Works matching IS 14739542 AND DT 2019 AND VI 13 AND IP 1

Results: 58

Associations between microRNA (miR-25, miR-32, miR-125, and miR-222) polymorphisms and recurrent implantation failure in Korean women.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0246-y

By:

Lee, Jeong Yong;
Ahn, Eun Hee;
Kim, Jung Oh;
Park, Han Sung;
Ryu, Chang Soo;
Kim, Ji Hyang;
Kim, Young Ran;
Lee, Woo Sik;
Kim, Nam Keun

Publication type:

Article

Downregulation of miR-542-3p promotes osteogenic transition of vascular smooth muscle cells in the aging rat by targeting BMP7.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0245-z

By:

Liu, Huan;
Wang, Hongwei;
Yang, Sijin;
Qian, Dehui

Publication type:

Article

The multi-faceted functioning portrait of LRF/ZBTB7A.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0252-0

By:

Constantinou, Caterina;
Spella, Magda;
Chondrou, Vasiliki;
Patrinos, George P.;
Papachatzopoulou, Adamantia;
Sgourou, Argyro

Publication type:

Article

Investigating RNA expression profiles altered by nicotinamide mononucleotide therapy in a chronic model of alcoholic liver disease.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0251-1

By:

Assiri, Mohammed A.;
Ali, Hadi R.;
Marentette, John O.;
Yun, Youngho;
Liu, Juan;
Hirschey, Matthew D.;
Saba, Laura M.;
Harris, Peter S.;
Fritz, Kristofer S.

Publication type:

Article

Human genetics and genomics research in Ecuador: historical survey, current state, and future directions.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0249-8

By:

Zambrano-Mila, Marlon S.;
Agathos, Spiros N.;
Reichardt, Juergen K. V.

Publication type:

Article

Association between polymorphism in CDKN2B-AS1 gene and its interaction with smoking on the risk of lung cancer in a Chinese population.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0240-4

By:

Lv, Xiaoting;
Cui, Zhigang;
Li, Hang;
Li, Juan;
Yang, Zitai;
Bi, Yanhong;
Gao, Min;
Zhang, Ziwei;
Wang, Shengli;
Zhou, Baosen;
Yin, Zhihua

Publication type:

Article

Common polymorphic inversions at 17q21.31 and 8p23.1 associate with cancer prognosis.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0242-2

By:

Ruiz-Arenas, Carlos;
Cáceres, Alejandro;
Moreno, Victor;
González, Juan R.

Publication type:

Article

Genetics and functions of the retinoic acid pathway, with special emphasis on the eye.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0248-9

By:

Thompson, Brian;
Katsanis, Nicholas;
Apostolopoulos, Nicholas;
Thompson, David C.;
Nebert, Daniel W.;
Vasiliou, Vasilis

Publication type:

Article

Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical features.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0250-2

By:

Chen, Yibo;
Yu, Qi;
Mao, Xiongying;
Lei, Wei;
He, Miaonan;
Lu, Wenbo

Publication type:

Article

Transcriptomic analysis of monocytes from HIV-positive men on antiretroviral therapy reveals effects of tobacco smoking on interferon and stress response systems associated with depressive symptoms.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0247-x

By:

Lorenz, David R.;
Misra, Vikas;
Gabuzda, Dana

Publication type:

Article

EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0238-y

By:

Wu, Jing;
Yang, Yi;
He, You;
Li, Qiang;
Wang, Xu;
Sun, Chengjun;
Wang, Lishun;
An, Yu;
Luo, Feihong

Publication type:

Article

Factors affecting cell-free DNA fetal fraction: statistical analysis of 13,661 maternal plasmas for non-invasive prenatal screening.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0244-0

By:

Hou, Yaping;
Yang, Jiexia;
Qi, Yiming;
Guo, Fangfang;
Peng, Haishan;
Wang, Dongmei;
Wang, Yixia;
Luo, Xiaohui;
Li, Yi;
Yin, Aihua

Publication type:

Article

Genetic variants of VEGFR-1 gene promoter in acute myocardial infarction.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0243-1

By:

Wang, Haihua;
Zhang, Shufang;
Wang, Na;
Zhang, Jie;
Chen, Mingkai;
He, Xiaohui;
Cui, Yinghua;
Pang, Shuchao;
Yan, Bo

Publication type:

Article

Copy number of 8q24.3 drives HSF1 expression and patient outcome in cancer: an individual patient data meta-analysis.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0241-3

By:

Brusselaers, Nele;
Ekwall, Karl;
Durand-Dubief, Mickael

Publication type:

Article

Identification of key candidate genes and molecular pathways in white fat browning: an anti-obesity drug discovery based on computational biology.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0239-x

By:

Pan, Yuyan;
Liu, Jiaqi;
Qi, Fazhi

Publication type:

Article

lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cells.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0237-z

By:

Li, Qian;
Zhang, Jing;
Su, Dong-Mei;
Guan, Li-Na;
Mu, Wei-Hong;
Yu, Mei;
Ma, Xu;
Yang, Rong-Juan

Publication type:

Article

Novel analytical methods to interpret large sequencing data from small sample sizes.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0235-1

By:

Lichou, Florence;
Orazio, Sébastien;
Dulucq, Stéphanie;
Etienne, Gabriel;
Longy, Michel;
Hubert, Christophe;
Groppi, Alexis;
Monnereau, Alain;
Mahon, François-Xavier;
Turcq, Béatrice

Publication type:

Article

Three miRNAs cooperate with host genes involved in human cardiovascular disease.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0232-4

By:

Zhu, Yan;
Xie, Jingjing;
Sun, Hong

Publication type:

Article

Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0229-z

By:

Krebs, Kristi;
Milani, Lili

Publication type:

Article

Diversity of ATM gene variants: a population-based genome data analysis for precision medicine.

Published in:

2019

By:

Fukunaga, Hisanori;
Taki, Yasuyuki;
Prise, Kevin M.

Publication type:

Letter

Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0231-5

By:

Went, Molly;
Kinnersley, Ben;
Sud, Amit;
Johnson, David C.;
Weinhold, Niels;
Försti, Asta;
van Duin, Mark;
Orlando, Giulia;
Mitchell, Jonathan S.;
Kuiper, Rowan;
Walker, Brian A.;
Gregory, Walter M.;
Hoffmann, Per;
Jackson, Graham H.;
Nöthen, Markus M.;
da Silva Filho, Miguel Inacio;
Thomsen, Hauke;
Broyl, Annemiek;
Davies, Faith E.;
Thorsteinsdottir, Unnur

Publication type:

Article

Identification and potential mechanisms of a 4-lncRNA signature that predicts prognosis in patients with laryngeal cancer.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0230-6

By:

Zhang, Guihai;
Fan, Erxi;
Zhong, Qiuyue;
Feng, Guangyong;
Shuai, Yu;
Wu, Mingna;
Chen, Qiying;
Gou, Xiaoxia

Publication type:

Article

Next-generation sequencing in liquid biopsy: cancer screening and early detection.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0220-8

By:

Chen, Ming;
Zhao, Hongyu

Publication type:

Article

Meeting report: the Human Genome Meeting (HGM) 2019 in Seoul, Korea.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0218-2

By:

Solano, Angela;
Novelli, Giuseppe;
Baghat, Shruti;
Carnici, Piero;
van Ommen, Gert-Jan;
Reichardt, Juergen K. V.

Publication type:

Article

Identification of a novel long non-coding RNA within RUNX1 intron 5.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0219-1

By:

Schnake, Nicolás;
Hinojosa, Marcela;
Gutiérrez, Soraya

Publication type:

Article

Helicobacter pylori infection, serum pepsinogens as markers of atrophic gastritis, and leukocyte telomere length: a population-based study.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0217-3

By:

Muhsen, Khitam;
Sinnreich, Ronit;
Merom, Dafna;
Nassar, Hisham;
Cohen, Dani;
Kark, Jeremy D.

Publication type:

Article

Essential genetic findings in neurodevelopmental disorders.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0216-4

By:

Cardoso, Ana R.;
Lopes-Marques, Mónica;
Silva, Raquel M.;
Serrano, Catarina;
Amorim, António;
Prata, Maria J.;
Azevedo, Luísa

Publication type:

Article

A novel knowledge-derived data potentizing method revealed unique liver cancer-associated genetic variants.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0213-7

By:

Sultana, Naznin;
Rahman, Mijanur;
Myti, Sanat;
Islam, Jikrul;
Mustafa, Md. G.;
Nag, Kakon

Publication type:

Article

Correction to: Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.

Published in:

2019

By:

Voskarides, Konstantinos;
Dweep, Harsh;
Chrysostomou, Charalambos

Publication type:

Correction Notice

Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0212-8

By:

Lee, Eunkyung;
Takita, Cristiane;
Wright, Jean L.;
Slifer, Susan H.;
Martin, Eden R.;
Urbanic, James J.;
Langefeld, Carl D.;
Lesser, Glenn J.;
Shaw, Edward G.;
Hu, Jennifer J.

Publication type:

Article

Interplay Between the Host, the Human Microbiome, and Drug Metabolism.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0211-9

By:

Nichols, Robert G.;
Peters, Jeffrey M.;
Patterson, Andrew D.

Publication type:

Article

Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.

Published in:

2019

By:

Voskarides, Konstantinos;
Dweep, Harsh;
Chrysostomou, Charalambos

Publication type:

Letter

Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.

Published in:

2019

By:

Voskarides, Konstantinos;
Dweep, Harsh;
Chrysostomou, Charalambos

Publication type:

Letter

IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0209-3

By:

Zhytnik, Lidiia;
Maasalu, Katre;
Duy, Binh Ho;
Pashenko, Andrey;
Khmyzov, Sergey;
Reimann, Ene;
Prans, Ele;
Kõks, Sulev;
Märtson, Aare

Publication type:

Article

Statement on bioinformatics and capturing the benefits of genome sequencing for society.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0208-4

By:

Capps, Benjamin;
Chadwick, Ruth;
Joly, Yann;
Lysaght, Tamra;
Mills, Catherine;
Mulvihill, John J.;
Zwart, Hub

Publication type:

Article

What influences public views on forensic DNA testing in the criminal field? A scoping review of quantitative evidence.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0207-5

By:

Machado, Helena;
Silva, Susana

Publication type:

Article

Genetics of heart rate in heart failure patients (GenHRate).

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0206-6

By:

Evans, Kaleigh L.;
Wirtz, Heidi S.;
Li, Jia;
She, Ruicong;
Maya, Juan;
Gui, Hongsheng;
Hamer, Andrew;
Depre, Christophe;
Lanfear, David E.

Publication type:

Article

Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0205-7

By:

Guan, Meijian;
Keaton, Jacob M.;
Dimitrov, Latchezar;
Hicks, Pamela J.;
Xu, Jianzhao;
Palmer, Nicholette D.;
Ma, Lijun;
Das, Swapan K.;
Chen, Yii-Der I.;
Coresh, Josef;
Fornage, Myriam;
Franceschini, Nora;
Kramer, Holly;
Langefeld, Carl D.;
Mychaleckyj, Josyf C.;
Parekh, Rulan S.;
Post, Wendy S.;
Rasmussen-Torvik, Laura J.;
Rich, Stephen S.;
Rotter, Jerome I.

Publication type:

Article

Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0204-8

By:

Cavalli, Marco;
Baltzer, Nicholas;
Pan, Gang;
Bárcenas Walls, José Ramón;
Smolinska Garbulowska, Karolina;
Kumar, Chanchal;
Skrtic, Stanko;
Komorowski, Jan;
Wadelius, Claes

Publication type:

Article

Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0203-9

By:

Spataro, Rossella;
Kousi, Maria;
Farhan, Sali M. K.;
Willer, Jason R.;
Ross, Jay P.;
Dion, Patrick A.;
Rouleau, Guy A.;
Daly, Mark J.;
Neale, Benjamin M.;
La Bella, Vincenzo;
Katsanis, Nicholas

Publication type:

Article

The significance of trisomy 7 mosaicism in noninvasive prenatal screening.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0201-y

By:

Qi, Yiming;
Yang, Jiexia;
Hou, Yaping;
Guo, Fangfang;
Peng, Haishan;
Wang, Dongmei;
Du, Qianyi;
Yin, Aihua

Publication type:

Article

Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0202-x

By:

Tekola-Ayele, Fasil;
Lee, Anthony;
Workalemahu, Tsegaselassie;
Sánchez-Pozos, Katy

Publication type:

Article

Correction to: The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau.

Published in:

2019

By:

Charati, Hadi;
Peng, Min-Sheng;
Chen, Wei;
Yang, Xing-Yan;
Ori, Roghayeh Jabbari;
Aghajanpour-Mir, Mohsen;
Esmailizadeh, Ali;
Zhang, Ya-Ping

Publication type:

Correction Notice

Transcriptome-wide analysis of differentially expressed chemokine receptors, SNPs, and SSRs in the age-related macular degeneration.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0199-1

By:

Saddala, Madhu Sudhana;
Lennikov, Anton;
Mukwaya, Anthony;
Fan, Lijuan;
Hu, Zhengmao;
Huang, Hu

Publication type:

Article

Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0198-2

By:

Hu, Hua;
Wang, Li;
Wu, Jiayan;
Zhou, Peng;
Fu, Jingli;
Sun, Jiuchen;
Cai, Weiyi;
Liu, Hailiang;
Yang, Ying

Publication type:

Article

Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0197-3

By:

Mohamad, Nur Afiqah;
Ramachandran, Vasudevan;
Mohd Isa, Hazlita;
Chan, Yoke Mun;
Ngah, Nor Fariza;
Ching, Siew Mooi;
Hoo, Fan Kee;
Wan Sulaiman, Wan Aliaa;
Inche Mat, Liyana Najwa;
Mohamed, Mohd Hazmi

Publication type:

Article

Association of genetic ancestry with colorectal tumor location in Puerto Rican Latinos.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0196-4

By:

Pérez-Mayoral, Julyann;
Soto-Salgado, Marievelisse;
Shah, Ebony;
Kittles, Rick;
Stern, Mariana C.;
Olivera, Myrta I.;
Gonzalez-Pons, María;
Rodriguez-Quilichinni, Segundo;
Torres, Marla;
Reyes, Jose S.;
Tous, Luis;
López, Nicolas;
Chevere, Victor Carlo;
Cruz-Correa, Marcia

Publication type:

Article

Update on the human and mouse lipocalin (LCN) gene family, including evidence the mouse Mup cluster is result of an "evolutionary bloom".

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0191-9

By:

Charkoftaki, Georgia;
Wang, Yewei;
McAndrews, Monica;
Bruford, Elspeth A.;
Thompson, David C.;
Vasiliou, Vasilis;
Nebert, Daniel W.

Publication type:

Article

Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0192-8

By:

Lam, Phuong T.;
Padula, Stephanie L.;
Hoang, Thanh V.;
Poth, Justin E.;
Liu, Lin;
Liang, Chun;
LeFever, Adam S.;
Wallace, Lindsay M.;
Ashery-Padan, Ruth;
Riggs, Penny K.;
Shields, Jordan E.;
Shaham, Ohad;
Rowan, Sheldon;
Brown, Nadean L.;
Glaser, Tom;
Robinson, Michael L.

Publication type:

Article

vi-HMM: a novel HMM-based method for " sequence variant identification in short-read data.

Published in:

Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0194-6

By:

Man Tang;
Hasan, Mohammad Shabbir;
Hongxiao Zhu;
Liqing Zhang;
Xiaowei Wu

Publication type:

Article