Publications:

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A case of midbrain germinoma: A literature review for radiographic and clinical features.

Neuro-Oncology Advances

Miyake, Yohei Y; Tateishi, Kensuke K; Oshima, Akito A; Hongo, Takeshi T; Satomi, Kaishi K; Ichimura, Koichi K; Kato, Ayumi A; Iwashita, Hiromichi H; Utsunomiya, Daisuke D; Yamamoto, Tetsuya T

Publication Date: 2023

Variant appearance in text: rs216312

PubMed Link: 37215953

Variant Present in the following documents:

• vdad043_suppl_supplementary_tables.xlsx, sheet 1

View BVdb publication page

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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: rs216312

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics

Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F

Publication Date: 2021

Variant appearance in text: VWF: 3675-75A>G; rs216312

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.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: VWF: 3675-75A>G; rs216312

PubMed Link: 30319441

Variant Present in the following documents:

• Table_6.xlsx, sheet 1
• Table_7.xlsx, sheet 1

View BVdb publication page

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Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.

Nature Communications

Schrader, A A; Crispatzu, G G; Oberbeck, S S; Mayer, P P; Pützer, S S; von Jan, J J; Vasyutina, E E; Warner, K K; Weit, N N; Pflug, N N; Braun, T T; Andersson, E I EI; Yadav, B B; Riabinska, A A; Maurer, B B; Ventura Ferreira, M S MS; Beier, F F; Altmüller, J J; Lanasa, M M; Herling, C D CD; Haferlach, T T; Stilgenbauer, S S; Hopfinger, G G; Peifer, M M; Brümmendorf, T H TH; Nürnberg, P P; Elenitoba-Johnson, K S J KSJ; Zha, S S; Hallek, M M; Moriggl, R R; Reinhardt, H C HC; Stern, M-H MH; Mustjoki, S S; Newrzela, S S; Frommolt, P P; Herling, M M

Publication Date: 2018-02-15

Variant appearance in text: rs216312

PubMed Link: 29449575

Variant Present in the following documents:

• 41467_2017_2688_MOESM14_ESM.xls, sheet 2
• 41467_2017_2688_MOESM14_ESM.xls, sheet 3

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: rs216312

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Von Willebrand Factor Gene Variants Associate with Herpes simplex Encephalitis.

Plos One

Abdelmagid, Nada N; Bereczky-Veress, Biborka B; Atanur, Santosh S; Musilová, Alena A; Zídek, Václav V; Saba, Laura L; Warnecke, Andreas A; Khademi, Mohsen M; Studahl, Marie M; Aurelius, Elisabeth E; Hjalmarsson, Anders A; Garcia-Diaz, Ana A; Denis, Cécile V CV; Bergström, Tomas T; Sköldenberg, Birgit B; Kockum, Ingrid I; Aitman, Timothy T; Hübner, Norbert N; Olsson, Tomas T; Pravenec, Michal M; Diez, Margarita M

Publication Date: 2016

Variant appearance in text: rs216312

PubMed Link: 27224245

Variant Present in the following documents:

• Main text
• pone.0155832.pdf

View BVdb publication page

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Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.

The Indian Journal Of Medical Research

Kasatkar, Priyanka P; Ghosh, Kanjaksha K; Shetty, Shrimati S

Publication Date: 2015-12

Variant appearance in text: rs216312

PubMed Link: 26831425

Variant Present in the following documents:

• Main text
• IJMR-142-759.pdf

View BVdb publication page

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Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One

Holehouse, Alex S AS; Naegle, Kristen M KM

Publication Date: 2015

Variant appearance in text: rs216312

PubMed Link: 26659599

Variant Present in the following documents:

• pone.0144692.s002.xlsx, sheet 1

View BVdb publication page

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Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort.

Haematologica

Hampshire, Daniel J DJ; Burghel, George J GJ; Goudemand, Jenny J; Bouvet, Laura C S LC; Eikenboom, Jeroen C J JC; Schneppenheim, Reinhard R; Budde, Ulrich U; Peake, Ian R IR; Goodeve, Anne C AC; ,

Publication Date: 2010-12

Variant appearance in text: VWF: 3675-75A>G; rs216312

PubMed Link: 20851871

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.

Gastroenterology

Roberts, Kari E KE; Kawut, Steven M SM; Krowka, Michael J MJ; Brown, Robert S RS; Trotter, James F JF; Shah, Vijay V; Peter, Inga I; Tighiouart, Hocine H; Mitra, Nandita N; Handorf, Elizabeth E; Knowles, James A JA; Zacks, Steven S; Fallon, Michael B MB; ,

Publication Date: 2010-07

Variant appearance in text: rs216312

PubMed Link: 20346360

Variant Present in the following documents:

• Main text

View BVdb publication page

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