumour-reactive T cells from PD-1+ tumour-infiltrating lymphocytes.

British Journal Of Cancer

Salas-Benito, Diego D; Conde, Enrique E; Tamayo-Uria, Ibon I; Mancheño, Uxua U; Elizalde, Edurne E; Garcia-Ros, David D; Aramendia, Jose M JM; Muruzabal, Juan C JC; Alcaide, Julia J; Guillen-Grima, Francisco F; Minguez, Jose A JA; Amores-Tirado, Jose J; Gonzalez-Martin, Antonio A; Sarobe, Pablo P; Lasarte, Juan J JJ; Ponz-Sarvise, Mariano M; De Andrea, Carlos E CE; Hervas-Stubbs, Sandra S

Publication Date: 2021-03

Variant appearance in text: FECH: 804+600A>G; rs1736442

PubMed Link: 33402737

Variant Present in the following documents:

• 41416_2020_1218_MOESM2_ESM.xlsx, sheet 1

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Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA.

International Journal Of Legal Medicine

Müller, Petra P; Sell, Christian C; Hadrys, Thorsten T; Hedman, Johannes J; Bredemeyer, Steffi S; Laurent, Francois-Xavier FX; Roewer, Lutz L; Achtruth, Sabrina S; Sidstedt, Maja M; Sijen, Titia T; Trimborn, Marc M; Weiler, Natalie N; Willuweit, Sascha S; Bastisch, Ingo I; Parson, Walther W; ,

Publication Date: 2020-01

Variant appearance in text: rs1736442

PubMed Link: 31745634

Variant Present in the following documents:

• Main text
• 414_2019_Article_2201.pdf

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Sequencing of 231 forensic genetic markers using the MiSeq FGx™ forensic genomics system - an evaluation of the assay and software.

Forensic Sciences Research

Hussing, Christian C; Huber, Christina C; Bytyci, Rajmonda R; Mogensen, Helle S HS; Morling, Niels N; Børsting, Claus C

Publication Date: 2018

Variant appearance in text: rs1736442

PubMed Link: 30483659

Variant Present in the following documents:

• Main text
• tfsr-3-1446672.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: rs1736442

PubMed Link: 29121662

Variant Present in the following documents:

• Main text
• pone.0187932.pdf

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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: rs1736442

PubMed Link: 28341840

Variant Present in the following documents:

• Main text
• 41598_2017_Article_510.pdf

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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: rs1736442

PubMed Link: 27294018

Variant Present in the following documents:

• Main text
• main.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: rs1736442

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: rs1736442

PubMed Link: 26522768

Variant Present in the following documents:

• Main text
• alm-36-82.pdf

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