Works matching IS 14712350 AND DT 2019 AND VI 20 AND IP 1

Results: 203

Genomic analysis of a spinal muscular atrophy (SMA) discordant family identifies a novel mutation in TLL2, an activator of growth differentiation factor 8 (myostatin): a case report.

Published in:

2019

By:

Jiang, Jianping;
Huang, Jinwei;
Gu, Jianlei;
Cai, Xiaoshu;
Zhao, Hongyu;
Lu, Hui

Publication type:

Case Study

A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0908-6

By:

Zaib, Tahir;
Ji, Wei;
Saleem, Komal;
Nie, Guangchen;
Li, Chao;
Cao, Lin;
Xu, Baijun;
Dong, Kexian;
Yu, Hanfei;
Hao, Xuguang;
Xue, Yan;
Si, Shuhan;
Jia, Xueyuan;
Wu, Jie;
Zhang, Xuelong;
Guan, Rongwei;
Ji, Guohua;
Bai, Jing;
Chen, Feng;
Liu, Yong

Publication type:

Article

POLE mutations improve the prognosis of endometrial cancer via regulating cellular metabolism through AMF/AMFR signal transduction.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0936-2

By:

Li, Yiran;
Bian, Yiding;
Wang, Kai;
Wan, Xiao-Ping

Publication type:

Article

Vitamin D receptor ApaI polymorphism associated with progression of liver disease in Vietnamese patients chronically infected with hepatitis B virus.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0903-y

By:

Hoan, Nghiem Xuan;
Khuyen, Nguyen;
Giang, Dao Phuong;
Binh, Mai Thanh;
Toan, Nguyen Linh;
Anh, Do Tuan;
Trung, Ngo Tat;
Bang, Mai Hong;
Meyer, Christian G.;
Velavan, Thirumalaisamy P.;
Song, Le Huu

Publication type:

Article

Identification of two novel COL10A1 heterozygous mutations in two Chinese pedigrees with Schmid-type metaphyseal chondrodysplasia.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0937-1

By:

Kong, Lingchi;
Shi, Li;
Wang, Wenbo;
Zuo, Rongtai;
Wang, Mengwei;
Kang, Qinglin

Publication type:

Article

Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0907-7

By:

Khan, Shazia;
Rawlins, Lettie E.;
Harlalka, Gaurav V.;
Umair, Muhammad;
Ullah, Asmat;
Shahzad, Shaheen;
Javed, Muhammad;
Baple, Emma L.;
Crosby, Andrew H.;
Ahmad, Wasim;
Gul, Asma

Publication type:

Article

Broadening the phenotype of the TWNK gene associated Perrault syndrome.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0934-4

By:

Fekete, Bálint;
Pentelényi, Klára;
Rudas, Gabor;
Gál, Anikó;
Grosz, Zoltán;
Illés, Anett;
Idris, Jimoh;
Csukly, Gabor;
Domonkos, Andor;
Molnar, Maria Judit

Publication type:

Article

Novel mutations identified in Chinese families with autosomal dominant congenital cataracts by targeted next-generation sequencing.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0933-5

By:

Li, Shan;
Zhang, Jianfei;
Cao, Yixuan;
You, Yi;
Zhao, Xiuli

Publication type:

Article

LRCH1 polymorphisms linked to delayed encephalopathy after acute carbon monoxide poisoning identified by GWAS analysis followed by Sequenom MassARRAY® validation.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0931-7

By:

Gu, Jiapeng;
Zeng, Jiao;
Wang, Xi;
Gu, Xin;
Zhang, Xiaoli;
Zhang, Ping;
Zhang, Fan;
Han, Yongkai;
Han, Yazhou;
Zhang, Hongxing;
Li, Wenqiang;
Gu, Renjun

Publication type:

Article

Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10.

Published in:

2019

By:

Khan, Amjad;
Wang, Rongrong;
Han, Shirui;
Umair, Muhammad;
Abbas, Safdar;
Khan, Muhammad Ismail;
Alshabeeb, Mohammad A.;
Alfadheland, Majid;
Zhang, Xue

Publication type:

Correction Notice

Association of vitamin D receptor TaqI and ApaI genetic polymorphisms with nephrolithiasis and end stage renal disease: a meta-analysis.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0932-6

By:

Hussain, Tajamul;
Naushad, Shaik M.;
Ahmed, Anwar;
Alamery, Salman;
Mohammed, Arif A.;
Abdelkader, Mohamed O.;
Alkhrm, Nasser Abobakr Nasser

Publication type:

Article

Novel gene mutation in von Hippel-Lindau disease – a report of two cases.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0930-8

By:

Wang, Jitian;
Cao, Wenjie;
Wang, Zhaoxia;
Zhu, Hong

Publication type:

Article

COL5A1 rs12722 polymorphism is not associated with passive muscle stiffness and sports-related muscle injury in Japanese athletes.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0928-2

By:

Miyamoto-Mikami, Eri;
Miyamoto, Naokazu;
Kumagai, Hiroshi;
Hirata, Kosuke;
Kikuchi, Naoki;
Zempo, Hirofumi;
Kimura, Noriko;
Kamiya, Nobuhiro;
Kanehisa, Hiroaki;
Naito, Hisashi;
Fuku, Noriyuki

Publication type:

Article

Identification of key pathways and genes in PTEN mutation prostate cancer by bioinformatics analysis.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0923-7

By:

Sun, Jian;
Li, Shugen;
Wang, Fei;
Fan, Caibin;
Wang, Jianqing

Publication type:

Article

Effects of factor v Leiden polymorphism on the pathogenesis and outcomes of preeclampsia.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0924-6

By:

Ababio, G. K.;
Adu-Bonsaffoh, K.;
Abindau, E.;
Narh, G.;
Tetteh, D.;
Botchway, F.;
Morvey, D.;
Neequaye, J.;
Quaye, I. K.

Publication type:

Article

A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-up.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0921-9

By:

Ryu, Jaehui;
Ko, Jung Min;
Shin, Choong-Ho

Publication type:

Article

Case report: two novel VPS13B mutations in a Chinese family with Cohen syndrome and hyperlinear palms.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0920-x

By:

Zhao, Sha;
Luo, Zhenqing;
Xiao, Zhenghui;
Li, Liping;
Zhao, Rui;
Yang, Yongjia;
Zhong, Yan

Publication type:

Article

Association between lncRNA H19 rs217727 polymorphism and the risk of cancer: an updated meta-analysis.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0904-x

By:

Wang, Xue;
Zhong, Jialing;
Chen, Fang;
Hu, Kang;
Sun, Suhong;
Leng, Yuanxiu;
Chen, Xumei;
Gan, Fengjiao;
Pan, Yana;
Luo, Qing

Publication type:

Article

SIRT1 (rs3740051) role in pituitary adenoma development.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0892-x

By:

Liutkeviciene, Rasa;
Vilkeviciute, Alvita;
Morkunaite, Greta;
Glebauskiene, Brigita;
Kriauciuniene, Loresa

Publication type:

Article

Prevalence of CCR5delta32 in Northeastern Iran.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0913-9

By:

Tajbakhsh, Amir;
Fazeli, Mostafa;
Rezaee, Mehdi;
Ghasemi, Faezeh;
Heravi, Mastoureh Momen;
Gholoobi, Aida;
Meshkat, Zahra

Publication type:

Article

Compound heterozygous LPIN2 pathogenic variants in a patient with Majeed syndrome with recurrent fever and severe neutropenia: case report.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0919-3

By:

Liu, Jun;
Hu, Xu-Yun;
Zhao, Zhi-Peng;
Guo, Ruo-Lan;
Guo, Jun;
Li, Wei;
Hao, Chan-Juan;
Xu, Bao-Ping

Publication type:

Article

Increased risk of aspirin-induced gastric mucosal erosion in elderly Chinese men harboring SLCO1B11b/1b while using aspirin and an ACEI or ARB concomitantly.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0918-4

By:

Duan, Lei;
Bai, Yongyi;
Li, Man;
Li, Huiying;
Li, Yanping;
Liu, Hongbin

Publication type:

Article

Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0912-x

By:

Zhang, Jingjing;
Ma, Dingyuan;
Liu, Gang;
Wang, Yuguo;
Liu, An;
Li, Li;
Luo, Chunyu;
Hu, Ping;
Xu, Zhengfeng

Publication type:

Article

Genetic polymorphisms associated with sleep-related phenotypes; relationships with individual nocturnal symptoms of insomnia in the HUNT study.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0916-6

By:

Bragantini, Daniela;
Sivertsen, Børge;
Gehrman, Philip;
Lydersen, Stian;
Güzey, Ismail Cüneyt

Publication type:

Article

Clinical and whole-exome sequencing findings in two siblings from Hani ethnic minority with congenital glycosylation disorders.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0902-z

By:

Zhang, Zhen;
Huang, Ti-Long;
Ma, Jing;
He, Wen-Ji;
Gu, Huaiyu

Publication type:

Article

Association of PD-1 polymorphisms with the risk and prognosis of lung adenocarcinoma in the northeastern Chinese Han population.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0914-8

By:

Huang, Kun;
Hu, Erqiang;
Li, Wan;
Lv, Junjie;
He, Yuehan;
Deng, Gui;
Xiao, Jinling;
Yang, Chengcheng;
Zhao, Xinyu;
Chen, Lina;
Wang, Xinyan

Publication type:

Article

Influence of oxytocin receptor single nucleotide sequence variants on contractility of human myometrium: an in vitro functional study.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0894-8

By:

Füeg, F.;
Santos, S.;
Haslinger, C.;
Stoiber, B.;
Schäffer, L.;
Grünblatt, E.;
Zimmermann, R.;
Simões-Wüst, A. P.

Publication type:

Article

Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0915-7

By:

Abou Hassan, Ossama K.;
Haidar, Wiam;
Arabi, Mariam;
Skouri, Hadi;
Bitar, Fadi;
Nemer, Georges;
Akl, Imad Bou

Publication type:

Article

Copy number variation is highly correlated with differential gene expression: a pan-cancer study.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0909-5

By:

Shao, Xin;
Lv, Ning;
Liao, Jie;
Long, Jinbo;
Xue, Rui;
Ai, Ni;
Xu, Donghang;
Fan, Xiaohui

Publication type:

Article

Cascade screening for familial hypercholesterolemia-identification of the C308Y mutation in multiple family members and relatives for the first time in mainland China.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0901-0

By:

Jin, Weirong;
Zhang, Qiuwang;
Wang, Bei;
Pan, Lili;
Qin, Hongyou;
Yang, Daying;
Zhou, Xiangqun;
Du, Yongcai;
Lin, Ling;
Kutryk, Michael J.

Publication type:

Article

A novel missense in GLI3 possibly affecting one of the zinc finger domains may lead to postaxial synpolydactyly: case report.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0889-5

By:

Zou, Qianqian;
Tian, Zhigang;
Zheng, Jie;
Zhi, Xiufang;
Du, Xiaojie;
Shu, Jianbo;
Cai, Chunquan

Publication type:

Article

Screening and computational analysis of colorectal associated non-synonymous polymorphism in CTNNB1 gene in Pakistani population.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0911-y

By:

Razak, Suhail;
Bibi, Nousheen;
Dar, Javid Ahmad;
Afsar, Tayyaba;
Almajwal, Ali;
Parveen, Zahida;
Jahan, Sarwat

Publication type:

Article

A case report and mechanism analysis of a normal phenotype mosaic 47, XXY complicated by paternal iUPD (9) who had a normal PGD result.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0897-5

By:

Li, Dan;
Wang, Yun;
Zhao, Nan;
Chang, Liang;
Liu, Ping;
Tian, Chan;
Qiao, Jie

Publication type:

Article

Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0917-5

By:

Ma, Cong;
Liu, Lv;
Wang, Fang-Na;
Tian, Hai-Shen;
Luo, Yan;
Yu, Rong;
Fan, Liang-Liang;
Li, Ya-Li

Publication type:

Article

Association of high sensitive C-reactive protein with coronary heart disease: a Mendelian randomization study.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0910-z

By:

Zhuang, Qian;
Shen, Chong;
Chen, Yanchun;
Zhao, Xianghai;
Wei, Pengfei;
Sun, Junxiang;
Ji, Yanni;
Chen, Xiaotian;
Yang, Song

Publication type:

Article

Associations of BAFF rs2893321 polymorphisms with myasthenia gravis susceptibility.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0906-8

By:

Deng, Hui;
Wang, Jianjian;
Kong, Xiaotong;
Zhang, Huixue;
Wang, Tianfeng;
Tian, Wenqi;
Yi, Tingting;
Wang, Lihua

Publication type:

Article

Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0895-7

By:

Khan, Amjad;
Wang, Rongrong;
Han, Shirui;
Umair, Muhammad;
Abbas, Safdar;
Khan, Muhammad Ismail;
Alshabeeb, Mohammad A.;
Alfadhel, Majid;
Zhang, Xue

Publication type:

Article

Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0893-9

By:

Mahjoub, Ghazale;
Habibzadeh, Parham;
Dastsooz, Hassan;
Mirzaei, Malihe;
Kavosi, Arghavan;
Jamali, Laila;
Javanmardi, Haniyeh;
Katibeh, Pegah;
Faghihi, Mohammad Ali;
Dastgheib, Seyed Alireza

Publication type:

Article

A steroid-resistant nephrotic syndrome in an infant resulting from a consanguineous marriage with COQ2 and ARSB gene mutations: a case report.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0898-4

By:

Wu, Xia;
Wang, Wenhong;
Liu, Yan;
Chen, Wenyu;
Zhao, Linsheng

Publication type:

Article

Decoding of novel missense TSC2 gene variants using in-silico methods.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0891-y

By:

Sudarshan, Shruthi;
Kumar, Manoj;
Kaur, Punit;
Kumar, Atin;
G., Sethuraman;
Sapra, Savita;
Gulati, Sheffali;
Gupta, Neerja;
Kabra, Madhulika;
Roy Chowdhury, Madhumita

Publication type:

Article

MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0905-9

By:

Khidri, Feriha Fatima;
Waryah, Yar Muhammad;
Ali, Faiza Kamran;
Shaikh, Hina;
Ujjan, Ikram Din;
Waryah, Ali Muhammad

Publication type:

Article

MMP-8 C-799 T, Lys460Thr, and Lys87Glu variants are not related to risk of cancer.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0890-z

By:

Zhang, Li-Feng;
Zhu, Li-Jie;
Zhang, Wei;
Yuan, Wei;
Song, Ning-Hong;
Zuo, Li;
Mi, Yuan-Yuan;
Wang, Zeng-Jun

Publication type:

Article

Pooling analysis regarding the impact of human vitamin D receptor variants on the odds of psoriasis.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0896-6

By:

Li, Juan;
Sun, Li;
Sun, Jinghui;
Yan, Min

Publication type:

Article

Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0899-3

By:

Olatunya, Oladele Simeon;
Albuquerque, Dulcineia Martins;
Akanbi, Ganiyu Olusola;
Aduayi, Olufunso Simisola;
Taiwo, Adekunle Bamidele;
Faboya, Opeyemi Ayodeji;
Kayode, Tolorunju Segun;
Leonardo, Daniela Pinheiro;
Adekile, Adekunle;
Costa, Fernando Ferreira

Publication type:

Article

IKZF1 genetic variants rs4132601 and rs11978267 and acute lymphoblastic leukemia risk in Tunisian children: a case-control study.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0900-1

By:

Mahjoub, Sana;
Chayeb, Vera;
Zitouni, Hedia;
Ghali, Rabeb M.;
Regaieg, Haifa;
Almawi, Wassim Y.;
Mahjoub, Touhami

Publication type:

Article

Clinical characteristics and mutation Spectrum of NF1 in 12 Chinese families with orbital/periorbital plexiform Neurofibromatosis type 1.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0877-9

By:

Chai, Peiwei;
Luo, Yingxiu;
Zhou, Chuandi;
Wang, Yefei;
Fan, Xianqun;
Jia, Renbing

Publication type:

Article

Metastatic colorectal cancer and severe hypocalcemia following irinotecan administration in a patient with X-linked agammaglobulinemia: a case report.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0880-1

By:

Li, Mingming;
Chen, Wei;
Sun, Xiaomeng;
Wang, Zhipeng;
Zou, Xun;
Wei, Hua;
Wang, Zhan;
Chen, Wansheng

Publication type:

Article

Genetic variants in CYP4F2 were significantly correlated with susceptibility to ischemic stroke.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0888-6

By:

Wu, Yuan;
Zhao, Junjie;
Zhao, Yonglin;
Huang, Tingqin;
Ma, Xudong;
Pang, Honggang;
Zhang, Ming

Publication type:

Article

Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0878-8

By:

Ngiwsara, Lukana;
Wattanasirichaigoon, Duangrurdee;
Tim-Aroon, Thipwimol;
Rojnueangnit, Kitiwan;
Noojaroen, Saisuda;
Khongkraparn, Arthaporn;
Sawangareetrakul, Phannee;
Ketudat-Cairns, James R.;
Charoenwattanasatien, Ratana;
Champattanachai, Voraratt;
Kuptanon, Chulaluck;
Pangkanon, Suthipong;
Svasti, Jisnuson

Publication type:

Article

Screening of 31 genes involved in monogenic forms of obesity in 23 Pakistani probands with early-onset childhood obesity: a case report.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0886-8

By:

Niazi, Robina Khan;
Gjesing, Anette Prior;
Hollensted, Mette;
Have, Christian Theil;
Borisevich, Dmitrii;
Grarup, Niels;
Pedersen, Oluf;
Ullah, Asmat;
Shahid, Gulbin;
Shafqat, Ifrah;
Gul, Asma;
Hansen, Torben

Publication type:

Article