RELN c.2989C>A ;(p.L997I)

Variant ID: 7-103251161-G-T

NM_005045.3(RELN):c.2989C>A;(p.L997I)

This variant was identified in 26 publications

View GRCh38 version.




Publications:


Working memory deficits in children with schizophrenia and its mechanism, susceptibility genes, and improvement: A literature review.

Frontiers In Psychiatry
Zhou, Jintao J; Li, Jingfangzhou J; Zhao, Qi Q; Ou, Peixin P; Zhao, Wan W
Publication Date: 2022

Variant appearance in text: rs362691
PubMed Link: 35990059
Variant Present in the following documents:
  • Main text
  • fpsyt-13-899344.pdf
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SNP-PCR genotyping links alterations in the GABAA receptor (GABRG3: rs208129) and RELN (rs73670) genes to autism spectrum disorder among peadiatric Iraqi Arabs.

Molecular Biology Reports
Ali, Zainab A ZA; Yasseen, Akeel A AA; McAllister, Katherine A KA; Al-Dujailli, Arafat A; Al-Karaqully, Ahmed J AJ; Jumaah, Alaa S AS
Publication Date: 2022-07

Variant appearance in text: rs362691
PubMed Link: 35403940
Variant Present in the following documents:
  • Main text
  • 11033_2022_Article_7388.pdf
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A systematic review of common genetic variation and biological pathways in autism spectrum disorder.

Bmc Neuroscience
Rodriguez-Gomez, Diego Alejandro DA; Garcia-Guaqueta, Danna Paola DP; Charry-Sánchez, Jesús David JD; Sarquis-Buitrago, Elias E; Blanco, Mariana M; Velez-van-Meerbeke, Alberto A; Talero-Gutiérrez, Claudia C
Publication Date: 2021-10-09

Variant appearance in text: rs362691
PubMed Link: 34627165
Variant Present in the following documents:
  • 12868_2021_662_MOESM1_ESM.xlsx, sheet 1
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Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies.

International Journal Of Environmental Research And Public Health
Hernández-García, Ignacio I; Chamorro, Antonio-Javier AJ; Ternavasio-de la Vega, Hugo Guillermo HG; Carbonell, Cristina C; Marcos, Miguel M; Mirón-Canelo, José-Antonio JA
Publication Date: 2020-10-30

Variant appearance in text: rs362691
PubMed Link: 33143244
Variant Present in the following documents:
  • Main text
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Genetic Variation and Autism: A Field Synopsis and Systematic Meta-Analysis.

Brain Sciences
Lee, Jinhee J; Son, Min Ji MJ; Son, Chei Yun CY; Jeong, Gwang Hun GH; Lee, Keum Hwa KH; Lee, Kwang Seob KS; Ko, Younhee Y; Kim, Jong Yeob JY; Lee, Jun Young JY; Radua, Joaquim J; Eisenhut, Michael M; Gressier, Florence F; Koyanagi, Ai A; Stubbs, Brendon B; Solmi, Marco M; Rais, Theodor B TB; Kronbichler, Andreas A; Dragioti, Elena E; Vasconcelos, Daniel Fernando Pereira DFP; Silva, Felipe Rodolfo Pereira da FRPD; Tizaoui, Kalthoum K; Brunoni, André Russowsky AR; Carvalho, Andre F AF; Cargnin, Sarah S; Terrazzino, Salvatore S; Stickley, Andrew A; Smith, Lee L; Thompson, Trevor T; Shin, Jae Il JI; Fusar-Poli, Paolo P
Publication Date: 2020-09-30

Variant appearance in text: rs362691
PubMed Link: 33007889
Variant Present in the following documents:
  • Main text
  • brainsci-10-00692.pdf
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Genetic and Epigenetic Etiology Underlying Autism Spectrum Disorder.

Journal Of Clinical Medicine
Yoon, Sang Hoon SH; Choi, Joonhyuk J; Lee, Won Ji WJ; Do, Jeong Tae JT
Publication Date: 2020-03-31

Variant appearance in text: rs362691
PubMed Link: 32244359
Variant Present in the following documents:
  • Main text
  • jcm-09-00966.pdf
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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: rs362691
PubMed Link: 30891068
Variant Present in the following documents:
  • Main text
  • fgene-10-00175.pdf
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Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery.

American Journal Of Perinatology
Varner, Michael W MW; Costantine, Maged M MM; Jablonski, Kathleen A KA; Rouse, Dwight J DJ; Mercer, Brian M BM; Leveno, Kenneth J KJ; Reddy, Uma M UM; Buhimschi, Catalin C; Wapner, Ronald J RJ; Sorokin, Yoram Y; Thorp, John M JM; Ramin, Susan M SM; Malone, Fergal D FD; Carpenter, Marshall M; O'sullivan, Mary J MJ; Peaceman, Alan M AM; Dudley, Donald J DJ; Caritis, Steve N SN; ,
Publication Date: 2020-02

Variant appearance in text: rs362691
PubMed Link: 30731481
Variant Present in the following documents:
  • Main text
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Development of an AmpliSeqTM Panel for Next-Generation Sequencing of a Set of Genetic Predictors of Persisting Pain.

Frontiers In Pharmacology
Kringel, Dario D; Kaunisto, Mari A MA; Lippmann, Catharina C; Kalso, Eija E; Lötsch, Jörn J
Publication Date: 2018

Variant appearance in text: rs362691
PubMed Link: 30283335
Variant Present in the following documents:
  • Main text
  • fphar-09-01008.pdf
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Imaging genetics in neurodevelopmental psychopathology.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Klein, Marieke M; van Donkelaar, Marjolein M; Verhoef, Ellen E; Franke, Barbara B
Publication Date: 2017-07

Variant appearance in text: rs362691
PubMed Link: 29984470
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Systematic Review of Research on Autism Spectrum Disorders in Sub-Saharan Africa.

Behavioural Neurology
Abubakar, Amina A; Ssewanyana, Derrick D; Newton, Charles R CR
Publication Date: 2016

Variant appearance in text: rs362691
PubMed Link: 27872512
Variant Present in the following documents:
  • Main text
  • BN2016-3501910.pdf
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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: rs362691
PubMed Link: 27803648
Variant Present in the following documents:
  • Main text
  • fncel-10-00229.pdf
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The Neurobiological Basis for Social Affiliation in Autism Spectrum Disorder and Schizophrenia.

Current Behavioral Neuroscience Reports
Crider, Amanda A; Pillai, Anilkumar A
Publication Date: 2016-06

Variant appearance in text: rs362691
PubMed Link: 27695666
Variant Present in the following documents:
  • Main text
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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: rs362691
PubMed Link: 27081382
Variant Present in the following documents:
  • Main text
  • pi-13-210.pdf
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RELN Mutations in Autism Spectrum Disorder.

Frontiers In Cellular Neuroscience
Lammert, Dawn B DB; Howell, Brian W BW
Publication Date: 2016

Variant appearance in text: rs362691
PubMed Link: 27064498
Variant Present in the following documents:
  • Main text
  • fncel-10-00084.pdf
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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: rs362691
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
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Poster Session IIIWednesday, December 9, 2015.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology
Publication Date: 2015-12

Variant appearance in text: rs362691
PubMed Link: 26632288
Variant Present in the following documents:
  • Main text
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A comprehensive meta-analysis of common genetic variants in autism spectrum conditions.

Molecular Autism
Warrier, Varun V; Chee, Vivienne V; Smith, Paula P; Chakrabarti, Bhismadev B; Baron-Cohen, Simon S
Publication Date: 2015

Variant appearance in text: rs362691
PubMed Link: 26322220
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10.

Molecular Autism
Jonsson, Lina L; Zettergren, Anna A; Pettersson, Erik E; Hovey, Daniel D; Anckarsäter, Henrik H; Westberg, Lars L; Lichtenstein, Paul P; Lundström, Sebastian S; Melke, Jonas J
Publication Date: 2014

Variant appearance in text: rs362691
PubMed Link: 25540679
Variant Present in the following documents:
  • Main text
  • 13229_2014_Article_146.pdf
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An evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autism.

Frontiers In Endocrinology
Berbel, Pere P; Navarro, Daniela D; Román, Gustavo C GC
Publication Date: 2014

Variant appearance in text: rs362691
PubMed Link: 25250016
Variant Present in the following documents:
  • Main text
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NCI-60 whole exome sequencing and pharmacological CellMiner analyses.

Plos One
Reinhold, William C WC; Varma, Sudhir S; Sousa, Fabricio F; Sunshine, Margot M; Abaan, Ogan D OD; Davis, Sean R SR; Reinhold, Spencer W SW; Kohn, Kurt W KW; Morris, Joel J; Meltzer, Paul S PS; Doroshow, James H JH; Pommier, Yves Y
Publication Date: 2014

Variant appearance in text: rs362691
PubMed Link: 25032700
Variant Present in the following documents:
  • pone.0101670.s004.xlsx, sheet 1
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Epilepsy: Indian perspective.

Annals Of Indian Academy Of Neurology
Santhosh, Nandanavana Subbareddy NS; Sinha, Sanjib S; Satishchandra, Parthasarathy P
Publication Date: 2014-03

Variant appearance in text: rs362691
PubMed Link: 24791085
Variant Present in the following documents:
  • Main text
  • AIAN-17-3.pdf
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Neurodevelopment in schizophrenia: the role of the wnt pathways.

Current Neuropharmacology
Panaccione, Isabella I; Napoletano, Flavia F; Forte, Alberto Maria AM; Kotzalidis, Giorgio D GD; Del Casale, Antonio A; Rapinesi, Chiara C; Brugnoli, Chiara C; Serata, Daniele D; Caccia, Federica F; Cuomo, Ilaria I; Ambrosi, Elisa E; Simonetti, Alessio A; Savoja, Valeria V; De Chiara, Lavinia L; Danese, Emanuela E; Manfredi, Giovanni G; Janiri, Delfina D; Motolese, Marta M; Nicoletti, Ferdinando F; Girardi, Paolo P; Sani, Gabriele G
Publication Date: 2013-09

Variant appearance in text: rs362691
PubMed Link: 24403877
Variant Present in the following documents:
  • Main text
  • CN-11-535.pdf
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Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.

Genetic Testing And Molecular Biomarkers
Sharma, Jyoti Rajan JR; Arieff, Zainunisha Z; Gameeldien, Hajirah H; Davids, Muneera M; Kaur, Mandeep M; van der Merwe, Lize L
Publication Date: 2013-02

Variant appearance in text: rs362691
PubMed Link: 23216241
Variant Present in the following documents:
  • Main text
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The involvement of Reelin in neurodevelopmental disorders.

Neuropharmacology
Folsom, Timothy D TD; Fatemi, S Hossein SH
Publication Date: 2013-05

Variant appearance in text: rs362691
PubMed Link: 22981949
Variant Present in the following documents:
  • Main text
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Association of polymorphisms in neuroprotection and oxidative stress genes and neurodevelopmental outcomes after preterm birth.

Obstetrics And Gynecology
Costantine, Maged M MM; Clark, Erin A S EA; Lai, Yinglei Y; Rouse, Dwight J DJ; Spong, Catherine Y CY; Mercer, Brian M BM; Sorokin, Yoram Y; Thorp, John M JM; Ramin, Susan M SM; Malone, Fergal D FD; Carpenter, Marshall M; Miodovnik, Menachem M; O'Sullivan, Mary J MJ; Peaceman, Alan M AM; Caritis, Steve N SN
Publication Date: 2012-09

Variant appearance in text: rs362691
PubMed Link: 22914463
Variant Present in the following documents:
  • Main text
View BVdb publication page