MTRR c.66A>G ;(p.I22M)

Variant ID: 5-7870973-A-G

NM_002454.2(MTRR):c.66A>G;(p.I22M)

This variant was identified in 312 publications

View GRCh38 version.




Publications:


Association of MTR A2756G and MTRR A66G Polymorphisms With Male Infertility: An Updated Meta-Analysis.

American Journal Of Men'S Health
Tariq, Tamjeed T; Arshad, Adina A; Bibi, Ayesha A; Aslam, Shaista S; Sohail, Anam A; Ishaq, Bilal B; Irfan, Muhammad M
Publication Date: 2023

Variant appearance in text: rs1801394
PubMed Link: 37249073
Variant Present in the following documents:
  • Main text
  • 10.1177_15579883231176657.pdf
View BVdb publication page



MTHFR and MTRR Genetic Polymorphism of Methotrexate Therapy Outcomes in Early Rheumatoid Arthritis.

Pharmacogenomics And Personalized Medicine
Zhang, Qian Q; Fu, Pan P; Cao, Zhanglei Z; Huang, Hua H; Wen, Qinwen Q; Wang, Kaizhe K; Kong, Tong T; Wu, Xiudi X; Zheng, Jianping J
Publication Date: 2023

Variant appearance in text: rs1801394
PubMed Link: 37159804
Variant Present in the following documents:
  • Main text
  • pgpm-16-407.pdf
View BVdb publication page



A duplex tetra-primer ARMS-PCR assay to discriminate three species of the Schistosoma haematobium group: Schistosoma curassoni, S. bovis, S. haematobium and their hybrids.

Parasites & Vectors
Blin, Manon M; Dametto, Sarah S; Agniwo, Privat P; Webster, Bonnie L BL; Angora, Etienne E; Dabo, Abdoulaye A; Boissier, Jérôme J
Publication Date: 2023-04-07

Variant appearance in text: MTRR: 66A>G
PubMed Link: 37029440
Variant Present in the following documents:
  • 13071_2023_Article_5754.pdf
View BVdb publication page



Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications
Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA
Publication Date: 2023-04-03

Variant appearance in text: MTRR: I22M
PubMed Link: 37012232
Variant Present in the following documents:
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 3
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2
View BVdb publication page



DNMT3B rs2424913 as a Risk Factor for Congenital Heart Defects in Down Syndrome.

Genes
Majstorović, Dijana D; Barišić, Anita A; Božović, Ivana Babić IB; Čače, Iva Bilić IB; Čače, Neven N; Štifanić, Mauro M; Vraneković, Jadranka J
Publication Date: 2023-02-24

Variant appearance in text: rs1801394
PubMed Link: 36980848
Variant Present in the following documents:
  • Main text
  • genes-14-00576.pdf
View BVdb publication page



Influence of methyl donor nutrients as epigenetic regulators in colorectal cancer: A systematic review of observational studies.

World Journal Of Gastroenterology
Chávez-Hidalgo, Lourdes Pilar LP; Martín-Fernández-de-Labastida, Silvia S; M de Pancorbo, Marian M; Arroyo-Izaga, Marta M
Publication Date: 2023-02-21

Variant appearance in text: rs1801394
PubMed Link: 36926668
Variant Present in the following documents:
  • WJG-29-1219.pdf
View BVdb publication page



Personalized Medicine in Infant Population with Cancer: Pharmacogenetic Pilot Study of Polymorphisms Related to Toxicity and Response to Chemotherapy.

Cancers
Urtasun, Andrea A; Olivera, Gladys G GG; Sendra, Luis L; Aliño, Salvador F SF; Berlanga, Pablo P; Gargallo, Pablo P; Hervás, David D; Balaguer, Julia J; Juan-Ribelles, Antonio A; Andrés, María Del Mar MDM; Cañete, Adela A; Herrero, María José MJ
Publication Date: 2023-02-23

Variant appearance in text: rs1801394
PubMed Link: 36900216
Variant Present in the following documents:
  • cancers-15-01424.pdf
View BVdb publication page



Clinical and genomic features of non-small cell lung cancer occurring in families.

Thoracic Cancer
Miyabe, Shingo S; Ito, Shin S; Sato, Ikuro I; Abe, Jiro J; Tamai, Keiichi K; Mochizuki, Mai M; Fujimori, Haruna H; Yamaguchi, Kazunori K; Shindo, Norihisa N; Shima, Hiroshi H; Yamazaki, Tomoko T; Abue, Makoto M; Okada, Yoshinori Y; Yasuda, Jun J
Publication Date: 2023-03-03

Variant appearance in text: MTRR: I22M
PubMed Link: 36869602
Variant Present in the following documents:
  • TCA-14-940.pdf
View BVdb publication page



Effects of genetic polymorphisms on methotrexate levels and toxicity in Chinese patients with acute lymphoblastic leukemia.

Blood Science (Baltimore, Md.)
Hao, Qishan Q; Song, Yang Y; Fang, Qiuyun Q; Lin, Yani Y; Chen, Long L; Wang, Xiaodan X; Zhang, Ping P; Wang, Zhe Z; Gong, Xiaoyuan X; Liu, Kaiqi K; Li, Qinghua Q; Tian, Zheng Z; Wang, Min M; Wang, Jianxiang J; Mi, Yingchang Y
Publication Date: 2023-01

Variant appearance in text: rs1801394
PubMed Link: 36742186
Variant Present in the following documents:
  • Main text
  • bs9-5-32.pdf
View BVdb publication page



Evolutionary route of nasopharyngeal carcinoma metastasis and its clinical significance.

Nature Communications
Lin, Mei M; Zhang, Xiao-Long XL; You, Rui R; Liu, You-Ping YP; Cai, Hong-Min HM; Liu, Li-Zhi LZ; Liu, Xue-Fei XF; Zou, Xiong X; Xie, Yu-Long YL; Zou, Ru-Hai RH; Zhang, Yi-Nuan YN; Sun, Rui R; Feng, Wei-Yi WY; Wang, Hai-Yan HY; Tao, Gui-Hua GH; Li, Hao-Jiang HJ; Huang, Wen-Jie WJ; Zhang, Chao C; Huang, Pei-Yu PY; Wang, Jin J; Zhao, Qi Q; Yang, Qi Q; Zhang, Hong-Wan HW; Liu, Ting T; Li, Hui-Feng HF; Jiang, Xiao-Bing XB; Tang, Jun J; Gu, Yang-Kui YK; Yu, Tao T; Wang, Zhi-Qiang ZQ; Feng, Lin L; Kang, Tie-Bang TB; Zuo, Zhi-Xiang ZX; Chen, Ming-Yuan MY
Publication Date: 2023-02-04

Variant appearance in text: MTRR: 66A>G; I22M
PubMed Link: 36739462
Variant Present in the following documents:
  • 41467_2023_35995_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Circulating messenger RNA variants as a potential biomarker for surveillance of hepatocellular carcinoma.

Frontiers In Oncology
Block, Timothy T; Zezulinski, Daniel D; Kaplan, David E DE; Lu, Jingqiao J; Zanine, Samantha S; Zhan, Tingting T; Doria, Cataldo C; Sayeed, Aejaz A
Publication Date: 2022

Variant appearance in text: rs1801394
PubMed Link: 36582804
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Association between high-dose methotrexate-induced toxicity and polymorphisms within methotrexate pathway genes in acute lymphoblastic leukemia.

Frontiers In Pharmacology
Xu, Meng M; Wu, Shuangshuang S; Wang, Yue Y; Zhao, Yundong Y; Wang, Ximin X; Wei, Changhong C; Liu, Xueying X; Hao, Feng F; Hu, Cheng C
Publication Date: 2022

Variant appearance in text: rs1801394
PubMed Link: 36532750
Variant Present in the following documents:
  • Main text
  • fphar-13-1003812.pdf
View BVdb publication page



Medical foods for lowering homocysteine in hypertensive patients.

Journal Of Clinical Hypertension (Greenwich, Conn.)
Elias, Merrill F MF; Brown, Craig J CJ
Publication Date: 2022-12-14

Variant appearance in text: rs1801394
PubMed Link: 36519215
Variant Present in the following documents:
  • Main text
  • JCH-25-111.pdf
View BVdb publication page



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: MTRR: I22M; rs1801394
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Identification of SNPs associated with methotrexate treatment outcomes in patients with early rheumatoid arthritis.

Frontiers In Pharmacology
Kolan, Shrikant S SS; Li, Gaoyang G; Grimolizzi, Franco F; Sexton, Joe J; Goll, Guro G; Kvien, Tore K TK; Sundlisæter, Nina Paulshus NP; Zucknick, Manuela M; Lillegraven, Siri S; Haavardsholm, Espen A EA; Skålhegg, Bjørn Steen BS
Publication Date: 2022

Variant appearance in text: rs1801394
PubMed Link: 36467057
Variant Present in the following documents:
  • Main text
  • fphar-13-1075603.pdf
View BVdb publication page



The Roles of MTRR and MTHFR Gene Polymorphisms in Colorectal Cancer Survival.

Nutrients
Wang, Yu Y; Du, Meizhi M; Vallis, Jillian J; Shariati, Matin M; Parfrey, Patrick S PS; Mclaughlin, John R JR; Wang, Peizhong Peter PP; Zhu, Yun Y
Publication Date: 2022-11-01

Variant appearance in text: rs1801394
PubMed Link: 36364857
Variant Present in the following documents:
  • Main text
  • nutrients-14-04594.pdf
View BVdb publication page



Comparison of genetic susceptibility to lung adenocarcinoma and squamous cell carcinoma in Japanese patients using a novel panel for cancer-related drug-metabolizing enzyme genes.

Scientific Reports
Ohnami, Sumiko S; Naruoka, Akane A; Isaka, Mitsuhiro M; Mizuguchi, Maki M; Nakatani, Sou S; Kamada, Fukumi F; Shimoda, Yuji Y; Sakai, Ai A; Ohshima, Keiichi K; Hatakeyama, Keiichi K; Maruyama, Kouji K; Ohde, Yasuhisa Y; Kenmotsu, Hirotsugu H; Takahashi, Toshiaki T; Akiyama, Yasuto Y; Nagashima, Takeshi T; Urakami, Kenichi K; Ohnami, Shumpei S; Yamaguchi, Ken K
Publication Date: 2022-10-26

Variant appearance in text: rs1801394
PubMed Link: 36289279
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_22914.pdf
View BVdb publication page



Genetic susceptibility of bladder cancer in the Lebanese population.

Bmc Medical Genomics
Kourie, Hampig Raphael HR; Succar, Bahaa B; Chouery, Eliane E; Mehawej, Cybel C; Ahmadieh, Nizar N; Zouein, Joseph J; Mardirossian, Avedis A; Jalkh, Nadine N; Sleilaty, Ghassan G; Kattan, Joseph J; Nemr, Elie E
Publication Date: 2022-10-17

Variant appearance in text: MTRR: 66A>G; Ile22Met; rs1801394
PubMed Link: 36253817
Variant Present in the following documents:
  • 12920_2022_1372_MOESM1_ESM.xlsx, sheet 1
  • 12920_2022_1372_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: MTRR: I22M
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM4_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM8_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM7_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
View BVdb publication page



Homocysteine levels, genetic background, and cognitive impairment in Parkinson's disease.

Journal Of Neurology
Periñán, María Teresa MT; Macías-García, Daniel D; Jesús, Silvia S; Martín-Rodríguez, Juan Francisco JF; Muñoz-Delgado, Laura L; Jimenez-Jaraba, Maria Valle MV; Buiza-Rueda, Dolores D; Bonilla-Toribio, Marta M; Adarmes-Gómez, Astrid Daniela AD; Gómez-Garre, Pilar P; Mir, Pablo P
Publication Date: 2022-09-28

Variant appearance in text: rs1801394
PubMed Link: 36169739
Variant Present in the following documents:
  • Main text
  • 415_2022_Article_11361.pdf
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: MTRR: I22M
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



-Omic Approaches and Treatment Response in Rheumatoid Arthritis.

Pharmaceutics
Madrid-Paredes, Adela A; Martín, Javier J; Márquez, Ana A
Publication Date: 2022-08-08

Variant appearance in text: rs1801394
PubMed Link: 36015273
Variant Present in the following documents:
  • Main text
  • pharmaceutics-14-01648.pdf
View BVdb publication page



A Common Polymorphism in the MTHFD1 Gene Is a Modulator of Risk of Congenital Heart Disease.

Journal Of Cardiovascular Development And Disease
Karas Kuželički, Nataša N; Šmid, Alenka A; Vidmar Golja, Maša M; Kek, Tina T; Geršak, Borut B; Mazič, Uroš U; Mlinarič-Raščan, Irena I; Geršak, Ksenija K
Publication Date: 2022-05-24

Variant appearance in text: rs1801394
PubMed Link: 35735795
Variant Present in the following documents:
  • Main text
  • jcdd-09-00166.pdf
View BVdb publication page



Evaluating the Association Between Genetic Polymorphisms Related to Homocysteine Metabolism and Unexplained Recurrent Pregnancy Loss in Women.

The Application Of Clinical Genetics
Nguyen Ngoc, Nhat N; Tran Ngoc Thao, My M; Trieu Tien, Sang S; Vu Tung, Son S; Le, Hoang H; Ho Sy, Hung H; Nguyen Thanh, Tung T; Trinh The, Son S
Publication Date: 2022

Variant appearance in text: rs1801394
PubMed Link: 35698663
Variant Present in the following documents:
  • Main text
  • tacg-15-55.pdf
View BVdb publication page



Integrated DNA and RNA Sequencing Reveals Drivers of Endocrine Resistance in Estrogen Receptor-Positive Breast Cancer.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Xia, Youli Y; He, Xiaping X; Renshaw, Lorna L; Martinez-Perez, Carlos C; Kay, Charlene C; Gray, Mark M; Meehan, James J; Parker, Joel S JS; Perou, Charles M CM; Carey, Lisa A LA; Dixon, J Michael JM; Turnbull, Arran A
Publication Date: 2022-08-15

Variant appearance in text: rs1801394
PubMed Link: 35653148
Variant Present in the following documents:
  • ccr-21-3189_supplementary_tables_ts1-9_suppts1-9.xlsx, sheet 5
View BVdb publication page



The association between single nucleotide polymorphisms and ovarian cancer risk: A systematic review and network meta-analysis.

Cancer Medicine
Hu, Jia J; Xu, Zhe Z; Ye, Zhuomiao Z; Li, Jin J; Hao, Zhinan Z; Wang, Yongjun Y
Publication Date: 2022-05-30

Variant appearance in text: rs1801394
PubMed Link: 35637613
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pharmacogenetics implementation in the clinics: information and guidelines for germline variants.

Cancer Drug Resistance (Alhambra, Calif.)
Olivera, Gladys G; Sendra, Luis L; Herrero, María José MJ; Berlanga, Pablo P; Gargallo, Pablo P; Yáñez, Yania Y; Urtasun, Andrea A; de Mora, Jaime Font JF; Castel, Victoria V; Cañete, Adela A; Aliño, Salvador F SF
Publication Date: 2019

Variant appearance in text: rs1801394
PubMed Link: 35582138
Variant Present in the following documents:
  • cdr-2-53.pdf
View BVdb publication page



MTRR rs1532268 polymorphism and gastric cancer risk: evidence from a meta-analysis.

The Journal Of International Medical Research
Zhong, Guping G; Luo, Xiaojin X; Li, Ji J; Liao, Yuanhang Y; Gui, Guan G; Sheng, Jianwen J
Publication Date: 2022-05

Variant appearance in text: rs1801394
PubMed Link: 35579185
Variant Present in the following documents:
  • Main text
  • 10.1177_03000605221097486.pdf
View BVdb publication page



Associations of Maternal rs1801131 Genotype in MTHFR and Serum Folate and Vitamin B12 with Gestational Diabetes Mellitus in Chinese Pregnant Women.

Nutrients
Li, Shuying S; Tian, Xiubiao X; Wang, Yiyun Y; Zhang, Xumei X; Zhang, Liwen L; Li, Chen C; Li, Jing J; Wang, Chunhua C; Liu, Huihuan H; Liu, Juan J; Liu, Hongjuan H; Yang, Xueli X; Li, Weiqin W; Leng, Junhong J; Yang, Xilin X; Tang, Naijun N; Zhang, Qiang Q
Publication Date: 2022-03-10

Variant appearance in text: rs1801394
PubMed Link: 35334827
Variant Present in the following documents:
  • Main text
  • nutrients-14-01169.pdf
View BVdb publication page



An Assessment of Selected Molecular and Biochemical Markers of the Folate Pathway as Potential Risk Factors for Fetal Trisomy 21 during the First Trimester of Pregnancy in the Polish Population.

Journal Of Clinical Medicine
Ziółkowska, Katarzyna K; Toboła-Wróbel, Kinga K; Pietryga, Marek M; Kasprzak, Grażyna G; Jamsheer, Aleksander A; Wysocka, Ewa E
Publication Date: 2022-02-23

Variant appearance in text: MTRR: 66A>G; rs1801394
PubMed Link: 35268281
Variant Present in the following documents:
  • Main text
  • jcm-11-01190.pdf
View BVdb publication page



Association of the DNA Methyltransferase and Folate Cycle Enzymes' Gene Polymorphisms with Coronary Restenosis.

Life (Basel, Switzerland)
Timizheva, Kalima B KB; Ahmed, Abdulbary A M AAM; Ait Aissa, Amira A; Aghajanyan, Anna V AV; Tskhovrebova, Leyla V LV; Azova, Madina M MM
Publication Date: 2022-02-07

Variant appearance in text: MTRR: Ile22Met; rs1801394
PubMed Link: 35207533
Variant Present in the following documents:
  • Main text
  • life-12-00245.pdf
View BVdb publication page



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: rs1801394
PubMed Link: 35075162
Variant Present in the following documents:
  • Main text
  • 41598_2021_Article_2159.pdf
View BVdb publication page



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: rs1801394
PubMed Link: 35075162
Variant Present in the following documents:
  • Main text
  • 41598_2021_Article_2159.pdf
View BVdb publication page



Electroencephalogram Signatures of Agitation Induced by Sevoflurane and Its Association With Genetic Polymorphisms.

Frontiers In Medicine
Zhao, Shuai S; Han, Linlin L; Zhou, Ruihui R; Huang, Shiqian S; Wang, Yafeng Y; Xu, Feng F; Shu, Shaofang S; Xia, Leiming L; Chen, Xiangdong X
Publication Date: 2021

Variant appearance in text: rs1801394
PubMed Link: 34917626
Variant Present in the following documents:
  • Main text
  • fmed-08-678185.pdf
View BVdb publication page



Multiomics Landscape Uncovers the Molecular Mechanism of the Malignant Evolution of Lung Adenocarcinoma Cells to Chronic Low Dose Cadmium Exposure.

Frontiers In Oncology
Dai, Shun-Dong SD; Wang, Shuang S; Qin, Ya-Nan YN; Zhu, Jin-Chao JC
Publication Date: 2021

Variant appearance in text: MTRR: I22M
PubMed Link: 34858801
Variant Present in the following documents:
  • Table_1.xls, sheet 1
View BVdb publication page



Universal probe-based intermediate primer-triggered qPCR (UPIP-qPCR) for SNP genotyping.

Bmc Genomics
Li, Baowei B; Liu, Yanran Y; Hao, Xiaodan X; Dong, Jinhua J; Chen, Limei L; Li, Haimei H; Wu, Wei W; Liu, Ying Y; Wang, Jianxun J; Wang, Yin Y; Li, Peifeng P
Publication Date: 2021-11-24

Variant appearance in text: rs1801394
PubMed Link: 34819030
Variant Present in the following documents:
  • Main text
  • 12864_2021_Article_8148.pdf
View BVdb publication page



Understanding etiology of chromosome 21 nondisjunction from gene × environment models.

Scientific Reports
Halder, Pinku P; Pal, Upamanyu U; Ganguly, Agnish A; Ghosh, Papiya P; Ray, Anirban A; Sarkar, Sumantra S; Ghosh, Sujay S
Publication Date: 2021-11-17

Variant appearance in text: rs1801394
PubMed Link: 34789805
Variant Present in the following documents:
  • Main text
View BVdb publication page



Understanding etiology of chromosome 21 nondisjunction from gene × environment models.

Scientific Reports
Halder, Pinku P; Pal, Upamanyu U; Ganguly, Agnish A; Ghosh, Papiya P; Ray, Anirban A; Sarkar, Sumantra S; Ghosh, Sujay S
Publication Date: 2021-11-17

Variant appearance in text: rs1801394
PubMed Link: 34789805
Variant Present in the following documents:
  • Main text
View BVdb publication page



Combining genetic risk score with artificial neural network to predict the efficacy of folic acid therapy to hyperhomocysteinemia.

Scientific Reports
Chen, Xiaorui X; Huang, Xiaowen X; Jie, Diao D; Zheng, Caifang C; Wang, Xiliang X; Zhang, Bowen B; Shao, Weihao W; Wang, Gaili G; Zhang, Weidong W
Publication Date: 2021-11-02

Variant appearance in text: rs1801394
PubMed Link: 34728708
Variant Present in the following documents:
  • Main text
View BVdb publication page