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: rs362726

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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The Pathophysiological Link Between Reelin and Autism: Overview and New Insights.

Frontiers In Genetics

Scala, Marcello M; Grasso, Eleonora A EA; Di Cara, Giuseppe G; Riva, Antonella A; Striano, Pasquale P; Verrotti, Alberto A

Publication Date: 2022

Variant appearance in text: rs362726

PubMed Link: 35422848

Variant Present in the following documents:

• Main text
• fgene-13-869002.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: rs362726

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Two Novel Loci of RELN Associated With Antipsychotics Response in Chinese Han Population.

Frontiers In Pharmacology

Xu, Qingqing Q; Li, Mo M; Qin, Shengying S; Li, Yaojing Y; Ning, Ailing A; Fu, Yingmei Y; Wang, Dongxiang D; Zeng, Duan D; Li, Huafang H; Yu, Wenjuan W; Yu, Shunying S

Publication Date: 2020

Variant appearance in text: rs362726

PubMed Link: 32082176

Variant Present in the following documents:

• Main text
• fphar-11-00007.pdf

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: RELN: 4589-28A>G; rs362726

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: rs362726

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1

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SNP Variation of RELN Gene and Schizophrenia in a Chinese Population: A Hospital-Based Case-Control Study.

Frontiers In Genetics

Luo, Xia X; Chen, Si S; Xue, Li L; Chen, Jian-Huan JH; Shi, Yan-Wei YW; Zhao, Hu H

Publication Date: 2019

Variant appearance in text: rs362726

PubMed Link: 30891068

Variant Present in the following documents:

• Main text
• fgene-10-00175.pdf

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: RELN: 4589-28A>G; rs362726

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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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: rs362726

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Reelin and Neuropsychiatric Disorders.

Frontiers In Cellular Neuroscience

Ishii, Kazuhiro K; Kubo, Ken-Ichiro KI; Nakajima, Kazunori K

Publication Date: 2016

Variant appearance in text: rs362726

PubMed Link: 27803648

Variant Present in the following documents:

• Main text
• fncel-10-00229.pdf

View BVdb publication page

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Association between RELN Gene Polymorphisms and Attention Deficit Hyperactivity Disorder in Korean Children.

Psychiatry Investigation

Kwon, Ho Jang HJ; Jang, Won-Cheol WC; Lim, Myung Ho MH

Publication Date: 2016-03

Variant appearance in text: rs362726

PubMed Link: 27081382

Variant Present in the following documents:

• Main text
• pi-13-210.pdf

View BVdb publication page

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Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports

Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC

Publication Date: 2015-12-08

Variant appearance in text: rs362726

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 3
• mmc3.xlsx, sheet 2
• mmc3.xlsx, sheet 1

View BVdb publication page

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Sex-specific association of the Reelin gene with bipolar disorder.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Goes, F S FS; Willour, V L VL; Zandi, P P PP; Belmonte, P L PL; MacKinnon, D F DF; Mondimore, F M FM; Schweizer, B B; , ; DePaulo, J R JR; Gershon, E S ES; McMahon, F J FJ; Potash, J B JB

Publication Date: 2010-03-05

Variant appearance in text: rs362726

PubMed Link: 19691043

Variant Present in the following documents:

• Main text

View BVdb publication page

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