Ecosyste.ms: Papers
An open API service providing mapping between scientific papers and software projects that are mentioned in them.
All mentions data is based on the CZI Software Mentions dataset.
Projects: pypi: 2
https://packages.ecosyste.ms/registries/pypi.org/packages/2
Papers Mentioning 2 499
10.1186/s12966-014-0154-4
Gender differences on effectiveness of a school-based physical activity intervention for reducing cardiometabolic risk: a cluster randomized trialCited by: 44
Author(s): Vicente Martínez‐Vizcaíno, Mairena Sánchez‐López, Blanca Notario‐Pacheco, Fernando Salcedo-Aguilar, Montserrat Solera-Martínez, Pablo Franquelo-Morales, Sara López-Martínez, Jorge Cañete García-Prieto, Natalia María Arias-Palencia, Coral Torrijos-Niño, Ricardo Mora-Rodríguez, Fernando Rodríguez‐Artalejo
Software Mentions: 1
Published: about 10 years ago
10.1002/2015JF003504
Rapid advance of two mountain glaciers in response to mine-related debris loadingCited by: 17
Author(s): Stewart S. R. Jamieson, Marek Ewertowski, David J. A. Evans
Software Mentions: 1
Published: over 9 years ago
10.7189/jogh.10.010425
Impact of mobile health-enhanced supportive supervision and supply chain management on appropriate integrated community case management of malaria, diarrhoea, and pneumonia in children 2-59 months: A cluster randomised trial in Eastern Province, ZambiaCited by: 10
Author(s): Godfrey Biemba, Boniface Chiluba, Kojo Yeboah-Antwi, Vichael Silavwe, Karsten Lunze, Rodgers Mwale, Davidson H. Hamer, W. Bentley MacLeod
Software Mentions: 1
Published: over 4 years ago
10.1155/2020/3129356
The Novel Role of Healing from Bacterial Infections of Lower Limb Open Fractures by X-Ray ExposureCited by: 2
Author(s): Ali Abdul Hussein Mahdi, Tuqa S. Al-Salmani, Mustafa M. Al-Qaisi
Software Mentions: 1
Published: over 4 years ago
10.3892/ijmm.2014.1929
Inspissated bile syndrome in an infant with citrin deficiency and congenital anomalies of the biliary tract and esophagus: Identification and pathogenicity analysis of a novel SLC25A13 mutation with incomplete penetranceCited by: 12
Author(s): Han‐Shi Zeng, Shutao Zhao, Mei Deng, Zhan‐Hui Zhang, Xiang‐Ran Cai, Fengping Chen, Yuan‐Zong Song
Software Mentions: 1
Published: about 10 years ago
10.1002/jmd2.12027
A novel mutation in <i>VPS33B</i> gene causing a milder ARC syndrome phenotype with prolonged survivalCited by: 11
Author(s): R Castillo, James E. Squires, Patrick McKiernan
Software Mentions: 1
Published: over 5 years ago
10.1002/jmd2.12058
Iron‐sulfur cluster ISD11 deficiency ( <i>LYRM4</i> gene) presenting as cardiorespiratory arrest and 3‐methylglutaconic aciduriaCited by: 7
Author(s): Margarida Paiva Coelho, Joana Correia, Aureliano Dias, Célia Nogueira, Anabela Bandeira, Esmeralda Martins, Laura Vilarinho
Software Mentions: 1
Published: over 5 years ago
10.1002/jmd2.12197
Familial variability of cerebrotendinous xanthomatosis lacking typical biochemical findingsCited by: 6
Author(s): Adam J. Guenzel, Andrea E. DeBarber, Kimiyo Raymond, Radhika Dhamija
Software Mentions: 1
Published: almost 4 years ago
10.1002/jmd2.12214
Functional assessment of the genetic findings indicating mucopolysaccharidosis type <scp>II</scp> in the prenatal settingCited by: 1
Author(s): Maria Fuller, David Ketteridge
Software Mentions: 1
Published: over 3 years ago
10.1111/1756-185X.13921
Diagnostic accuracy of 14‐3‐3 η protein in rheumatoid arthritis: A meta‐analysisCited by: 6
Author(s): Decai Wang, Yalan Cui, Huiren Lei, Ding Cao, Guoting Tang, Haiming Huang, Ting Yuan, Lizong Rao, Biwen Mo
Software Mentions: 1
Published: about 4 years ago
10.29252/ibj.23.6.412
Association of a New Germline Variant in the MUTYH DNA Glycosylase Gene with Colorectal Adenoma Transformation into MalignancyCited by: 0
Author(s): Amjad Mahasneh, Fawaz N. Al-Shaheri, Mohammed N. Banihani
Software Mentions: 1
Published: about 5 years ago
10.3390/ijerph17249289
Multi-Objective Optimal Allocation of Water Resources Based on the NSGA-2 Algorithm While Considering Intergenerational Equity: A Case Study of the Middle and Upper Reaches of Huaihe River Basin, ChinaCited by: 13
Author(s): Jitao Zhang, Zengchuan Dong, Chuanmao Tian
Software Mentions: 1
Published: almost 4 years ago
10.3390/ijerph18052365
Effectiveness of Conservative Treatment According to Severity and Systemic Disease in Carpal Tunnel Syndrome: A Systematic ReviewCited by: 17
Author(s): Mar Hernández-Secorún, Raquel Montaña-Cortés, César Hidalgo-García, Jacobo Rodríguez-Sanz, Jaime Corral-de-Toro, Sofía Monti-Ballano, Sami Hamam-Alcober, José Miguel Tricás-Moreno, María Orosia Lucha-López
Software Mentions: 1
Published: almost 4 years ago
10.3390/ijerph18168500
Impact of Sexual Activity on the Risk of Male Genital Tumors: A Systematic Review of the LiteratureCited by: 28
Author(s): Felice Crocetto, Davide Arcaniolo, Luigi Napolitano, Biagio Barone, Roberto La Rocca, Marco Capece, Vincenzo Caputo, Ciro Imbimbo, Marco De Sio, Francesco Paolo Calace, Celeste Manfredi
Software Mentions: 1
Published: over 3 years ago
10.2196/13384
Accuracy of Fitbit Wristbands in Measuring Sleep Stage Transitions and the Effect of User-Specific FactorsCited by: 50
Author(s): Zilu Liang, Mario Alberto Chapa Martell
Software Mentions: 1
Published: over 5 years ago
10.2196/10733
Clinical Applications of Mobile Health Wearable–Based Sleep Monitoring: Systematic ReviewCited by: 68
Author(s): Élise Guillodo, Christophe Lemey, Mathieu Simonnet, Michel Walter, Enrique Baca‐García, Vincent Masetti, Sorin Moga, Mark E. Larsen, Juliette Ropars, Sofian Berrouiguet
Software Mentions: 1
Published: over 4 years ago
10.1007/s10545-014-9747-y
Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotypeCited by: 29
Author(s): Ann Bowron, J. Honeychurch, Maggie Williams, Beverly Tsai-Goodman, Nicol Clayton, Lucy Jones, Graham Shortland, Shakeel Qureshi, Simon Heales, Colin G. Steward
Software Mentions: 1
Published: over 10 years ago
10.1002/jmri.26649
Fast myocardial T<sub>1</sub> mapping using shortened inversion recovery based schemesCited by: 7
Author(s): Li Huang, Radhouène Neji, Muhummad Sohaib Nazir, John Whitaker, Fiona Reid, Filippo Bosio, Amedeo Chiribiri, Reza Razavi, Sébastien Roujol
Software Mentions: 1
Published: almost 6 years ago
10.1136/jmedgenet-2020-107048
Biallelic variants in <i>ADARB1</i>, encoding a dsRNA-specific adenosine deaminase, cause a severe developmental and epileptic encephalopathyCited by: 12
Author(s): Reza Maroofian, Jiří Sedmík, Neda Mazaheri, Marcello Scala, Maha S. Zaki, Liam P. Keegan, Reza Azizimalamiri, Mahmoud Y. Issa, Gholamreza Shariati, Alireza Sedaghat, Christian Beetz, Péter Bauer, Hamid Galehdari, Mary A. O’Connell, Henry Houlden
Software Mentions: 1
Published: over 4 years ago
10.7554/eLife.52483
Dissecting transcriptional amplification by MYCCited by: 37
Author(s): Zhongzhen Nie, Chunhua Guo, Subhendu Das, C. C. Chow, Eric Batchelor, S. Stoney Simons, David Levens
Software Mentions: 1
Published: over 4 years ago
10.3390/ijms20040937
Gene-Specific Intron Retention Serves as Molecular Signature that Distinguishes Melanoma from Non-Melanoma Cancer Cells in Greek PatientsCited by: 7
Author(s): Aikaterini F. Giannopoulou, Eumorphia G. Konstantakou, Athanassios D. Velentzas, Socratis Avgeris, Margaritis Avgeris, Νικολαοσ Παπανδρεου, Ilianna Zoi, Vicky Filippa, Stamatia A. Katarachia, Antonis D. Lampidonis, Anastasia Prombona, Popi Syntichaki, Christina Piperi, Efthimia K. Basdra, Vassiliki A. Iconomidou, Evangelia Papadavid, Ema Anastasiadou, Issidora S. Papassideri, Athanasios G. Papavassiliou, Gerassimos E. Voutsinas, Andreas Scorilas, Dimitrios J. Stravopodis
Software Mentions: 1
Published: almost 6 years ago
10.3390/ijms20215351
Structural Insights into AQP2 Targeting to Multivesicular BodiesCited by: 10
Author(s): J Roche, Veronika Nešverová, Catharina Olsson, Peter M.T. Deen, Susanna Törnroth-Horsefield
Software Mentions: 1
Published: about 5 years ago
10.3390/ijms20225619
Transcription Factor Prospero Homeobox 1 (PROX1) as a Potential Angiogenic Regulator of Follicular Thyroid Cancer DisseminationCited by: 14
Author(s): Magdalena Rudzińska, Michał Mikula, Katarzyna D. Arczewska, Ewa Gajda, Stanisława Sabalińska, Tomasz Stępień, Jerzy Ostrowski, Barbara Czarnocka
Software Mentions: 1
Published: about 5 years ago
10.3390/ijms21114160
Novel Polymorphisms and Genetic Characteristics of the Prion Protein Gene (PRNP) in Dogs—A Resistant Animal of Prion DiseaseCited by: 14
Author(s): Dong-Ju Kim, Yongchan Kim, An-Dang Kim, Byung‐Hoon Jeong
Software Mentions: 1
Published: over 4 years ago
10.3390/ijms21124246
First Report of the Potential Bovine Spongiform Encephalopathy (BSE)-Related Somatic Mutation E211K of the Prion Protein Gene (PRNP) in CattleCited by: 14
Author(s): Sae-Young Won, Yongchan Kim, Byung‐Hoon Jeong
Software Mentions: 1
Published: over 4 years ago
10.3390/ijms21186641
Molecular Modeling of Pathogenic Mutations in the Keratin 1B DomainCited by: 5
Author(s): Alexander J Hinbest, Sherif A. Eldirany, Minh Ho, Christopher G. Bunick
Software Mentions: 1
Published: about 4 years ago
10.3390/ijms22158048
Computational Insights into the Deleterious Impacts of Missense Variants on N-Acetyl-d-glucosamine Kinase Structure and FunctionCited by: 6
Author(s): Raju Dash, Sarmistha Mitra, Yeasmin Akter Munni, Hyung Jun Choi, Md. Chayan Ali, Largess Barua, Tae Jung Jang, Il Soo Moon
Software Mentions: 1
Published: over 3 years ago
10.2196/18580
An Electronic Data Capture Framework (ConnEDCt) for Global and Public Health Research: Design and ImplementationCited by: 17
Author(s): Caleb Ruth, Samantha L Huey, Jesse T Krisher, Amy Fothergill, Bryan M Gannon, Camille Jones, Elizabeth Centeno‐Tablante, Laura Hackl, Susannah Colt, Julia L. Finkelstein, Saurabh Mehta
Software Mentions: 1
Published: over 4 years ago
10.1186/1742-2094-10-86
Diverse activation of microglia by chemokine (C-C motif) ligand 2 overexpression in brainCited by: 73
Author(s): Maj Linda B. Selenica, Jennifer Alvarez, Kevin Nash, Daniel Lee, Chuanhai Cao, Xiaoyang Lin, Patrick Reid, Peter R. Mouton, Dave Morgan, Marcia N. Gordon
Software Mentions: 1
Published: over 11 years ago
10.1136/jnnp-2014-309845
Performance characteristics of methods for quantifying spontaneous intracerebral haemorrhage: data from the Efficacy of Nitric Oxide in Stroke (ENOS) trialCited by: 30
Author(s): Kailash Krishnan, S. F. Mukhtar, James Lingard, Aimee Houlton, Elizabeth Walker, Tanya Jones, Nikola Sprigg, L.A. Cala, Jennifer Becker, Robert A. Dineen, Panos Koumellis, Alessandro Adami, Ana M. Casado, Philip M Bath, Joanna M. Wardlaw
Software Mentions: 1
Published: almost 10 years ago
10.1155/2021/8883946
Accuracy of Deep Learning Algorithms for the Diagnosis of Retinopathy of Prematurity by Fundus Images: A Systematic Review and Meta-AnalysisCited by: 10
Author(s): Jingjing Zhang, Yangyang Liu, Toshiharu Mitsuhashi, Toshihiko Matsuo
Software Mentions: 1
Published: over 3 years ago
10.18632/oncotarget.16614
Association of CKIP-1 P21A polymorphism with risk of chronic heart failure in a Chinese populationCited by: 6
Author(s): Mu-Peng Li, Yan-Jiao Zhang, Xiaolei Hu, Jiahao Zhou, Yang Yi, Lihua Peng, Hong Qiang, Tianlun Yang, Xiaoping Chen
Software Mentions: 1
Published: over 7 years ago
10.18632/oncotarget.21739
Systematic review and critique of circulating miRNAs as biomarkers of stage I-II non-small cell lung cancerCited by: 44
Author(s): Francesca Moretti, Paola D’Antona, Emanuele Finardi, Marco Barbetta, Lorenzo Dominioni, Albino Poli, Elisabetta Gini, Daniel J. Noonan, Andrea Imperatori, Nicola Rotolo, Maria Cattoni, Paola Campomenosi
Software Mentions: 1
Published: about 7 years ago
10.18632/oncotarget.19024
The performance of 11C-Methionine PET in the differential diagnosis of glioma recurrenceCited by: 39
Author(s): Weilin Xu, Liansheng Gao, Anwen Shao, Jingwei Zheng, Jianmin Zhang
Software Mentions: 1
Published: over 7 years ago
10.18632/oncotarget.22116
Development and validation of a targeted next generation DNA sequencing panel outperforming whole exome sequencing for the identification of clinically relevant genetic variantsCited by: 20
Author(s): Eirwen M. Miller, Nicole E. Patterson, Jenna Marcus Zechmeister, Michal Bejerano‐Sagie, Maria Delio, Kavisha Patel, Nivedita Ravi, Wilber Quispe-Tintaya, Alexander Y. Maslov, Nichelle Simmons, Maria Castaldi, Jan Vijg, Rouzan G. Karabakhtsian, John M. Greally, D.Y.S. Kuo, Cristina Montagna
Software Mentions: 1
Published: about 7 years ago
10.18632/oncotarget.22359
miR-1271 inhibits ERα expression and confers letrozole resistance in breast cancerCited by: 10
Author(s): Tao Yu, Hairu Yu, Jiayi Sun, Zhao Zhao, Shuang Li, Xinfeng Zhang, Zhi-Xuan Liao, Mingke Cui, Juan Li, Chan Li, Qiang Zhang
Software Mentions: 1
Published: about 7 years ago
10.18632/oncotarget.10525
Genetic and functional analysis of two missense <i>DUOX2</i> mutations in congenital hypothyroidism and goiterCited by: 12
Author(s): Shiguo Liu, Wenhui Zhang, Liqin Zhang, Hui Zou, Kunna Lu, Qiang Li, Hong-Fei Xia, Shushan Yan, Xu Ma
Software Mentions: 1
Published: over 8 years ago
10.18632/oncotarget.26674
The value of arterial spin labelling in adults glioma grading: systematic review and meta-analysisCited by: 21
Author(s): Amirah Alsaedi, Fabio Martino Doniselli, Hans Rolf Jäger, Jasmina Panovska‐Griffiths, Antonio Rojas-García, Xavier Golay, Sotirios Bisdas
Software Mentions: 1
Published: almost 6 years ago
10.1186/s13023-021-01995-y
Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East AsiaCited by: 2
Author(s): Wei Yan, Yongtao Xiao, Yunyi Zhang, Yijing Tao, Yi Cao, Kunhui Liu, Wei Cai, Ying Wang
Software Mentions: 1
Published: about 3 years ago
10.1111/jvim.15667
Congenital myasthenic syndrome in Golden Retrievers is associated with a novel <i>COLQ</i> mutationCited by: 1
Author(s): Kate L. Tsai, Karen M. Vernau, Kathryn Winger, Danielle M. Zwueste, Beverly K. Sturges, Marguerite F. Knipe, D. C. Williams, Kendall J. Anderson, Judith Evans, Ling Guo, Leigh Anne Clark, G. Diane Shelton
Software Mentions: 1
Published: about 5 years ago
10.1186/1479-5876-11-67
Significantly fewer protein functional changing variants for lipid metabolism in Africans than in EuropeansCited by: 4
Author(s): Xian Cheng, Xiaoming Liu, Yingyun Gong, Yuhai Zhao, Yun Xin Fu
Software Mentions: 1
Published: over 11 years ago
10.3390/nu6031115
Effect of the Novel Polysaccharide PolyGlycopleX® on Short-Chain Fatty Acid Production in a Computer-Controlled in Vitro Model of the Human Large IntestineCited by: 25
Author(s): Raylene A. Reimer, Annet Maathuis, Koen Venema, Michael R. Lyon, Roland J. Gahler, Simon Wood
Software Mentions: 1
Published: over 10 years ago
10.3390/nu12092607
Effectiveness of Protein Supplementation Combined with Resistance Training on Muscle Strength and Physical Performance in Elderly: A Systematic Review and Meta-AnalysisCited by: 16
Author(s): Noé Labata-Lezáun, Luis Llurda-Almuzara, Carlos López-de-Celis, Jacobo Rodríguez-Sanz, Vanessa González-Rueda, César Hidalgo-García, Borja Muñiz-Pardos, Albert Pérez‐Bellmunt
Software Mentions: 1
Published: over 4 years ago
10.1099/acmi.0.000012
Dwarfs in disguise: multiple spinal abscesses and spondylodiscitis caused by an Enterococcus faecium small-colony variantCited by: 2
Author(s): Steffen Höring, Katharina Sobotta, Sylke Schneider, Bettina Löffler, Jürgen Rödel
Software Mentions: 1
Published: almost 6 years ago
10.3390/nu10030369
Comprehensive Nutritional and Dietary Intervention for Autism Spectrum Disorder—A Randomized, Controlled 12-Month TrialCited by: 112
Author(s): James B. Adams, Tapan Audhya, E. Geis, Eva Gehn, Valeria Fimbres, Elena L. Pollard, Jessica Mitchell, Julie Ingram, Robert Hellmers, Dana Laake, Julie S. Matthews, Kefeng Li, Jane C. Naviaux, Robert K. Naviaux, Rebecca Adams, Devon M. Coleman, David Quig
Software Mentions: 1
Published: over 6 years ago
10.1002/advs.201801670
Metallization of 3D Printed Polymers and Their Application as a Fully Functional Water‐Splitting SystemCited by: 49
Author(s): Xiaoyang Su, Xinwei Li, Chun Yee Aaron Ong, Tun Seng Herng, Yanqing Wang, Erwin Peng, Jun Ding
Software Mentions: 1
Published: almost 6 years ago
10.1002/advs.201800397
Rapid Response Fluorescence Probe Enabled In Vivo Diagnosis and Assessing Treatment Response of Hypochlorous Acid‐Mediated Rheumatoid ArthritisCited by: 109
Author(s): Huan Feng, Zhiqiang Zhang, Qingtao Meng, Honglin Jia, Yue Wang, Run Zhang
Software Mentions: 1
Published: over 6 years ago
10.1002/ajmg.a.62337
Expanding the genetic landscape of oral‐facial‐digital syndrome with two novel genesCited by: 8
Author(s): Alanna Strong, Laurie Simone, Anthony D. Krentz, Courtney Vaccaro, Deborah Watson, Hayley A. Ron, Jennifer M. Kalish, Hélio Pedro, Elaine H. Zackai, Hákon Hákonarson
Software Mentions: 1
Published: over 3 years ago
10.1080/19768354.2017.1290678
Phenotypic and proteomic analysis of positively regulated gellan biosynthesis pathway in <i>Sphingomonas elodea</i>Cited by: 7
Author(s): Soo-Youn Lee, Ji‐Young Ahn, Mi-Hye Kim, Simranjeet Singh Sekhon, Sung–Jin Cho, Young-Chang Kim, Yang‐Hoon Kim
Software Mentions: 1
Published: almost 8 years ago
10.1002/acn3.51104
Accuracy of FGF‐21 and GDF‐15 for the diagnosis of mitochondrial disorders: A meta‐analysisCited by: 15
Author(s): Yan Lin, Kunqian Ji, Xinyan Ma, Shuangwu Liu, Wei Li, Yuying Zhao, Chuanzhu Yan
Software Mentions: 1
Published: over 4 years ago
10.1002/acn3.51050
VRK1 (Y213H) homozygous mutant impairs Cajal bodies in a hereditary case of distal motor neuropathyCited by: 8
Author(s): Ana T. Marcos, Elena Martín‐Doncel, Patricia Morejón‐García, Íñigo Marcos‐Alcalde, Paulino Gómez‐Puertas, María Segura‐Puimedon, Lluı́s Armengol, José M. Navarro‐Pando, Pedro A. Lazo
Software Mentions: 1
Published: over 4 years ago
10.1002/acn3.50895
Phenotypic variability of <i>GABRA1</i> ‐related epilepsy in monozygotic twinsCited by: 4
Author(s): Martin Krenn, Margot Ernst, Matthias Tomschik, Marco Treven, Matias Wagner, Dominik S. Westphal, Thomas Meitinger, Ekaterina Pataraia, Fritz Zimprich, Susanne Aull‐Watschinger
Software Mentions: 1
Published: about 5 years ago
10.1002/acn3.50868
Variants in <i>MME</i> are associated with autosomal‐recessive distal hereditary motor neuropathyCited by: 7
Author(s): Daojun Hong, Fang Pu, Sheng Yao, Juanjuan Chen, Xiaolei Zhang, Shuyun Chen, Jingfen Zhang, Dandan Tan, Li Wang, Xinsheng Han, Ling Xin, Yan Wang, Meige Liu, Lu Cong, Shanshan Zhong, Hui Ouyang, Xuguang Gao, Jun Zhang
Software Mentions: 1
Published: over 5 years ago
10.1002/acn3.51131
A novel hypomorphic splice variant in EIF2B5 gene is associated with mild ovarioleukodystrophyCited by: 3
Author(s): Agustí Rodríguez‐Palmero, Agatha Schlüter, Edgard Verdura, Montserrat Ruíz, Juan José Martínez, Isabelle Gourlaouen, Chandran Ka, Ricardo Lobato, Carlos Casasnovas, Gérald Le Gac, Stéphane Fourcade, Aurora Pujol
Software Mentions: 1
Published: over 4 years ago
10.1002/acn3.50967
A deep intronic splice variant advises reexamination of presumably dominant <i>SPG7</i> CasesCited by: 17
Author(s): Edgard Verdura, Agatha Schlüter, Gorka Fernández‐Eulate, Raquel Ramos‐Martín, Miren Zulaica, Laura Planas‐Serra, Montserrat Ruíz, Stéphane Fourcade, Carlos Casasnovas, Adolfo López de Munaín, Aurora Pujol
Software Mentions: 1
Published: almost 5 years ago
10.4103/0256-4947.75794
A rare human infection of <i>Raoultella ornithinolytica</i> in a diabetic foot lesionCited by: 27
Author(s): Yalçın Solak, Enes Elvin Gül, Hüseyin Atalay, Nejdet Genc, Halil Zeki Tonbul
Software Mentions: 1
Published: almost 14 years ago
10.5713/ajas.18.0122
In silico approaches to discover the functional impact of non-synonymous single nucleotide polymorphisms in selective sweep regions of the Landrace genomeCited by: 0
Author(s): Donghyun Shin, Kyung-Hye Won, Ki Duk Song
Software Mentions: 1
Published: about 6 years ago
10.1186/1471-2105-14-352
Status quo of annotation of human disease variantsCited by: 3
Author(s): Hanka Venselaar, Franscesca Camilli, Shima Gholizadeh, Marlou Snelleman, Han G. Brunner, Gert Vriend
Software Mentions: 1
Published: about 11 years ago
10.1186/s12859-019-2919-x
In silico analysis of missense mutations in exons 1–5 of the F9 gene that cause hemophilia BCited by: 8
Author(s): Lennon Meléndez-Aranda, Ana Rebeca Jaloma‐Cruz, Nina Pastor, Marina María de Jesús Romero-Prado
Software Mentions: 1
Published: over 5 years ago
10.1186/s12859-016-1436-4
GTB – an online genome tolerance browserCited by: 4
Author(s): Hashem A. Shihab, Mark F. Rogers, Michael Ferlaino, Colin Campbell, Tom R. Gaunt
Software Mentions: 1
Published: almost 8 years ago
10.1186/s12885-019-5307-z
Study protocol: a multi-centre randomised study of induction chemotherapy followed by capecitabine ± nelfinavir with high- or standard-dose radiotherapy for locally advanced pancreatic cancer (SCALOP-2)Cited by: 8
Author(s): Victoria Y Strauss, Rachel Shaw, P S Virdee, Chris Hurt, Elizabeth C. Ward, Bethan Tranter, Neel Patel, John Bridgewater, P Parsons, Ganesh Radhakrishna, Eric O’Neill, David Sebag‐Montefiore, M. Hawkins, Pippa Corrie, T Maughan, Somnath Mukherjee
Software Mentions: 1
Published: almost 6 years ago
10.1186/s12873-021-00472-w
Ultrasonography indicators for predicting difficult intubation: a systematic review and meta-analysisCited by: 22
Author(s): Mehran Sotoodehnia, Hosein Rafiemanesh, Hadi Mirfazaelian, Arash Safaie, Alireza Baratloo
Software Mentions: 1
Published: over 3 years ago
10.1186/s12902-020-00623-3
Differential diagnostic value of bilateral inferior Petrosal sinus sampling (BIPSS) in ACTH-dependent Cushing syndrome: a systematic review and Meta-analysisCited by: 15
Author(s): Hao Wang, Binwu Ying, Qinghe Xing, Rongrong Cai
Software Mentions: 1
Published: about 4 years ago
10.1186/s12863-019-0715-2
Subcongenic analysis of a quantitative trait locus affecting body weight and glucose metabolism in zinc transporter 7 (znt7)-knockout miceCited by: 2
Author(s): Liping Huang, Surapun Tepaamorndech, Catherine P. Kirschke, Yufeng Cai, Jun Zhao, Xiaohan Cao, Andrew Rao
Software Mentions: 1
Published: almost 6 years ago
10.1186/s12864-017-3913-1
Associating mutations causing cystinuria with disease severity with the aim of providing precision medicineCited by: 15
Author(s): Henry J Martell, Kathie Wong, J. Aragon Martin, Ziyan Kassam, Kay Thomas, Mark N. Wass
Software Mentions: 1
Published: over 7 years ago
10.1186/1471-2164-16-S10-S2
A comparative study of SVDquartets and other coalescent-based species tree estimation methodsCited by: 120
Author(s): Jed Chou, Ashu Gupta, Shashank Yaduvanshi, Ruth Davidson, Mike Nute, Siavash Mirarab, Tandy Warnow
Software Mentions: 1
Published: about 9 years ago
10.1186/s12864-017-3779-2
Blood meal induced regulation of the chemosensory gene repertoire in the southern house mosquitoCited by: 39
Author(s): Tanvi Taparia, Rickard Ignell, Sharon R. Hill
Software Mentions: 1
Published: over 7 years ago
10.1186/s12879-021-06064-0
Diagnostic value of neutrophil CD64, procalcitonin, and interleukin-6 in sepsis: a meta-analysisCited by: 31
Author(s): Shuang Cong, Tiangang Ma, Xin Di, Chang Tian, Min Zhao, Ke Wang
Software Mentions: 1
Published: over 3 years ago
10.1186/1471-2334-12-S2-S3
Therapeutic algorithms for chronic hepatitis C in the DAA era during the current economic crisis: whom to treat? How to treat? When to treat?Cited by: 10
Author(s): Salvatore Petta, Antonio Craxı̀
Software Mentions: 1
Published: about 12 years ago
10.1186/s12916-016-0574-x
Scandinavian guidelines for initial management of minor and moderate head trauma in childrenCited by: 59
Author(s): Ramona Åstrand, Christina Rosenlund, Johan Undén
Software Mentions: 1
Published: almost 9 years ago
10.1186/s12916-021-01940-7
Machine learning for subtype definition and risk prediction in heart failure, acute coronary syndromes and atrial fibrillation: systematic review of validity and clinical utilityCited by: 27
Author(s): Amitava Banerjee, Suliang Chen, Ghazaleh Fatemifar, Mohamad Zeina, R. Thomas Lumbers, Johanna Mielke, Simrat Gill, Dipak Kotecha, Daniel F. Freitag, Spiros Denaxas, Harry Hemingway
Software Mentions: 1
Published: over 3 years ago
10.1186/1471-2350-14-119
Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1genesCited by: 35
Author(s): Donia Elhayek, Gustavo Pérez de Nanclares, S. Chouchane, Saber Hamami, Adnène Mlika, Monia Troudi, Nadia Leban, Wafa Ben Romdane, M Gueddiche, Fethi Amri, Samir M’rabet, Jemni Ben Chibani, Luís Castaño, Amel Haj Khelil, Gema Ariceta
Software Mentions: 1
Published: about 11 years ago
10.1186/s12881-018-0555-3
Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysisCited by: 15
Author(s): Aparna Prasad, Matthew A. Sdano, Rena Vanzo, Patricia Mowery‐Rushton, Moises A. Serrano, Charles H. Hensel, E. Robert Wassman
Software Mentions: 1
Published: over 6 years ago
10.1186/s12881-019-0937-1
Identification of two novel COL10A1 heterozygous mutations in two Chinese pedigrees with Schmid-type metaphyseal chondrodysplasiaCited by: 5
Author(s): Lingchi Kong, Li Shi, Wenbo Wang, Rongtai Zuo, Mengwei Wang, Qinglin Kang
Software Mentions: 1
Published: about 5 years ago
10.1186/s12920-018-0353-y
Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnosticsCited by: 69
Author(s): Corinna Ernst, Eric Hahnen, Christoph Engel, Michael Nothnagel, Jonas Weber, Rita K. Schmutzler, Jan Hauke
Software Mentions: 1
Published: over 6 years ago
10.1186/s12866-018-1157-0
In silico comparative analysis of GGDEF and EAL domain signaling proteins from the Azospirillum genomesCited by: 13
Author(s): Alberto Ramírez Mata, César Millán Pacheco, José F. Cruz Pérez, Martha Minjárez Sáenz, Beatriz E. Baca
Software Mentions: 1
Published: over 6 years ago
10.1186/s12868-020-00591-3
Does conserved domain SOD1 mutation has any role in ALS severity and therapeutic outcome?Cited by: 3
Author(s): Surinder Pal, Abha Tiwari, Kaushal Sharma, Suresh Sharma
Software Mentions: 1
Published: about 4 years ago
10.1186/s12887-021-02922-7
Component of oligomeric Golgi complex 1 deficiency leads to hypoglycemia: a case report and literature reviewCited by: 1
Author(s): Yizhou Huang, Han Dai, Gangyi Yang, Lili Zhang, Shiyao Xue, Min Zhu
Software Mentions: 1
Published: about 3 years ago
10.1186/s12887-020-02097-7
Diagnostic test accuracy of new generation tympanic thermometry in children under different cutoffs: a systematic review and meta-analysisCited by: 1
Author(s): Dan Shi, Liyuan Zhang, Haixia Li
Software Mentions: 1
Published: over 4 years ago
10.1186/1471-2431-13-100
Performance of the pediatric index of mortality 2 (PIM-2) in cardiac and mixed intensive care units in a tertiary children’s referral hospital in ItalyCited by: 27
Author(s): Marta Luisa Ciofi degli Atti, Marina Cuttini, Lucilla Ravà, Silvia Rinaldi, Carla Brusco, Paola Cogo, Nicola Pirozzi, Sergio Picardo, Franco Schiavi, Massimiliano Raponi
Software Mentions: 1
Published: over 11 years ago
10.1186/1753-6561-5-S9-S13
Identification of functional genetic variation in exome sequence analysisCited by: 6
Author(s): Andrew E. Jaffe, Genevieve L. Wojcik, Audrey Y. Chu, Asieh Golozar, Ankit Maroo, Priya Duggal, Alison P. Klein
Software Mentions: 1
Published: about 13 years ago
10.1186/1753-6561-5-S9-S20
Incorporating predicted functions of nonsynonymous variants into gene-based analysis of exome sequencing data: a comparative studyCited by: 16
Author(s): Peng Wei, Xiaoming Liu, Yun Xin Fu
Software Mentions: 1
Published: about 13 years ago
10.1186/s12889-021-11603-0
A mysterious sensation about sleep and health: the role of interoceptionCited by: 3
Author(s): Teresa Arora, Mariapaola Barbato, Shaikha Al Hemeiri, Omar Omar, Maryam AlJassmi
Software Mentions: 1
Published: over 3 years ago
10.1186/s12890-020-01280-x
The meta-analysis for ideal cytokines to distinguish the latent and active TB infectionCited by: 10
Author(s): Zhenhong Wei, Yuanting Li, Chaojun Wei, Yonghong Li, Hui Xu, Yu Wu, Yanjuan Jia, Rui Guo, Jing Jia, Xiaoming Qi, Zhenhao Li, Xiaoling Gao
Software Mentions: 1
Published: about 4 years ago
10.1186/s12917-017-1184-3
Seasonal fluctuations in body weight during growth of Thoroughbred racehorses during their athletic careerCited by: 5
Author(s): Yuji Takahashi, Toshiyuki Takahashi
Software Mentions: 1
Published: over 7 years ago
10.1007/s00395-014-0451-8
FHL2 expression and variants in hypertrophic cardiomyopathyCited by: 51
Author(s): Felix W. Friedrich, Silke Reischmann, Aileen Schwalm, Andreas Unger, Deepak Ramanujam, Julia Münch, Oliver Müller, Christian Hengstenberg, Enrique Galve, Philippe Charron, Wolfgang A. Linke, Stefan Engelhardt, Monica Patten, Pascale Richard, Jolanda van der Velden, Thomas Eschenhagen, Richard Isnard, Lucie Carrier
Software Mentions: 1
Published: about 10 years ago
10.1155/2015/723682
Incidence and Prognostic Impact of<i>DNMT3A</i>Mutations in Korean Normal Karyotype Acute Myeloid Leukemia PatientsCited by: 6
Author(s): Sang Hyuk Park, Jae-Cheol Choi, Shine Young Kim, Jongyoun Yi, Seung Hwan Oh, In-Suk Kim, Hyung Hoi Kim, Chulhun L. Chang, Eun Yup Lee, Moo-Kon Song, Ho‐Jin Shin, Joo Seop Chung
Software Mentions: 1
Published: almost 10 years ago
10.1155/2015/798486
Impact of Dabigatran versus Phenprocoumon on ADP Induced Platelet Aggregation in Patients with Atrial Fibrillation with or without Concomitant Clopidogrel Therapy (the Dabi-ADP-1 and Dabi-ADP-2 Trials)Cited by: 15
Author(s): Amadea M. Martischnig, Julinda Mehilli, Janina Pollak, Tobias Petzold, Anette K. Fiedler, Katharina Mayer, Stefanie Schüpke, Dirk Sibbing, Steffen Maßberg, Adnan Kastrati, Nikolaus Sarafoff
Software Mentions: 1
Published: almost 10 years ago
10.1155/2013/517570
Novel<i>GUCA1A</i>Mutations Suggesting Possible Mechanisms of Pathogenesis in Cone, Cone-Rod, and Macular Dystrophy PatientsCited by: 24
Author(s): Kunka Kamenarova, Marta Cortón, Blanca García‐Sandoval, Patrícia José, Valentín Panchev, Almudena Ávila-Fernández, María Isabel López-Molina, Christina Chakarova, Carmen Ayuso, Shom Shanker Bhattacharya
Software Mentions: 1
Published: almost 12 years ago
10.1155/2018/7236194
Why They Are Different: Based on the Burden of Disease Research of WHO and Institute for Health Metrics and EvaluationCited by: 8
Author(s): Seok Jun Yoon, Young Eun Kim, Eun Jung Kim
Software Mentions: 1
Published: almost 7 years ago
10.3390/biomedicines9091167
Novel Mutations Detection with Next-Generation Sequencing and Its Association with Clinical Outcome in Unilateral Primary AldosteronismCited by: 7
Author(s): Che‐Hsiung Wu, Kang-Yung Peng, Daw-Yang Hwang, Yen-Hung Lin, Vin‐Cent Wu, Shih-Chieh Chueh
Software Mentions: 1
Published: about 3 years ago
10.1042/BSR20171300
Identification of a novel mutation in the <i>ABCA4</i> gene in a Chinese family with retinitis pigmentosa using exome sequencingCited by: 11
Author(s): Xiangjun Huang, Lamei Yuan, Hongbo Xu, Wen Zheng, Yanna Cao, Junhui Yi, Yi Guo, Zhijian Yang, Yu Li, Hao Deng
Software Mentions: 1
Published: over 6 years ago
10.1042/BSR20192235
A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosaCited by: 3
Author(s): Jiewen Fu, Jingliang Cheng, Qi Zhou, Chunli Wei, Hanchun Chen, Hongbin Lv, Junjiang Fu
Software Mentions: 1
Published: about 5 years ago
10.1097/MBC.0000000000000789
What concentration of tranexamic acid is needed to inhibit fibrinolysis? A systematic review of pharmacodynamics studiesCited by: 87
Author(s): Roberto Picetti, Haleema Shakur-Still, Robert L. Medcalf, Joseph F. Standing, Ian Roberts
Software Mentions: 1
Published: almost 6 years ago
10.1111/bjh.13563
<i>CSNK1A1</i> mutations and gene expression analysis in myelodysplastic syndromes with del(5q)Cited by: 18
Author(s): Erica Bello, Andrea Pellagatti, Jacqueline Shaw, Cristina Mecucci, Rajko Kušec, Sally Killick, Aristoteles Giagounidis, Sophie Raynaud, Marı́a José Calasanz, Pierre Fenaux, Jacqueline Boultwood
Software Mentions: 1
Published: over 9 years ago
10.1002/brb3.1066
A novel SETX gene mutation associated with Juvenile amyotrophic lateral sclerosisCited by: 12
Author(s): Limin Ma, Yingying Shi, Zhongcan Chen, Shujian Li, Jiewen Zhang
Software Mentions: 1
Published: over 6 years ago
10.1002/brb3.1724
A novel <i>TFG</i> c.793C>G mutation in a Chinese pedigree with Charcot‐Marie‐Tooth disease 2Cited by: 3
Author(s): Dingwen Wu, Yanfang Li, Xinzhen Yin, Baorong Zhang
Software Mentions: 1
Published: over 4 years ago
10.21470/1678-9741-2018-0234
Diagnostic Performance of QFR for the Evaluation of Intermediate Coronary Artery Stenosis Confirmed by Fractional Flow ReserveCited by: 9
Author(s): Zhenhua Xing, Junyu Pei, Jinbo Huang, Xinqun Hu, Shan Gao
Software Mentions: 1
Published: almost 6 years ago
10.1111/cns.13456
Variants of genes encoding TNF receptors and ligands and proteins regulating TNF activation in familial multiple sclerosisCited by: 3
Author(s): Laura Torre‐Fuentes, Jordi A. Matías‐Guiu, Vanesa Pytel, Paloma Montero‐Escribano, Paolo Maietta, Sara Álvarez, Ulises Gómez‐Pinedo
Software Mentions: 1
Published: about 4 years ago
10.1111/cns.13284
New clinical characteristics and novel pathogenic variants of patients with hereditary leukodystrophiesCited by: 6
Author(s): Juan‐Juan Xie, Ni Wang, Qiao Wei, Hongxia Ma, Ge Bai, Ying Shen, Zhi‐Ying Wu
Software Mentions: 1
Published: almost 5 years ago