Publications:

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Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis.

Scientific Reports

Slavec, Lara L; Karas Kuželički, Nataša N; Locatelli, Igor I; Geršak, Ksenija K

Publication Date: 2022-01-24

Variant appearance in text: rs566926

PubMed Link: 35075162

Variant Present in the following documents:

• Main text
• 41598_2021_Article_2159.pdf

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Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis.

Scientific Reports

Slavec, Lara L; Karas Kuželički, Nataša N; Locatelli, Igor I; Geršak, Ksenija K

Publication Date: 2022-01-24

Variant appearance in text: rs566926

PubMed Link: 35075162

Variant Present in the following documents:

• Main text
• 41598_2021_Article_2159.pdf

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Association of Wnt9B rs1530364 and Wnt5A rs566926 Gene Polymorphisms with Nonsyndromic Cleft lip and Palate in South Indian Population using Deoxyribonucleic Acid Sequencing.

Contemporary Clinical Dentistry

Jain, Rohit R; Dharma, R M RM; Dinesh, M R MR; Amarnath, B C BC; Hegde, Manjunath M; Pramod, K M KM

Publication Date: 2020

Variant appearance in text: rs566926

PubMed Link: 33110311

Variant Present in the following documents:

• Main text
• CCD-11-60.pdf

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[Evaluating the effect of WNT pathway genes considering interactions on the risk of non-syndromic oral clefts among Chinese populations].

Beijing Da Xue Xue Bao. Yi Xue Ban = Journal Of Peking University. Health Sciences

Wang, M Y MY; Li, W Y WY; Zhou, R R; Wang, S Y SY; Liu, D J DJ; Zheng, H C HC; Li, J J; Li, N N; Zhou, Z B ZB; Zhu, H P HP; Wu, T T; Hu, Y H YH

Publication Date: 2020-10-18

Variant appearance in text: rs566926

PubMed Link: 33047713

Variant Present in the following documents:

• Main text

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WNT gene polymorphisms and predisposition to apical periodontitis.

Scientific Reports

de Souza, Letícia Chaves LC; Cavalla, Franco F; Maili, Lorena L; Garlet, Gustavo P GP; Vieira, Alexandre R AR; Silva, Renato M RM; Letra, Ariadne A

Publication Date: 2019-12-12

Variant appearance in text: rs566926

PubMed Link: 31831777

Variant Present in the following documents:

• Main text
• 41598_2019_Article_55293.pdf

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Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.

Plos One

Bakhchane, Amina A; Charif, Majida M; Bousfiha, Amale A; Boulouiz, Redouane R; Nahili, Halima H; Rouba, Hassan H; Charoute, Hicham H; Lenaers, Guy G; Barakat, Abdelhamid A

Publication Date: 2017

Variant appearance in text: rs566926

PubMed Link: 28472130

Variant Present in the following documents:

• pone.0176516.s002.xlsx, sheet 1

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Pathway Analyses Identify Novel Variants in the WNT Signaling Pathway Associated with Tuberculosis in Chinese Population.

Scientific Reports

Hu, Xuejiao X; Zhou, Juan J; Chen, Xuerong X; Zhou, Yanhong Y; Song, Xingbo X; Cai, Bei B; Zhang, Jingya J; Lu, Xiaojun X; Ying, Binwu B

Publication Date: 2016-06-23

Variant appearance in text: rs566926

PubMed Link: 27334567

Variant Present in the following documents:

• Main text
• srep28530.pdf

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Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population.

Scientific Reports

Li, Peiqiang P; Li, Haijie H; Zheng, Yufang Y; Qiao, Bin B; Duan, Wenyuan W; Huang, Lijuan L; Liu, Weiqi W; Wang, Hongyan H

Publication Date: 2015-08-17

Variant appearance in text: rs566926

PubMed Link: 26278011

Variant Present in the following documents:

• Main text
• srep13120.pdf

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Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.

The Pharmacogenomics Journal

Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X

Publication Date: 2014-12

Variant appearance in text: rs566926

PubMed Link: 24980784

Variant Present in the following documents:

• Main text

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Genetic variants of the Wnt signaling pathway as predictors of recurrence and survival in early-stage non-small cell lung cancer patients.

Carcinogenesis

Coscio, Angela A; Chang, David W DW; Roth, Jack A JA; Ye, Yuanqing Y; Gu, Jian J; Yang, Ping P; Wu, Xifeng X

Publication Date: 2014-06

Variant appearance in text: rs566926

PubMed Link: 24517998

Variant Present in the following documents:

• Main text

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Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families.

The Cleft Palate-Craniofacial Journal : Official Publication Of The American Cleft Palate-Craniofacial Association

Fontoura, Clarissa C; Silva, Renato M RM; Granjeiro, José M JM; Letra, Ariadne A

Publication Date: 2015-01

Variant appearance in text: rs566926

PubMed Link: 24437584

Variant Present in the following documents:

• Main text

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Haplotype association analysis of genes within the WNT signalling pathways in diabetic nephropathy.

Bmc Nephrology

Kavanagh, David H DH; Savage, David A DA; Patterson, Christopher C CC; McKnight, Amy Jayne AJ; Crean, John K JK; Maxwell, Alexander P AP; McKay, Gareth J GJ; ,

Publication Date: 2013-06-18

Variant appearance in text: rs566926

PubMed Link: 23777469

Variant Present in the following documents:

• Main text
• 1471-2369-14-126.pdf

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Insights from studies with oral cleft genes suggest associations between WNT-pathway genes and risk of oral cancer.

Journal Of Dental Research

Andrade Filho, P A PA; Letra, A A; Cramer, A A; Prasad, J L JL; Garlet, G P GP; Vieira, A R AR; Ferris, R L RL; Menezes, R R

Publication Date: 2011-06

Variant appearance in text: rs566926

PubMed Link: 21393552

Variant Present in the following documents:

• Main text

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Studies with Wnt genes and nonsyndromic cleft lip and palate.

Birth Defects Research. Part A, Clinical And Molecular Teratology

Menezes, Renato R; Letra, Ariadne A; Kim, Ana H AH; Küchler, Erika C EC; Day, Alicia A; Tannure, Patricia N PN; Gomes da Motta, Luise L; Paiva, Katiucia B S KB; Granjeiro, Jose M JM; Vieira, Alexandre R AR

Publication Date: 2010-11

Variant appearance in text: rs566926

PubMed Link: 20890934

Variant Present in the following documents:

• Main text

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Analysis of eight genes modulating interferon gamma and human genetic susceptibility to tuberculosis: a case-control association study.

Bmc Infectious Diseases

Möller, Marlo M; Nebel, Almut A; van Helden, Paul D PD; Schreiber, Stefan S; Hoal, Eileen G EG

Publication Date: 2010-06-07

Variant appearance in text: rs566926

PubMed Link: 20525402

Variant Present in the following documents:

• Main text
• 1471-2334-10-154.pdf

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Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.

Human Molecular Genetics

Chiquet, Brett T BT; Blanton, Susan H SH; Burt, Amber A; Ma, Deqiong D; Stal, Samuel S; Mulliken, John B JB; Hecht, Jacqueline T JT

Publication Date: 2008-07-15

Variant appearance in text: rs566926

PubMed Link: 18413325

Variant Present in the following documents:

• Main text

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