Using the optimal method—explained variance weighted genetic risk score to predict the efficacy of folic acid therapy to hyperhomocysteinemia
Background Genetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single nucleotide polymorphisms (SNPs) associated with the efficacy of folic acid treatment to hyperhomocysteinemia (HHcy). Methods We aim...
Saved in:
Published in | European journal of clinical nutrition Vol. 76; no. 7; pp. 943 - 949 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.07.2022
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Background
Genetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single nucleotide polymorphisms (SNPs) associated with the efficacy of folic acid treatment to hyperhomocysteinemia (HHcy).
Methods
We aimed to construct and screen out the optimal predictive model based on four GRSs and traditional risk factors. Four GRSs enrolled four SNPs (
MTHFR rs1801131, MTHFR rs1801133, MTRR rs1801394, BHMT rs3733890
) were presented as follows: (a) simple count genetic risk score (SC-GRS), (b) direct logistic regression genetic risk score (DL-GRS), (c) polygenic genetic risk score (PG-GRS), and (d) explained variance weighted genetic risk score (EV-GRS). We performed a prospective cohort study including 638 HHcy patients. Then we evaluated the associations of four GRSs with folic acid’s efficacy and the performance of four GRSs.
Results
Four GRSs were independently associated with efficacy of treatment (
p
< 0.05). When combining GRSs with traditional risk factors, the AUC of the four models were all above 0.900 in the training set (Tradition + SC-GRS: 0.909, Tradition + DL-GRS: 0.909, Tradition + PG-GRS: 0.904, Tradition + EV-GRS: 0.910). And EV-GRS got the highest AUC. When evaluating the models in the testing set, we got the same conclusion that EV-GRS was optimal among four GRSs with the highest AUC (0.878) and the highest increase of AUC (0.008).
Conclusion
A more precise predictive model combing the optimal GRS with traditional risk factors was constructed to predict the efficacy of folic acid therapy to HHcy. |
---|---|
AbstractList | Genetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single nucleotide polymorphisms (SNPs) associated with the efficacy of folic acid treatment to hyperhomocysteinemia (HHcy).
We aimed to construct and screen out the optimal predictive model based on four GRSs and traditional risk factors. Four GRSs enrolled four SNPs (MTHFR rs1801131, MTHFR rs1801133, MTRR rs1801394, BHMT rs3733890) were presented as follows: (a) simple count genetic risk score (SC-GRS), (b) direct logistic regression genetic risk score (DL-GRS), (c) polygenic genetic risk score (PG-GRS), and (d) explained variance weighted genetic risk score (EV-GRS). We performed a prospective cohort study including 638 HHcy patients. Then we evaluated the associations of four GRSs with folic acid's efficacy and the performance of four GRSs.
Four GRSs were independently associated with efficacy of treatment (p < 0.05). When combining GRSs with traditional risk factors, the AUC of the four models were all above 0.900 in the training set (Tradition + SC-GRS: 0.909, Tradition + DL-GRS: 0.909, Tradition + PG-GRS: 0.904, Tradition + EV-GRS: 0.910). And EV-GRS got the highest AUC. When evaluating the models in the testing set, we got the same conclusion that EV-GRS was optimal among four GRSs with the highest AUC (0.878) and the highest increase of AUC (0.008).
A more precise predictive model combing the optimal GRS with traditional risk factors was constructed to predict the efficacy of folic acid therapy to HHcy. Genetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single nucleotide polymorphisms (SNPs) associated with the efficacy of folic acid treatment to hyperhomocysteinemia (HHcy).BACKGROUNDGenetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single nucleotide polymorphisms (SNPs) associated with the efficacy of folic acid treatment to hyperhomocysteinemia (HHcy).We aimed to construct and screen out the optimal predictive model based on four GRSs and traditional risk factors. Four GRSs enrolled four SNPs (MTHFR rs1801131, MTHFR rs1801133, MTRR rs1801394, BHMT rs3733890) were presented as follows: (a) simple count genetic risk score (SC-GRS), (b) direct logistic regression genetic risk score (DL-GRS), (c) polygenic genetic risk score (PG-GRS), and (d) explained variance weighted genetic risk score (EV-GRS). We performed a prospective cohort study including 638 HHcy patients. Then we evaluated the associations of four GRSs with folic acid's efficacy and the performance of four GRSs.METHODSWe aimed to construct and screen out the optimal predictive model based on four GRSs and traditional risk factors. Four GRSs enrolled four SNPs (MTHFR rs1801131, MTHFR rs1801133, MTRR rs1801394, BHMT rs3733890) were presented as follows: (a) simple count genetic risk score (SC-GRS), (b) direct logistic regression genetic risk score (DL-GRS), (c) polygenic genetic risk score (PG-GRS), and (d) explained variance weighted genetic risk score (EV-GRS). We performed a prospective cohort study including 638 HHcy patients. Then we evaluated the associations of four GRSs with folic acid's efficacy and the performance of four GRSs.Four GRSs were independently associated with efficacy of treatment (p < 0.05). When combining GRSs with traditional risk factors, the AUC of the four models were all above 0.900 in the training set (Tradition + SC-GRS: 0.909, Tradition + DL-GRS: 0.909, Tradition + PG-GRS: 0.904, Tradition + EV-GRS: 0.910). And EV-GRS got the highest AUC. When evaluating the models in the testing set, we got the same conclusion that EV-GRS was optimal among four GRSs with the highest AUC (0.878) and the highest increase of AUC (0.008).RESULTSFour GRSs were independently associated with efficacy of treatment (p < 0.05). When combining GRSs with traditional risk factors, the AUC of the four models were all above 0.900 in the training set (Tradition + SC-GRS: 0.909, Tradition + DL-GRS: 0.909, Tradition + PG-GRS: 0.904, Tradition + EV-GRS: 0.910). And EV-GRS got the highest AUC. When evaluating the models in the testing set, we got the same conclusion that EV-GRS was optimal among four GRSs with the highest AUC (0.878) and the highest increase of AUC (0.008).A more precise predictive model combing the optimal GRS with traditional risk factors was constructed to predict the efficacy of folic acid therapy to HHcy.CONCLUSIONA more precise predictive model combing the optimal GRS with traditional risk factors was constructed to predict the efficacy of folic acid therapy to HHcy. BackgroundGenetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single nucleotide polymorphisms (SNPs) associated with the efficacy of folic acid treatment to hyperhomocysteinemia (HHcy).MethodsWe aimed to construct and screen out the optimal predictive model based on four GRSs and traditional risk factors. Four GRSs enrolled four SNPs (MTHFR rs1801131, MTHFR rs1801133, MTRR rs1801394, BHMT rs3733890) were presented as follows: (a) simple count genetic risk score (SC-GRS), (b) direct logistic regression genetic risk score (DL-GRS), (c) polygenic genetic risk score (PG-GRS), and (d) explained variance weighted genetic risk score (EV-GRS). We performed a prospective cohort study including 638 HHcy patients. Then we evaluated the associations of four GRSs with folic acid’s efficacy and the performance of four GRSs.ResultsFour GRSs were independently associated with efficacy of treatment (p < 0.05). When combining GRSs with traditional risk factors, the AUC of the four models were all above 0.900 in the training set (Tradition + SC-GRS: 0.909, Tradition + DL-GRS: 0.909, Tradition + PG-GRS: 0.904, Tradition + EV-GRS: 0.910). And EV-GRS got the highest AUC. When evaluating the models in the testing set, we got the same conclusion that EV-GRS was optimal among four GRSs with the highest AUC (0.878) and the highest increase of AUC (0.008).ConclusionA more precise predictive model combing the optimal GRS with traditional risk factors was constructed to predict the efficacy of folic acid therapy to HHcy. Background Genetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single nucleotide polymorphisms (SNPs) associated with the efficacy of folic acid treatment to hyperhomocysteinemia (HHcy). Methods We aimed to construct and screen out the optimal predictive model based on four GRSs and traditional risk factors. Four GRSs enrolled four SNPs ( MTHFR rs1801131, MTHFR rs1801133, MTRR rs1801394, BHMT rs3733890 ) were presented as follows: (a) simple count genetic risk score (SC-GRS), (b) direct logistic regression genetic risk score (DL-GRS), (c) polygenic genetic risk score (PG-GRS), and (d) explained variance weighted genetic risk score (EV-GRS). We performed a prospective cohort study including 638 HHcy patients. Then we evaluated the associations of four GRSs with folic acid’s efficacy and the performance of four GRSs. Results Four GRSs were independently associated with efficacy of treatment ( p < 0.05). When combining GRSs with traditional risk factors, the AUC of the four models were all above 0.900 in the training set (Tradition + SC-GRS: 0.909, Tradition + DL-GRS: 0.909, Tradition + PG-GRS: 0.904, Tradition + EV-GRS: 0.910). And EV-GRS got the highest AUC. When evaluating the models in the testing set, we got the same conclusion that EV-GRS was optimal among four GRSs with the highest AUC (0.878) and the highest increase of AUC (0.008). Conclusion A more precise predictive model combing the optimal GRS with traditional risk factors was constructed to predict the efficacy of folic acid therapy to HHcy. |
Author | Wang, Xiliang Huang, Xiaowen Chen, Xiaorui Zheng, Caifang Zhang, Weidong |
Author_xml | – sequence: 1 givenname: Xiaorui surname: Chen fullname: Chen, Xiaorui organization: Department of Epidemiology, School of Public Health, Zhengzhou University – sequence: 2 givenname: Xiaowen surname: Huang fullname: Huang, Xiaowen organization: Department of Epidemiology, School of Public Health, Zhengzhou University – sequence: 3 givenname: Caifang surname: Zheng fullname: Zheng, Caifang organization: Department of Epidemiology, School of Public Health, Zhengzhou University – sequence: 4 givenname: Xiliang surname: Wang fullname: Wang, Xiliang organization: Department of Epidemiology, School of Public Health, Zhengzhou University – sequence: 5 givenname: Weidong orcidid: 0000-0002-0314-7820 surname: Zhang fullname: Zhang, Weidong email: imooni@163.com organization: Department of Epidemiology, School of Public Health, Zhengzhou University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35001080$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kc1u1DAUhS1URKeFF2CBLLFhk3Id_yRZooqfSpXY0HXkn5sZlyQOtgfIjjdgwxPyJHg6BSQWrGz5fuce65wzcjKHGQl5yuCCAW9fJsEEhwpqVgEDKSv5gGyYaFQllYATsoFOiooDNKfkLKVbgDJs6kfklMtyhxY25PtN8vOW5h3SsGQ_6ZFOmHfB_fz2A78uo_YzOvpZR69ni_QL-u0ul5ctzpi9pdGnjzTZEJHmQJeIztt8tw6HwVttVxoGOoSxsNp6dxhFvawHercuGHdhCnZNGYvR5PVj8nDQY8In9-c5uXnz-sPlu-r6_dury1fXleW1ypUVjkFttbPGyrarWSMacKbpEGTDpTNGdLxrFW-0MY53phuMUM7UCriQ3cDPyYvj3iWGT3tMuZ98sjiOesawT32tWCvhEHNBn_-D3oZ9nMvvCtUqUSspVKGe3VN7M6Hrl1jCjGv_O-oC1EfAxpBSxOEPwqA_GPXHPvvSZ3_XZy-LiB9FqcDzFuNf7_-ofgEkc6T_ |
Cites_doi | 10.1006/mgme.2000.2993 10.1111/j.1464-5491.2011.03438.x 10.1080/07315724.2017.1330162 10.1093/bib/bby075 10.1002/sim.4006 10.1161/CIRCULATIONAHA.119.043805 10.1038/s41588-019-0487-7 10.1038/sj.ejcn.1602897 10.1161/01.ATV.17.6.1157 10.1631/jzus.B1400183 10.1038/s10038-019-0672-7 10.3748/wjg.v22.i14.3777 10.1136/gut.47.3.456 10.1111/1755-5922.12014 10.1002/ijc.32272 10.1016/j.gene.2013.06.041 10.1016/S0140-6736(10)61267-6 10.1017/S0007114518002477 10.3390/nu5051531 10.1515/1544-6115.1796 10.1038/ng.3368 10.1038/ejhg.2014.212 10.1136/bmj.b4838 10.1016/j.nut.2004.08.004 10.1017/S0007114519000783 10.1007/s11892-017-0961-5 10.1016/j.thromres.2014.05.025 10.1093/ije/dyu132 10.1017/S0007114518000508 10.1007/s00774-018-0920-5 10.1097/MD.0000000000002652 10.1371/journal.pgen.1003348 10.3390/nu12071957 10.1161/CIRCULATIONAHA.116.024436 10.1161/ATVBAHA.117.310211 10.1002/gepi.21762 10.1001/archneur.55.11.1449 10.1038/s41430-020-0657-9 |
ContentType | Journal Article |
Copyright | The Author(s), under exclusive licence to Springer Nature Limited 2021 2021. The Author(s), under exclusive licence to Springer Nature Limited. The Author(s), under exclusive licence to Springer Nature Limited 2021. |
Copyright_xml | – notice: The Author(s), under exclusive licence to Springer Nature Limited 2021 – notice: 2021. The Author(s), under exclusive licence to Springer Nature Limited. – notice: The Author(s), under exclusive licence to Springer Nature Limited 2021. |
DBID | AAYXX CITATION NPM 3V. 7QP 7RV 7TK 7X2 7X7 7XB 88E 8AO 8C1 8FE 8FH 8FI 8FJ 8FK 8G5 ABUWG AEUYN AFKRA AN0 ATCPS AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FYUFA GHDGH GNUQQ GUQSH HCIFZ K9. KB0 LK8 M0K M0S M1P M2O M7P MBDVC NAPCQ PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS Q9U 7X8 |
DOI | 10.1038/s41430-021-01055-5 |
DatabaseName | CrossRef PubMed ProQuest Central (Corporate) Calcium & Calcified Tissue Abstracts Nursing & Allied Health Database Neurosciences Abstracts Agricultural Science Collection Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) ProQuest Pharma Collection Public Health Database ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Research Library ProQuest Central (Alumni) ProQuest One Sustainability ProQuest Central UK/Ireland British Nursing Database (Proquest) Agricultural & Environmental Science Collection ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection ProQuest One Community College ProQuest Central Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student ProQuest Research Library SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Database (Alumni Edition) Biological Sciences Agricultural Science Database ProQuest Health & Medical Collection Medical Database ProQuest Research Library Biological Science Database Research Library (Corporate) Nursing & Allied Health Premium ProQuest Central Premium ProQuest One Academic ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest Central Basic MEDLINE - Academic |
DatabaseTitle | CrossRef PubMed Agricultural Science Database Research Library Prep ProQuest Central Student ProQuest Central Essentials SciTech Premium Collection ProQuest Central China ProQuest One Applied & Life Sciences ProQuest One Sustainability Health Research Premium Collection Natural Science Collection Health & Medical Research Collection Biological Science Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Biological Science Collection ProQuest One Academic Eastern Edition Agricultural Science Collection ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database Neurosciences Abstracts ProQuest Hospital Collection (Alumni) Nursing & Allied Health Premium ProQuest Health & Medical Complete ProQuest One Academic UKI Edition ProQuest Nursing & Allied Health Source (Alumni) ProQuest One Academic Calcium & Calcified Tissue Abstracts ProQuest One Academic (New) ProQuest One Academic Middle East (New) ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing Research Library (Alumni Edition) ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central ProQuest Health & Medical Research Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Agricultural & Environmental Science Collection ProQuest Research Library ProQuest Public Health ProQuest Central Basic British Nursing Index with Full Text ProQuest Nursing & Allied Health Source ProQuest SciTech Collection ProQuest Medical Library ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic Agricultural Science Database |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Public Health Anatomy & Physiology Diet & Clinical Nutrition |
EISSN | 1476-5640 |
EndPage | 949 |
ExternalDocumentID | 35001080 10_1038_s41430_021_01055_5 |
Genre | Journal Article |
GrantInformation_xml | – fundername: Science and Technology Department of Henan Province (Henan Provincial Department of Science and Technology) grantid: 132102310431 funderid: https://doi.org/10.13039/501100011447 – fundername: Science and Technology Department of Henan Province (Henan Provincial Department of Science and Technology) grantid: 132102310431 |
GroupedDBID | --- -ET -Q- .GJ 0R~ 29G 2WC 36B 39C 4.4 406 53G 5GY 5RE 6PF 70F 7RV 7X2 7X7 88E 8AO 8C1 8FE 8FH 8FI 8FJ 8G5 8R4 8R5 A8Z AACDK AAHBH AAIKC AAMNW AANZL AASML AATNV AAWTL AAYZH ABAKF ABAWZ ABBRH ABCQX ABDBE ABDBF ABFSG ABJNI ABLJU ABOCM ABRTQ ABUWG ABZZP ACAOD ACGFO ACGFS ACKTT ACMJI ACPRK ACRQY ACSTC ACUHS ACZOJ ADBBV ADFRT ADHUB AEFQL AEJRE AEMSY AENEX AEUYN AEVLU AEXYK AEZWR AFBBN AFDZB AFHIU AFKRA AFRAH AFSHS AGAYW AGHAI AGQEE AHMBA AHSBF AHWEU AI. AIGIU AILAN AIXLP AJRNO ALFFA ALIPV ALMA_UNASSIGNED_HOLDINGS AMYLF AN0 APEBS ATCPS ATHPR AXYYD AYFIA AZQEC B0M BAWUL BBNVY BENPR BHPHI BKEYQ BKKNO BKOMP BNQBC BPHCQ BVXVI CCPQU CS3 DIK DNIVK DPUIP DU5 DWQXO E.L E3Z EAD EAP EAS EBC EBD EBLON EBO EBS ECGQY EE. EHN EIHBH EIOEI EJD EMB EMK EMOBN EPL EPT ESX EX3 F5P FDQFY FERAY FIGPU FIZPM FSGXE FYUFA GNUQQ GUQSH HCIFZ HMCUK HZ~ IAG IAO ICU IEA IHR IHT IHW INH INR IOF ITC IWAJR JSO JZLTJ KQ8 LGEZI LOTEE M0K M1P M2O M7P NADUK NAPCQ NQJWS NXXTH O9- OK1 OVD P2P PHGZM PHGZT PJZUB PPXIY PQGLB PQQKQ PROAC PSQYO Q2X Q~Q RNS RNT RNTTT ROL RXW SNX SNYQT SOHCF SOJ SRMVM SV3 SWTZT TAE TAOOD TBHMF TDRGL TEORI TH9 TR2 TSG TUS UKHRP VH1 WH7 WOW XOL ZXP ~02 ~8M ~KM AAYXX ACMFV CITATION NPM 3V. 7QP 7TK 7XB 8FK K9. LK8 MBDVC PKEHL PQEST PQUKI PRINS Q9U 7X8 |
ID | FETCH-LOGICAL-c326t-c4d102cadcbc589217470db79e05735dbb49398637abbd39b9fb46db2603459f3 |
IEDL.DBID | 7X7 |
ISSN | 0954-3007 1476-5640 |
IngestDate | Mon Jul 21 09:45:48 EDT 2025 Sat Aug 16 21:44:49 EDT 2025 Thu Apr 03 07:07:15 EDT 2025 Tue Jul 01 03:15:31 EDT 2025 Mon Jul 21 06:07:00 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 7 |
Language | English |
License | 2021. The Author(s), under exclusive licence to Springer Nature Limited. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c326t-c4d102cadcbc589217470db79e05735dbb49398637abbd39b9fb46db2603459f3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-0314-7820 |
PMID | 35001080 |
PQID | 2686426546 |
PQPubID | 33883 |
PageCount | 7 |
ParticipantIDs | proquest_miscellaneous_2618501038 proquest_journals_2686426546 pubmed_primary_35001080 crossref_primary_10_1038_s41430_021_01055_5 springer_journals_10_1038_s41430_021_01055_5 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2022-07-01 |
PublicationDateYYYYMMDD | 2022-07-01 |
PublicationDate_xml | – month: 07 year: 2022 text: 2022-07-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | London |
PublicationPlace_xml | – name: London – name: England |
PublicationTitle | European journal of clinical nutrition |
PublicationTitleAbbrev | Eur J Clin Nutr |
PublicationTitleAlternate | Eur J Clin Nutr |
PublicationYear | 2022 |
Publisher | Nature Publishing Group UK Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
References | Zappacosta, Mastroiacovo, Persichilli, Pounis, Ruggeri, Minucci (CR13) 2013; 5 Liu, Chiang, Chen (CR25) 2004; 20 Hernandez, Uricchio, Hartman, Ye, Dahl, Zaitlen (CR35) 2019; 51 Ohishi, Fujita, Suzuki, Nishida, Asukai, Matsuyama (CR1) 2019; 37 Tian, Tian, Zhang, Wang, Wang, Ge (CR11) 2017; 36 Redondo, Oram, Steck (CR39) 2017; 17 Talmud, Hingorani, Cooper, Marmot, Brunner, Kumari (CR22) 2010; 340 Natarajan, Young, Stitziel, Padmanabhan, Baber, Mehran (CR20) 2017; 135 Sidore, Busonero, Maschio, Porcu, Naitza, Zoledziewska (CR36) 2015; 47 Huang, Zhao, Li, Ren, Yue, Shi (CR16) 2020; 74 Dhonukshe-Rutten, de Vries, de Bree, van der Put, van Staveren, de Groot (CR7) 2009; 63 Du, Zhang, Yue, Ren, Zhao, Li (CR18) 2019; 122 Huang, Li, Zhao, Zhang, Ren, Yue (CR15) 2019; 64 Wu, Pfeiffer, Gail (CR31) 2013; 37 Tian, Tian, Zhang, Wang, Wang, Ge (CR14) 2017; 36 Clarke, Smith, Jobst, Refsum, Sutton, Ueland (CR6) 1998; 55 Balavarca, Weigl, Thomsen, Brenner (CR34) 2020; 146 Zupancic, Skok, Repnik, Weersma, Potocnik, Skok (CR38) 2016; 22 Huang, Qin, Yang, Liu, Jiang, Zhang (CR26) 2018; 38 Mahmud, Molloy, McPartlin, Corbally, Whitehead, Scott, Weir (CR8) 2000; 47 Ripatti, Tikkanen, Orho-Melander, Havulinna, Silander, Sharma (CR30) 2010; 376 Dudbridge (CR32) 2013; 9 Janipalli, Kumar, Vinay, Sandeep, Bhaskar, Kulkarni (CR29) 2012; 29 Wang, Yan, Xu, Li, Cheng (CR33) 2019; 32 Vezzoli, Dellanoce, Maria Caimi, Vietti, Montorsi, Mrakic-Sposta (CR40) 2020; 12 Carayol, Tores, Konig, Hager, Ziegler (CR23) 2010; 29 Che, Motsinger-Reif (CR24) 2012; 11 Kruger, Evans, Wang, Malinow, Duell, Anderson (CR27) 2000; 70 Marston, Kamanu, Nordio, Gurmu, Roselli, Sever (CR21) 2020; 141 Zhao, Ning, Zhang, Ding, Wen, Shi (CR19) 2019; 20 Mao, Xing, Xu, Gong, He, Li (CR12) 2016; 95 Malinow, Nieto, Kruger, Duell, Hess, Gluckman (CR28) 1997; 17 Cheng (CR5) 2013; 31 Fava, Sjogren, Olsson, Lovkvist, Jood, Engstrom (CR37) 2015; 23 Wang, Wu, Li, Ban, Huang, Chen (CR10) 2018; 120 Peng, Man, Xu, Fan (CR3) 2015; 16 Du, Tian, Tian, Zhang, Wang, Wang (CR17) 2018; 119 Messedi, Frigui, Chaabouni, Turki, Neifer, Lahiyani (CR2) 2013; 527 Schaffer, Verdoia, Cassetti, Marino, Suryapranata, De Luca (CR4) 2014; 134 Yajnik, Chandak, Joglekar, Katre, Bhat, Singh (CR9) 2014; 43 A Vezzoli (1055_CR40) 2020; 12 X Huang (1055_CR16) 2020; 74 WD Kruger (1055_CR27) 2000; 70 RA Dhonukshe-Rutten (1055_CR7) 2009; 63 A Schaffer (1055_CR4) 2014; 134 J Carayol (1055_CR23) 2010; 29 M Messedi (1055_CR2) 2013; 527 F Dudbridge (1055_CR32) 2013; 9 B Zappacosta (1055_CR13) 2013; 5 CS Yajnik (1055_CR9) 2014; 43 CS Liu (1055_CR25) 2004; 20 X Cheng (1055_CR5) 2013; 31 B Wang (1055_CR10) 2018; 120 HY Peng (1055_CR3) 2015; 16 M Malinow (1055_CR28) 1997; 17 B Du (1055_CR18) 2019; 122 P Natarajan (1055_CR20) 2017; 135 PJ Talmud (1055_CR22) 2010; 340 X Huang (1055_CR15) 2019; 64 K Zupancic (1055_CR38) 2016; 22 H Tian (1055_CR14) 2017; 36 B Du (1055_CR17) 2018; 119 RD Hernandez (1055_CR35) 2019; 51 C Janipalli (1055_CR29) 2012; 29 C Fava (1055_CR37) 2015; 23 Y Zhao (1055_CR19) 2019; 20 J Wu (1055_CR31) 2013; 37 NA Marston (1055_CR21) 2020; 141 N Mahmud (1055_CR8) 2000; 47 R Che (1055_CR24) 2012; 11 X Huang (1055_CR26) 2018; 38 X Mao (1055_CR12) 2016; 95 H Tian (1055_CR11) 2017; 36 S Ripatti (1055_CR30) 2010; 376 MJ Redondo (1055_CR39) 2017; 17 Y Wang (1055_CR33) 2019; 32 R Clarke (1055_CR6) 1998; 55 C Sidore (1055_CR36) 2015; 47 Y Balavarca (1055_CR34) 2020; 146 T Ohishi (1055_CR1) 2019; 37 |
References_xml | – volume: 70 start-page: 53 year: 2000 end-page: 60 ident: CR27 article-title: Polymorphisms in the CBS gene associated with decreased risk of coronary artery disease and increased responsiveness to total homocysteine lowering by folic acid publication-title: Mol Genet Metab doi: 10.1006/mgme.2000.2993 – volume: 29 start-page: 121 year: 2012 end-page: 7 ident: CR29 article-title: Analysis of 32 common susceptibility genetic variants and their combined effect in predicting risk of Type 2 diabetes and related traits in Indians publication-title: Diabet Med doi: 10.1111/j.1464-5491.2011.03438.x – volume: 36 start-page: 528 year: 2017 end-page: 32 ident: CR11 article-title: Efficacy of folic acid therapy in patients with hyperhomocysteinemia publication-title: J Am Coll Nutr doi: 10.1080/07315724.2017.1330162 – volume: 20 start-page: 2291 year: 2019 end-page: 8 ident: CR19 article-title: PCA-based GRS analysis enhances the effectiveness for genetic correlation detection publication-title: Brief Bioinform doi: 10.1093/bib/bby075 – volume: 29 start-page: 2359 year: 2010 end-page: 68 ident: CR23 article-title: Evaluating diagnostic accuracy of genetic profiles in affected offspring families publication-title: Stat Med doi: 10.1002/sim.4006 – volume: 141 start-page: 616 year: 2020 end-page: 23 ident: CR21 article-title: Predicting benefit from evolocumab therapy in patients with atherosclerotic disease using a genetic risk score: results from the FOURIER trial publication-title: Circulation. doi: 10.1161/CIRCULATIONAHA.119.043805 – volume: 51 start-page: 1349 year: 2019 end-page: 55 ident: CR35 article-title: Ultrarare variants drive substantial cis heritability of human gene expression publication-title: Nat Genet doi: 10.1038/s41588-019-0487-7 – volume: 63 start-page: 18 year: 2009 end-page: 30 ident: CR7 article-title: Dietary intake and status of folate and vitamin B12 and their association with homocysteine and cardiovascular disease in European populations publication-title: Eur J Clin Nutr doi: 10.1038/sj.ejcn.1602897 – volume: 17 start-page: 1157 year: 1997 end-page: 62 ident: CR28 article-title: The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes publication-title: Arterioscler Thromb Vasc Biol doi: 10.1161/01.ATV.17.6.1157 – volume: 16 start-page: 78 year: 2015 end-page: 86 ident: CR3 article-title: Elevated homocysteine levels and risk of cardiovascular and all-cause mortality: a meta-analysis of prospective studies publication-title: J Zhejiang Univ Sci B. doi: 10.1631/jzus.B1400183 – volume: 64 start-page: 1227 year: 2019 end-page: 35 ident: CR15 article-title: Association between BHMT and CBS gene promoter methylation with the efficacy of folic acid therapy in patients with hyperhomocysteinemia publication-title: J Hum Genet doi: 10.1038/s10038-019-0672-7 – volume: 22 start-page: 3777 year: 2016 end-page: 84 ident: CR38 article-title: Multi-locus genetic risk score predicts risk for Crohn’s disease in Slovenian population publication-title: World J Gastroenterol doi: 10.3748/wjg.v22.i14.3777 – volume: 47 start-page: 456 year: 2000 end-page: 457 ident: CR8 article-title: Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications publication-title: Gut doi: 10.1136/gut.47.3.456 – volume: 31 start-page: e19 year: 2013 end-page: 26 ident: CR5 article-title: Updating the relationship between hyperhomocysteinemia lowering therapy and cardiovascular events publication-title: Cardiovasc Ther doi: 10.1111/1755-5922.12014 – volume: 146 start-page: 627 year: 2020 end-page: 34 ident: CR34 article-title: Performance of individual and joint risk stratification by an environmental risk score and a genetic risk score in a colorectal cancer screening setting publication-title: Int J Cancer doi: 10.1002/ijc.32272 – volume: 527 start-page: 306 year: 2013 end-page: 10 ident: CR2 article-title: Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and variations of homocysteine concentrations in patients with Behcet’s disease publication-title: Gene. doi: 10.1016/j.gene.2013.06.041 – volume: 376 start-page: 1393 year: 2010 end-page: 400 ident: CR30 article-title: A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses publication-title: Lancet doi: 10.1016/S0140-6736(10)61267-6 – volume: 120 start-page: 1122 year: 2018 end-page: 30 ident: CR10 article-title: Effect of long-term low-dose folic acid supplementation on degree of total homocysteine-lowering: major effect modifiers publication-title: Br J Nutr doi: 10.1017/S0007114518002477 – volume: 5 start-page: 1531 year: 2013 end-page: 43 ident: CR13 article-title: Homocysteine lowering by folate-rich diet or pharmacological supplementations in subjects with moderate hyperhomocysteinemia publication-title: Nutrients. doi: 10.3390/nu5051531 – volume: 11 start-page: Article 15 year: 2012 ident: CR24 article-title: A new explained-variance based genetic risk score for predictive modeling of disease risk publication-title: Stat Appl Genet Mol Biol doi: 10.1515/1544-6115.1796 – volume: 47 start-page: 1272 year: 2015 end-page: 81 ident: CR36 article-title: Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers publication-title: Nat Genet doi: 10.1038/ng.3368 – volume: 23 start-page: 969 year: 2015 end-page: 74 ident: CR37 article-title: A genetic risk score for hypertension associates with the risk of ischemic stroke in a Swedish case-control study publication-title: Eur J Hum Genet doi: 10.1038/ejhg.2014.212 – volume: 340 start-page: b4838 year: 2010 ident: CR22 article-title: Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: whitehall II prospective cohort study publication-title: BMJ doi: 10.1136/bmj.b4838 – volume: 20 start-page: 974 year: 2004 end-page: 8 ident: CR25 article-title: Methylenetetrahydrofolate reductase polymorphism determines the plasma homocysteine-lowering effect of large-dose folic acid supplementation in patients with cardiovascular disease publication-title: Nutrition. doi: 10.1016/j.nut.2004.08.004 – volume: 122 start-page: 39 year: 2019 end-page: 46 ident: CR18 article-title: Prediction model for the efficacy of folic acid therapy on hyperhomocysteinaemia based on genetic risk score methods publication-title: Br J Nutr doi: 10.1017/S0007114519000783 – volume: 17 start-page: 129. year: 2017 ident: CR39 article-title: Genetic risk scores for type 1 diabetes prediction and diagnosis publication-title: Curr Diabetes Rep doi: 10.1007/s11892-017-0961-5 – volume: 134 start-page: 288 year: 2014 end-page: 93 ident: CR4 article-title: Relationship between homocysteine and coronary artery disease. results from a large prospective cohort study publication-title: Thromb Res doi: 10.1016/j.thromres.2014.05.025 – volume: 32 start-page: 63 year: 2019 end-page: 7 ident: CR33 article-title: High prevalence and factors contributing to hyperhomocysteinemia, folate deficiency, and vitamin b12 deficiency among healthy adults in Shanghai, China publication-title: Biomed Environ Sci – volume: 43 start-page: 1487 year: 2014 end-page: 97 ident: CR9 article-title: Maternal homocysteine in pregnancy and offspring birthweight: epidemiological associations and Mendelian randomization analysis publication-title: Int J Epidemiol doi: 10.1093/ije/dyu132 – volume: 119 start-page: 887 year: 2018 end-page: 95 ident: CR17 article-title: Genetic polymorphisms of key enzymes in folate metabolism affect the efficacy of folate therapy in patients with hyperhomocysteinaemia publication-title: Br J Nutr doi: 10.1017/S0007114518000508 – volume: 37 start-page: 319 year: 2019 end-page: 26 ident: CR1 article-title: Serum homocysteine levels are affected by renal function during a 3-year period of minodronate therapy in female osteoporotic patients publication-title: J Bone Miner Metab doi: 10.1007/s00774-018-0920-5 – volume: 95 start-page: e2652 year: 2016 ident: CR12 article-title: Folic acid and vitamins D and B12 correlate with homocysteine in Chinese patients with type-2 diabetes mellitus, hypertension, or cardiovascular disease publication-title: Medicine doi: 10.1097/MD.0000000000002652 – volume: 9 start-page: e1003348 year: 2013 ident: CR32 article-title: Power and predictive accuracy of polygenic risk scores publication-title: PLoS Genet doi: 10.1371/journal.pgen.1003348 – volume: 12 start-page: 1957 year: 2020 ident: CR40 article-title: Influence of dietary supplementation for hyperhomocysteinemia treatments publication-title: Nutrients. doi: 10.3390/nu12071957 – volume: 36 start-page: 528 year: 2017 end-page: 32 ident: CR14 article-title: Efficacy of folic acid therapy in patients with hyperhomocysteinemia publication-title: J Am Coll Nutr doi: 10.1080/07315724.2017.1330162 – volume: 135 start-page: 2091 year: 2017 end-page: 101 ident: CR20 article-title: Polygenic risk score identifies subgroup with higher burden of atherosclerosis and greater relative benefit from statin therapy in the primary prevention setting publication-title: Circulation. doi: 10.1161/CIRCULATIONAHA.116.024436 – volume: 38 start-page: 679 year: 2018 end-page: 85 ident: CR26 article-title: MTHFR gene and serum folate interaction on serum homocysteine lowering: prospect for precision folic acid treatment publication-title: Arterioscler Thromb Vasc Biol doi: 10.1161/ATVBAHA.117.310211 – volume: 37 start-page: 768 year: 2013 end-page: 77 ident: CR31 article-title: Strategies for developing prediction models from genome-wide association studies publication-title: Genet Epidemiol doi: 10.1002/gepi.21762 – volume: 55 start-page: 1449 year: 1998 end-page: 55 ident: CR6 article-title: Folate, vitamin B12, and serum total homocysteine levels in confirmed Alzheimer disease publication-title: Arch Neurol doi: 10.1001/archneur.55.11.1449 – volume: 74 start-page: 1677 year: 2020 end-page: 84 ident: CR16 article-title: Association between gene promoter methylation of the one-carbon metabolism pathway and serum folate among patients with hyperhomocysteinemia publication-title: Eur J Clin Nutr doi: 10.1038/s41430-020-0657-9 – volume: 55 start-page: 1449 year: 1998 ident: 1055_CR6 publication-title: Arch Neurol doi: 10.1001/archneur.55.11.1449 – volume: 122 start-page: 39 year: 2019 ident: 1055_CR18 publication-title: Br J Nutr doi: 10.1017/S0007114519000783 – volume: 9 start-page: e1003348 year: 2013 ident: 1055_CR32 publication-title: PLoS Genet doi: 10.1371/journal.pgen.1003348 – volume: 5 start-page: 1531 year: 2013 ident: 1055_CR13 publication-title: Nutrients. doi: 10.3390/nu5051531 – volume: 29 start-page: 121 year: 2012 ident: 1055_CR29 publication-title: Diabet Med doi: 10.1111/j.1464-5491.2011.03438.x – volume: 376 start-page: 1393 year: 2010 ident: 1055_CR30 publication-title: Lancet doi: 10.1016/S0140-6736(10)61267-6 – volume: 20 start-page: 974 year: 2004 ident: 1055_CR25 publication-title: Nutrition. doi: 10.1016/j.nut.2004.08.004 – volume: 29 start-page: 2359 year: 2010 ident: 1055_CR23 publication-title: Stat Med doi: 10.1002/sim.4006 – volume: 12 start-page: 1957 year: 2020 ident: 1055_CR40 publication-title: Nutrients. doi: 10.3390/nu12071957 – volume: 16 start-page: 78 year: 2015 ident: 1055_CR3 publication-title: J Zhejiang Univ Sci B. doi: 10.1631/jzus.B1400183 – volume: 32 start-page: 63 year: 2019 ident: 1055_CR33 publication-title: Biomed Environ Sci – volume: 31 start-page: e19 year: 2013 ident: 1055_CR5 publication-title: Cardiovasc Ther doi: 10.1111/1755-5922.12014 – volume: 38 start-page: 679 year: 2018 ident: 1055_CR26 publication-title: Arterioscler Thromb Vasc Biol doi: 10.1161/ATVBAHA.117.310211 – volume: 134 start-page: 288 year: 2014 ident: 1055_CR4 publication-title: Thromb Res doi: 10.1016/j.thromres.2014.05.025 – volume: 64 start-page: 1227 year: 2019 ident: 1055_CR15 publication-title: J Hum Genet doi: 10.1038/s10038-019-0672-7 – volume: 120 start-page: 1122 year: 2018 ident: 1055_CR10 publication-title: Br J Nutr doi: 10.1017/S0007114518002477 – volume: 119 start-page: 887 year: 2018 ident: 1055_CR17 publication-title: Br J Nutr doi: 10.1017/S0007114518000508 – volume: 23 start-page: 969 year: 2015 ident: 1055_CR37 publication-title: Eur J Hum Genet doi: 10.1038/ejhg.2014.212 – volume: 37 start-page: 319 year: 2019 ident: 1055_CR1 publication-title: J Bone Miner Metab doi: 10.1007/s00774-018-0920-5 – volume: 36 start-page: 528 year: 2017 ident: 1055_CR14 publication-title: J Am Coll Nutr doi: 10.1080/07315724.2017.1330162 – volume: 340 start-page: b4838 year: 2010 ident: 1055_CR22 publication-title: BMJ doi: 10.1136/bmj.b4838 – volume: 146 start-page: 627 year: 2020 ident: 1055_CR34 publication-title: Int J Cancer doi: 10.1002/ijc.32272 – volume: 74 start-page: 1677 year: 2020 ident: 1055_CR16 publication-title: Eur J Clin Nutr doi: 10.1038/s41430-020-0657-9 – volume: 141 start-page: 616 year: 2020 ident: 1055_CR21 publication-title: Circulation. doi: 10.1161/CIRCULATIONAHA.119.043805 – volume: 51 start-page: 1349 year: 2019 ident: 1055_CR35 publication-title: Nat Genet doi: 10.1038/s41588-019-0487-7 – volume: 17 start-page: 129. year: 2017 ident: 1055_CR39 publication-title: Curr Diabetes Rep doi: 10.1007/s11892-017-0961-5 – volume: 47 start-page: 456 year: 2000 ident: 1055_CR8 publication-title: Gut doi: 10.1136/gut.47.3.456 – volume: 36 start-page: 528 year: 2017 ident: 1055_CR11 publication-title: J Am Coll Nutr doi: 10.1080/07315724.2017.1330162 – volume: 95 start-page: e2652 year: 2016 ident: 1055_CR12 publication-title: Medicine doi: 10.1097/MD.0000000000002652 – volume: 22 start-page: 3777 year: 2016 ident: 1055_CR38 publication-title: World J Gastroenterol doi: 10.3748/wjg.v22.i14.3777 – volume: 135 start-page: 2091 year: 2017 ident: 1055_CR20 publication-title: Circulation. doi: 10.1161/CIRCULATIONAHA.116.024436 – volume: 70 start-page: 53 year: 2000 ident: 1055_CR27 publication-title: Mol Genet Metab doi: 10.1006/mgme.2000.2993 – volume: 11 start-page: Article 15 year: 2012 ident: 1055_CR24 publication-title: Stat Appl Genet Mol Biol doi: 10.1515/1544-6115.1796 – volume: 20 start-page: 2291 year: 2019 ident: 1055_CR19 publication-title: Brief Bioinform doi: 10.1093/bib/bby075 – volume: 17 start-page: 1157 year: 1997 ident: 1055_CR28 publication-title: Arterioscler Thromb Vasc Biol doi: 10.1161/01.ATV.17.6.1157 – volume: 37 start-page: 768 year: 2013 ident: 1055_CR31 publication-title: Genet Epidemiol doi: 10.1002/gepi.21762 – volume: 47 start-page: 1272 year: 2015 ident: 1055_CR36 publication-title: Nat Genet doi: 10.1038/ng.3368 – volume: 63 start-page: 18 year: 2009 ident: 1055_CR7 publication-title: Eur J Clin Nutr doi: 10.1038/sj.ejcn.1602897 – volume: 43 start-page: 1487 year: 2014 ident: 1055_CR9 publication-title: Int J Epidemiol doi: 10.1093/ije/dyu132 – volume: 527 start-page: 306 year: 2013 ident: 1055_CR2 publication-title: Gene. doi: 10.1016/j.gene.2013.06.041 |
SSID | ssj0014772 |
Score | 2.373593 |
Snippet | Background
Genetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed... Genetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed many single... BackgroundGenetic risk score (GRS) is a useful way to explore genetic architectures and the relationships of complex diseases. Several studies had revealed... |
SourceID | proquest pubmed crossref springer |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 943 |
SubjectTerms | 38 38/39 692/499 692/700/478/2772 Acids Betaine-homocysteine S-methyltransferase Clinical Nutrition Epidemiology Folic acid Hyperhomocysteinemia Internal Medicine Medicine Medicine & Public Health Metabolic Diseases Methylenetetrahydrofolate reductase Nucleotides Prediction models Public Health Risk analysis Risk factors Single-nucleotide polymorphism Vitamin B |
Title | Using the optimal method—explained variance weighted genetic risk score to predict the efficacy of folic acid therapy to hyperhomocysteinemia |
URI | https://link.springer.com/article/10.1038/s41430-021-01055-5 https://www.ncbi.nlm.nih.gov/pubmed/35001080 https://www.proquest.com/docview/2686426546 https://www.proquest.com/docview/2618501038 |
Volume | 76 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwEB5Be-GCoOURWiojIS5gNbt2EvuESmlVIbFCiEp7i_yKulI3WXZTyt74B1z4hfwSZpxkK1TBJQcncSLN2P7m9Q3ASxUMWg254q4KFcfdz3Dl5ZgLPApM5dORjT7dj5P87Fx-mGbT3uG26tMqhz0xbtS-ceQjPxznCqEyld68XXzl1DWKoqt9C427sE3UZaTVxXRjcI1kEZs3IYog739a9EUzqVCHK4lAIeWUoBB7RPLs74PpFtq8FSmNB9DpA7jfI0d21In6IdwJ9Q7sHtVoNc_X7BWLuZzRSb4DyftZaHGsZ_28ZJOBdH8XfsYsAYbAjzW4X8zxbtdG-vePX-H74tIg7vTsG9rQpBDsOvpOcQQ1jQoeGSWjsxWxX7K2YYslRXraOF0gOgrj1qypWEV8w8y4mWddideanr5Aq3d50cwbRwTS-KH5zDyC89OTL8dnvG_LwB1ivZY76RGVOOOddZnSZNMUqbeFDkSumHlrpRZa5aIw1nqhra6spLZVeSpkpivxGLbqpg5PgRXEjaj12OZay0Jphcapq0RaFfgWTpXA60Em5aJj3yhj1FyospNgiRIsowTLLIH9QWxlvxJX5Y3eJPBicxvXEAVGTB2aK3oGUQs1vFAJPOnEvfmcyMhsVmkCbwb530z-73959v9_2YN7Y6qjiHm_-7DVLq_Cc0Q3rT2IKoxXdTw6gO13J5NPn_8ALYn5kA |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3NbtQwEB6VcoALghZo2gJGAi5gNY3zYx8QqlqqLW331Eq9Bdtx1JW6ybKbUvbGG3DhOXgonoQZJ9kKVXDrNT9OpG9sf-OZ-QbglXQavYZUclu6kuPqp7ks4ogL3Ap0WYTbxp_pHg_TwWn86Sw5W4JffS0MpVX2a6JfqIva0hn5VpRKpMpUevNh8oVT1yiKrvYtNFqzOHTzK3TZZu8P9hDf11G0__Fkd8C7rgLcIlVpuI0L3FStLqyxiVREybOwMJlypA2YFMbESiiZikwbUwhlVGli6rqUhiJOVClw3DtwNxY4NakyfXeRUrIdZ75ZFLIWijaEWVekEwq5NYuRmIScEiJ8T0qe_L0R3mC3NyKzfsPbfwgPOqbKdlrTegRLrlqB1Z0KvfTxnL1hPnfUH8qvQLA3cg1e61RGL9iwF_lfhR8-K4Eh0WQ1rk9jvNu2rf79_af7NrnQyHML9hV9djJAduXPavEKWjYVWDJKfmczUttkTc0mU4osNX44R_IX2s5ZXbKS9I2ZtqOCtSVlc3r6HL3s6Xk9ri0JVuOHxiP9GE5vBbAnsFzVlVsDlpEWo1KRSZWKM6kkOsO2FGGZ4Vs4VABve0zySav2kfsovZB5i2COCOYewTwJYLOHLe9m_iy_ttMAXi5u45ylQIyuXH1JzyBLogYbMoCnLdyLz4mE3HQZBvCux_968H__y_r__-UF3BucHB_lRwfDww24H1ENh8853oTlZnrpniGzasxzb84MPt_2_PkDdDwztw |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3NbtQwEB6VIiEuCFqggQJGAi5gbRrnxz4gVHVZtRRWHKjUW4gdW12pmyy7KWVvvAEXnobH4UmYcZKtUAW3XvNjW5rx-BvPzDcAz6Qt0GtIJTfOOo7Wr-CyjCMu8CgoXBnuaH-n-2Gc7h_F746T4zX41dfCUFplbxO9oS5rQ3fkgyiVCJWp9GbgurSIj8PRm9kXTh2kKNLat9NoVeTQLs_RfVu8PhiirJ9H0ejtp7193nUY4AZhS8NNXOIBa4rSaJNIRfA8C0udKUs8gUmpdayEkqnICq1LobRyOqYOTGko4kQ5geNeg-uZyCTtMbm3Si_ZiTPfOAoRDEUewqwr2AmFHCxiBCkhp-QI35-SJ38fipeQ7qUorT_8RrfhVoda2W6rZndgzVYbsLlbocc-XbIXzOeR-gv6DQiGE9vgs45x9JSNe8L_TfjhMxQYgk5Wo62a4tu2hfXv7z_tt9lpgZi3ZF_RfydlZOf-3hafoJZTsSWjRHi2IOZN1tRsNqcoU-OHs0SFUZglqx1zxHXMCjMpWVtetqSvT9Djnp_U09oQeTVONJ0Ud-HoSgR2D9arurJbwDLiZVQq0qlScSaVRMfYOBG6DP_CoQJ42cskn7XMH7mP2AuZtxLMUYK5l2CeBLDdiy3vrMAiv9DZAJ6uXuP-paBMUdn6jL5BxETNNmQA91txr6YTCbnsMgzgVS__i8H_vZYH_1_LE7iBOyd_fzA-fAg3Iyrn8OnH27DezM_sIwRZjX7stZnB56vePn8AyoI37Q |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Using+the+optimal+method%E2%80%94explained+variance+weighted+genetic+risk+score+to+predict+the+efficacy+of+folic+acid+therapy+to+hyperhomocysteinemia&rft.jtitle=European+journal+of+clinical+nutrition&rft.au=Chen%2C+Xiaorui&rft.au=Huang%2C+Xiaowen&rft.au=Zheng%2C+Caifang&rft.au=Wang%2C+Xiliang&rft.date=2022-07-01&rft.pub=Nature+Publishing+Group+UK&rft.issn=0954-3007&rft.eissn=1476-5640&rft.volume=76&rft.issue=7&rft.spage=943&rft.epage=949&rft_id=info:doi/10.1038%2Fs41430-021-01055-5&rft.externalDocID=10_1038_s41430_021_01055_5 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0954-3007&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0954-3007&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0954-3007&client=summon |