Ecosyste.ms: Papers

10.3389/fmicb.2020.00711

Population Genomics of Mycobacterium leprae Reveals a New Genotype in Madagascar and the Comoros
Cited by: 11
Author(s): Charlotte Avanzi, Emmanuel Lecorché, Fetra Angelot Rakotomalala, Andrej Benjak, F. Rapelanoro Rabenja, Lala Soavina Ramarozatovo, B. Cauchoix, Mala Rakoto-Andrianarivelo, Maria Tió-Coma, Thyago Leal-Calvo, Philippe Busso, Stefanie Boy‐Röttger, Aurélie Chauffour, T Rasamoelina, Aina Andrianarison, Fandresena Arilala Sendrasoa, John S. Spencer, Pushpendra Singh, Digambar Dashatwar, Rahul Narang, Jean-Luc Berland, Vincent Jarlier, Cláudio Guedes Salgado, Milton Ozório Moraes, Annemieke Geluk, Andriamira Randrianantoandro, Emmanuelle Cambau, Stewart T. Cole
Software Mentions: 3
Published: over 4 years ago

10.3389/fped.2019.00122

Combined Immunodeficiency With Late-Onset Progressive Hypogammaglobulinemia and Normal B Cell Count in a Patient With RAG2 Deficiency
Cited by: 10
Author(s): Mayra B. Dorna, Pamela F. A. Barbosa, A. Rangel-Santos, Krisztián Csomós, Boglárka Ujházi, Joseph Dasso, D.I. Thwaites, Joan Boyes, Sinisa Savic, Jolán E. Walter
Software Mentions: 3
Published: over 5 years ago

10.3389/fpls.2019.01514

Genome-Wide Comparisons of Mutations Induced by Carbon-Ion Beam and Gamma-Rays Irradiation in Rice via Resequencing Multiple Mutants
Cited by: 23
Author(s): Gangyi Yang, Wenlong Luo, Jian Zhang, Xian-cheng Yan, Yuguo Du, Libin Zhou, Wenjian Li, Hui Wang, Zhiqiang Chen, Tao Guo
Software Mentions: 3
Published: almost 5 years ago

10.1038/s41436-020-01071-z

A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy
Cited by: 9
Author(s): Min Ni, Bushra Afroze, Chao Xing, Chunxiao Pan, Yanqiu Shao, Ling Cai, Brandi L. Cantarel, Jimin Pei, Nick V. Grishin, Stacy Hewson, Devon Knight, Sonal Mahida, Donnice Michel, Mark A. Tarnopolsky, Annapurna Poduri, Alexander Rotenberg, Neal Sondheimer, Ralph J. DeBerardinis
Software Mentions: 3
Published: over 3 years ago

10.1093/gbe/evab126

The Assembled and Annotated Genome of the Fairy-Ring Fungus <i>Marasmius oreades</i>
Cited by: 9
Author(s): Markus Hiltunen, Sandra Lorena Ament‐Velásquez, Hanna Johannesson
Software Mentions: 3
Published: over 3 years ago

10.1186/s13073-015-0195-6

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting
Cited by: 49
Author(s): Márton Münz, Elise Ruark, Anthony Renwick, Emma Ramsay, Matthew Clarke, Shazia Mahamdallie, Victoria Cloke, Sheila Seal, Ann Strydom, Gerton Lunter, Nazneen Rahman
Software Mentions: 3
Published: over 9 years ago

10.1186/s13073-015-0251-2

ScanIndel: a hybrid framework for indel detection via gapped alignment, split reads and de novo assembly
Cited by: 39
Author(s): Rendong Yang, Andrew C. Nelson, Christine Henzler, Bharat Thyagarajan, Kevin A.T. Silverstein
Software Mentions: 3
Published: almost 9 years ago

10.1186/s13073-018-0529-2

From somatic variants towards precision oncology: Evidence-driven reporting of treatment options in molecular tumor boards
Cited by: 32
Author(s): Júlia Perera-Bel, Barbara Hutter, Christoph Heining, Annalen Bleckmann, Martina Fröhlich, Stefan Fröhling, Hanno Glimm, Benedikt Brors, Tim Beißbarth
Software Mentions: 3
Published: over 6 years ago

10.1186/s13073-018-0606-6

Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing
Cited by: 102
Author(s): Alba Sanchis‐Juan, Jonathan Stephens, Courtney French, Nicholas Gleadall, Karyn Mégy, Christopher J. Penkett, Olga Shamardina, Kathleen Stirrups, Isabelle Delon, Eleanor Dewhurst, Helen Dolling, Marie Erwood, Detelina Grozeva, Luca Stefanucci, Gavin Arno, Andrew R. Webster, Trevor Cole, Topun Austin, Ricardo Garcia Branco, Willem H. Ouwehand, F. Lucy Raymond, Keren Carss
Software Mentions: 3
Published: almost 6 years ago

10.1093/gigascience/giz074

Identifying, understanding, and correcting technical artifacts on the sex chromosomes in next-generation sequencing data
Cited by: 57
Author(s): Timothy H. Webster, Madeline Couse, Bruno M. Grande, Eric Karlins, Tanya N. Phung, Phillip A. Richmond, Whitney Whitford, Melissa A. Wilson
Software Mentions: 3
Published: over 5 years ago

10.3390/healthcare9070792

Post-Analysis of Predictive Modeling with an Epidemiological Example
Cited by: 0
Author(s): Christina Brester, Ari Voutilainen, Tomi‐Pekka Tuomainen, Jussi Kauhanen, Mikko Kolehmainen
Software Mentions: 3
Published: over 3 years ago

10.1007/s10875-021-01050-2

Decreased ATM Function Causes Delayed DNA Repair and Apoptosis in Common Variable Immunodeficiency Disorders
Cited by: 6
Author(s): Chantal E. Hargreaves, Silvia Salatino, Sarah C. Sasson, James E.G. Charlesworth, Elizabeth Bateman, Arzoo Patel, Consuelo Anzilotti, John Broxholme, Julian C. Knight, Smita Y. Patel
Software Mentions: 3
Published: over 3 years ago

10.1002/jcc.24318

Development of massive multilevel molecular dynamics simulation program, platypus (PLATform for dYnamic protein unified simulation), for the elucidation of protein functions
Cited by: 5
Author(s): Yu Takano, Kazuto Nakata, Yasushige Yonezawa, Haruki Nakamura
Software Mentions: 3
Published: over 8 years ago

10.1038/srep14283

SeqMule: automated pipeline for analysis of human exome/genome sequencing data
Cited by: 56
Author(s): Yunfei Guo, Xiaolei Ding, Yufeng Shen, Gholson J. Lyon, Kai Wang
Software Mentions: 3
Published: about 9 years ago

10.1038/srep31029

OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis
Cited by: 10
Author(s): Elise Ruark, Márton Münz, Matthew Clarke, Anthony Renwick, Emma Ramsay, Anna Elliott, Sheila Seal, Gerton Lunter, Nazneen Rahman
Software Mentions: 3
Published: over 8 years ago

10.1038/s41598-018-20783-6

The impact of reconstructed soils following oil sands exploitation on aspen and its associated belowground microbiome
Cited by: 12
Author(s): Franck Stefani, Nathalie Isabel, Marie-Josée Morency, Manuel Lamothe, Simon Nadeau, Denis Lachance, Edith H.Y. Li, Charles W. Greer, Étienne Yergeau, Bradley D. Pinno, Armand Séguin
Software Mentions: 3
Published: almost 7 years ago

10.1038/s41598-019-39108-2

Comparative analysis of whole-genome sequencing pipelines to minimize false negative findings
Cited by: 54
Author(s): Kyu-Baek Hwang, In‐Hee Lee, Honglan Li, Dhong-Geon Won, Carles Hernandez‐Ferrer, Jose A. Negron, Sek Won Kong
Software Mentions: 3
Published: over 5 years ago

10.1038/s41598-019-47405-z

Uncovering missed indels by leveraging unmapped reads
Cited by: 8
Author(s): Mohammad Shabbir Hasan, Xiaowei Wu, Liqing Zhang
Software Mentions: 3
Published: over 5 years ago

10.1186/s40246-019-0194-6

vi-HMM: a novel HMM-based method for sequence variant identification in short-read data
Cited by: 1
Author(s): Man Lai Tang, Mohammad Shabbir Hasan, Hongxiao Zhu, Liqing Zhang, Xiaowei Wu
Software Mentions: 3
Published: almost 6 years ago

10.1093/hmg/ddv182

Mutations in the PP2A regulatory subunit B family genes<i>PPP2R5B</i>,<i>PPP2R5C</i>and<i>PPP2R5D</i>cause human overgrowth
Cited by: 68
Author(s): Chey Loveday, Katrina Tatton‐Brown, Matthew Clarke, Isaac M. Westwood, Anthony Renwick, Emma Ramsay, Andrea H. Németh, Jennifer Campbell, Shelagh Joss, McKinlay Gardner, Anna Zachariou, Anna Elliott, Elise Ruark, Rob van Montfort, Nazneen Rahman
Software Mentions: 3
Published: over 9 years ago

10.3390/ijms22041837

Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer
Cited by: 5
Author(s): Diamanto Skopelitou, Benchun Miao, Aayushi Srivastava, Abhishek Kumar, Magdalena Kuswick, Dagmara Dymerska, Nagarajan Paramasivam, Matthias Schlesner, Jan Lubiński, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
Software Mentions: 3
Published: almost 4 years ago

10.18632/oncotarget.26400

Clinical impact of measurable residual disease monitoring by ultradeep next generation sequencing in <i>NPM1</i> mutated acute myeloid leukemia
Cited by: 24
Author(s): Nikhil Patkar, Rohan Kodgule, Chinmayee Kakirde, Goutham Raval, Prasanna Bhanshe, Shalik Ram Joshi, Shruti Chaudhary, Yajamanam Badrinath, Sitaram Ghoghale, Shraddha Kadechkar, Syed Hasan Khizer, Sadhana Kannan, Dhanalaxmi Shetty, Anant Gokarn, Sachin Punatkar, Hasmukh Jain, Bhausaheb Bagal, Hari Menon, Manju Sengar, Navin Khattry, Prashant Tembhare, Papagudi Ganesan Subramanian, Sumeet Gujral
Software Mentions: 3
Published: almost 6 years ago

10.3390/jpm11040262

A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer
Cited by: 0
Author(s): Diamanto Skopelitou, Benchun Miao, Aayushi Srivastava, Abhishek Kumar, Magdalena Kuświk, Dagmara Dymerska, Nagarajan Paramasivam, Matthias Schlesner, Jan Lubiński, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
Software Mentions: 3
Published: over 3 years ago

10.3389/fendo.2021.660731

Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes
Cited by: 4
Author(s): Birgit Weiß, Birgit Eberle, Ralph Roeth, Christiaan de Bruin, Julian C. Lui, Nagarajan Paramasivam, Katrin Hinderhofer, Hermine A. van Duyvenvoorde, Jeffrey Baron, Jan M. Wit, Gudrun Rappold
Software Mentions: 2
Published: over 3 years ago

10.3389/fgene.2021.741355

Novel Hemizygous Mutations of TEX11 Cause Meiotic Arrest and Non-obstructive Azoospermia in Chinese Han Population
Cited by: 7
Author(s): Zhiyong Ji, Chencheng Yao, Chao Yang, Chuan Huang, Liangyu Zhao, Xiaodong Han, Zijue Zhu, Erlei Zhi, Nachuan Liu, Zhi Zhou, Zheng Li
Software Mentions: 2
Published: about 3 years ago

10.3389/fgene.2019.00093

Insights Into an Unexplored Component of the Mosquito Repeatome: Distribution and Variability of Viral Sequences Integrated Into the Genome of the Arboviral Vector Aedes albopictus
Cited by: 19
Author(s): Elisa Pischedda, Francesca Scolari, Federica Valerio, Rebeca Carballar-Lejarazú, Paolo Luigi Catapano, Robert M. Waterhouse, Mariangela Bonizzoni
Software Mentions: 2
Published: almost 6 years ago

10.1038/s41598-020-61695-8

Genetic landscape of autism spectrum disorder in Vietnamese children
Cited by: 11
Author(s): Kien Trung Tran, Vinh Sy Le, Hoa Thi Phuong Bui, Huy Duong, Ha Thi Thanh Ly, Hieu Nguyen, Lan T M Dao, Thanh H. Nguyen, Duc Vu, Lien Thi Ha, Hanh N. D. Le, Arijit Mukhopadhyay, Liem Thanh Nguyen
Software Mentions: 2
Published: over 4 years ago

10.3389/fgene.2020.00415

Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India
Cited by: 17
Author(s): Arshia Angural, Akshi Spolia, Ankit Mahajan, Vivek Verma, Ankush Sharma, Parvinder Kumar, Manoj K. Dhar, Kamal Kishore Pandita, Ekta Rai, Swarkar Sharma
Software Mentions: 2
Published: over 4 years ago

10.3389/fgene.2015.00311

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability
Cited by: 35
Author(s): Majida Charif, Agathe Roubertie, Sara Salime, Sonia Mamouni, Cyril Goizet, Christian Hamel, Guy Lenaers
Software Mentions: 2
Published: about 9 years ago

10.3892/mmr.2019.10464

Identification of a novel mutation site in maturity‑onset diabetes of the young in a Chinese family by whole‑exome sequencing
Cited by: 3
Author(s): Yu Han, Jingjin Liu, Xiaofei Li, Fang Miao, Yanlan Yang
Software Mentions: 2
Published: over 5 years ago

10.1002/mgg3.885

Identification of a novel EVC variant in a Han‐Chinese family with Ellis‐van Creveld syndrome
Cited by: 3
Author(s): Xiangjun Huang, Yi Guo, Hongbo Xu, Zhijian Yang, Xiong Deng, Hao Deng, Lamei Yuan
Software Mentions: 2
Published: over 5 years ago

10.1186/s12915-015-0152-2

Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits
Cited by: 47
Author(s): Yu Huang, Vasily Ramensky, Susan Service, Anna J. Jasinska, Yoon Jung, Oi-Wa Choi, Rita M. Cantor, Nikoleta Juretic, Jessica Wasserscheid, Jay R. Kaplan, Matthew J. Jorgensen, Thomas D. Dyer, Ken Dewar, John Blangero, Richard K. Wilson, Wesley C. Warren, George M. Weinstock, Nelson B. Freimer
Software Mentions: 2
Published: over 9 years ago

10.1186/s13100-016-0076-6

Evidence for L1-associated DNA rearrangements and negligible L1 retrotransposition in glioblastoma multiforme
Cited by: 30
Author(s): Patricia E. Carreira, Adam D. Ewing, Guibo Li, Stephanie N. Schauer, Kyle R. Upton, Allister C. Fagg, Santiago Morell, Michaela Kindlova, Patricia Gerdes, Sandra R. Richardson, Bo Li, Daniel J. Gerhardt, Jun Wang, Paul M. Brennan, Geoffrey J. Faulkner
Software Mentions: 2
Published: about 8 years ago

10.1038/s41598-021-85354-8

Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Cited by: 12
Author(s): Hannah Roberts, Maria Lopopolo, Alistair T. Pagnamenta, Eshita Sharma, Duncan Parkes, Lorne Lonie, Colin Freeman, Samantha J. L. Knight, Gerton Lunter, Hélène Dreau, Helen Lockstone, Jenny C. Taylor, Anna Schuh, Rory Bowden, David Buck
Software Mentions: 2
Published: over 3 years ago

10.3389/fmicb.2020.01220

Genomic Characterization of Mycobacterium leprae to Explore Transmission Patterns Identifies New Subtype in Bangladesh
Cited by: 17
Author(s): Maria Tió-Coma, Charlotte Avanzi, Els M. Verhard, Louise Pierneef, Anouk van Hooij, Andrej Benjak, Johan Chandra Roy, Marufa Khatun, Khorshed Alam, Paul L. A. M. Corstjens, Stewart T. Cole, Jan Hendrik Richardus, Annemieke Geluk
Software Mentions: 2
Published: over 4 years ago

10.1186/1471-2105-7-424

PubFocus: semantic MEDLINE/PubMed citations analytics through integration of controlled biomedical dictionaries and ranking algorithm
Cited by: 53
Author(s): Maksim V. Plikus, Zina Zhang, Cheng‐Ming Chuong
Software Mentions: 2
Published: about 18 years ago

10.3389/fneur.2021.602979

Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic Neuropathy
Cited by: 11
Author(s): Majida Charif, Céline Bris, David Goudenège, Valérie Desquiret-Dumas, Estelle Colin, Alban Ziegler, Vincent Procaccio, Pascal Reynier, Dominique Bonneau, Guy Lenaers, Patrizia Amati‐Bonneau
Software Mentions: 2
Published: over 3 years ago

10.3389/fnins.2019.01135

Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients
Cited by: 33
Author(s): Ana Fernández–Marmiesse, Iria Roca, Felicitas Díaz‐Flores, Verónica Cantarín, Ma Socorro Pérez-Poyato, Ana Fontalba, Francisco Laranjeira, Sofia Quintans, Oana Moldovan, Blanca Felgueroso, Montserrat Rodríguez-Pedreira, Rogelio Simón, Ana Camacho, Pilar Quijada, Salvador Ibáñez-Micó, Ma Rosario Domingno, Carmen Benito, Rocío Velasco Calvo, Antonia Pérez-Cejas, Ma Llanos Carrasco, Feliciano J. Ramos, Ma Luz Couce, M.L. Ruiz-Falcó, Luis González Gutiérrez-Solana, Margarita Martínez-Atienza
Software Mentions: 2
Published: about 5 years ago

10.3389/fped.2020.00145

GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children
Cited by: 3
Author(s): Petra Loid, Minna Pekkinen, Monica Reyes, Taina Mustila, Heli Viljakainen, Harald Jüppner, Outi Mäkitie
Software Mentions: 2
Published: over 4 years ago

10.1186/s13044-019-0069-x

Meeting Abstracts from the 67th Annual British Thyroid Association Meeting
Cited by: 1
Author(s):
Software Mentions: 2
Published: about 5 years ago

10.1128/mBio.00696-16

Mutations in the Plasmodium falciparum Cyclic Amine Resistance Locus (PfCARL) Confer Multidrug Resistance
Cited by: 39
Author(s): Gregory LaMonte, Michelle Yi-Xiu Lim, Melanie Wree, Christin Reimer, Marie Nachon, Victoria C. Corey, Peter Gedeck, David Plouffe, Alan Y. Du, N Varela Figueroa, Bryan K. S. Yeung, Pablo Bifani, Elizabeth A. Winzeler
Software Mentions: 2
Published: about 8 years ago

10.1534/g3.118.200263

Insights into the Structure of the Spruce Budworm (<i>Choristoneura fumiferana</i>) Genome, as Revealed by Molecular Cytogenetic Analyses and a High-Density Linkage Map
Cited by: 12
Author(s): Sandrine Picq, Lisa M. Lumley, Jindra Šíchová, Jérôme Laroche, Esther Pouliot, Bryan M. T. Brunet, Roger C. Levesque, Felix A. H. Sperling, František Marec, Michel Cusson
Software Mentions: 2
Published: over 6 years ago

10.1016/j.ccell.2018.03.013

The Origins and Vulnerabilities of Two Transmissible Cancers in Tasmanian Devils
Cited by: 83
Author(s): Maximilian R Stammnitz, Tim Coorens, Kevin Gori, Dane Hayes, Beiyuan Fu, Jinhong Wang, Daniel E. Martin‐Herranz, Ludmil B. Alexandrov, Adrian Baez‐Ortega, Syd Barthorpe, Alexandra Beck, Francesca Giordano, Graeme Knowles, Young Mi Kwon, George T. Hall, Stacey Price, Ruth J. Pye, José M. C. Tubío, Hannah V. Siddle, Sukhwinder Singh Sohal, Gregory M. Woods, Ultan McDermott, Fengtang Yang, Mathew J. Garnett, Zemin Ning, Elizabeth P. Murchison
Software Mentions: 2
Published: over 6 years ago

10.1093/braincomms/fcab036

A novel remitting leukodystrophy associated with a variant in FBP2
Cited by: 1
Author(s): Agnieszka Gizak, Susann Diegmann, Steffi Dreha-Kulaczewski, J. Wisniewski, Przemysław Duda, Andreas Ohlenbusch, Brenda Huppke, Marco Henneke, Wolfgang Höhne, Janine Altmüller, Holger Thiele, Peter Nürnberg, Dariusz Rakus, Jutta Gärtner, Peter Huppke
Software Mentions: 2
Published: over 3 years ago

10.3390/genes11121497

Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKL
Cited by: 3
Author(s): Susan M. Downes, Tham Thi Nguyen, Vicky Tai, Suzanne Broadgate, Mital Shah, Saoud Al‐Khuzaei, Robert E. MacLaren, Morag Shanks, Penny Clouston, Stephanie Halford
Software Mentions: 2
Published: almost 4 years ago

10.1093/brain/awz342

A causal role for TRESK loss of function in migraine mechanisms
Cited by: 44
Author(s): Philippa Pettingill, Greg A. Weir, Tina Wei, Yukyee Wu, Grace Flower, Tatjana Lalic, Adam E. Handel, Galbha Duggal, Satyan Chintawar, Jonathan Cheung, Kanisa Arunasalam, Elizabeth Couper, Larisa M. Haupt, Lyn R. Griffiths, Andrew Bassett, Sally A. Cowley, M Z Cader
Software Mentions: 2
Published: about 5 years ago

10.3390/genes12040508

Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
Cited by: 5
Author(s): Hwei Wuen Chan, Elena R. Schiff, Vijay Tailor, Samantha Malka, M. Neveu, Maria Theodorou, Mariya Moosajee
Software Mentions: 2
Published: over 3 years ago

10.1038/s41408-019-0243-3

Identification of new putative driver mutations and predictors of disease evolution in chronic lymphocytic leukemia
Cited by: 2
Author(s): Adrián Mosquera Orgueira, Beatriz Antelo Rodríguez, José Ángel Díaz Arias, José Luis Bello López
Software Mentions: 2
Published: about 5 years ago

10.1186/1471-2105-15-63

Identification of pathogen genomic variants through an integrated pipeline
Cited by: 45
Author(s): Micah J Manary, Suriya S Singhakul, Erika L. Flannery, Selina Bopp, Victoria C. Corey, A. Taylor Bright, Case W. McNamara, John R. Walker, Elizabeth A. Winzeler
Software Mentions: 2
Published: over 10 years ago

10.3390/biom9100605

Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways
Cited by: 22
Author(s): Aayushi Srivastava, Abhishek Kumar, Sara Galimberti, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
Software Mentions: 2
Published: about 5 years ago

10.1186/s13059-019-1709-0

Haplotype-aware diplotyping from noisy long reads
Cited by: 39
Author(s): Jana Ebler, Marina Haukness, Trevor Pesout, Tobias Marschall, Benedict Paten
Software Mentions: 2
Published: over 5 years ago

10.3390/biology6010021

SNP Discovery Using a Pangenome: Has the Single Reference Approach Become Obsolete?
Cited by: 68
Author(s): Bhavna Hurgobin, David Edwards
Software Mentions: 2
Published: over 7 years ago

10.1242/bio.201410116

Genetic interaction implicates iRhom2 in the regulation of EGF receptor signalling in mice
Cited by: 29
Author(s): Owen M. Siggs, Adam G. Grieve, Hongmei Xu, Paul Bambrough, Yonka Christova, Matthew Freeman
Software Mentions: 2
Published: about 10 years ago

10.18632/oncotarget.15874

Search for rare protein altering variants influencing susceptibility to multiple myeloma
Cited by: 11
Author(s): Matthew Scales, Daniel Chubb, Sara E. Dobbins, David C. Johnson, Ni Li, Michael J.E. Sternberg, Neils Weinhold, Caleb K. Stein, Graham Jackson, Faith E. Davies, Brian A. Walker, Christopher P. Wardell, Richard S. Houlston, Gareth J. Morgan
Software Mentions: 2
Published: over 7 years ago

10.1186/gm543

Choice of transcripts and software has a large effect on variant annotation
Cited by: 154
Author(s): Davis J. McCarthy, Peter Humburg, Alexander Kanapin, Manuel A. Rivas, Kyle J. Gaulton, Jean‐Baptiste Cazier, Peter Donnelly
Software Mentions: 2
Published: almost 11 years ago

10.1186/s13073-014-0073-7

Whole-genome haplotyping approaches and genomic medicine
Cited by: 61
Author(s): Gustavo Glusman, Hannah Cox, Jared C. Roach
Software Mentions: 2
Published: about 10 years ago

10.1186/s12859-018-2147-9

A study on fast calling variants from next-generation sequencing data using decision tree
Cited by: 13
Author(s): Zhentang Li, Yi Wang, Fei Wang
Software Mentions: 2
Published: over 6 years ago

10.1093/hmg/ddv117

Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis
Cited by: 49
Author(s): Alistair T. Pagnamenta, Malcolm F. Howard, Éva Wisniewski, Niko Popitsch, Samantha J. L. Knight, David A. Keays, Gerardine Quaghebeur, Helen Cox, Phillip Cox, Tamás Balla, Jenny C. Taylor, Usha Kini
Software Mentions: 2
Published: over 9 years ago

10.1186/s13073-016-0269-0

Medical implications of technical accuracy in genome sequencing
Cited by: 107
Author(s): Rachel L. Goldfeder, James R. Priest, Justin M. Zook, Megan E. Grove, Daryl Waggott, Matthew T. Wheeler, Marc Salit, Euan A. Ashley
Software Mentions: 2
Published: over 8 years ago

10.1016/j.ajhg.2018.08.013

Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency
Cited by: 39
Author(s): Charlotte L. Alston, Juliana Heidler, Marris G. Dibley, Laura S. Kremer, Lucie S. Taylor, Carl Fratter, Courtney French, Ruth I.C. Glasgow, René G. Feichtinger, Isabelle Delon, Alistair T. Pagnamenta, Helen Dolling, Hugh Lemonde, Neil Aiton, Alf Bjørnstad, Lisa Henneke, Jutta Gärtner, Holger Thiele, Kateřina Tauchmannová, Gerardine Quaghebeur, Josef Houštěk, Wolfgang Sperl, F. Lucy Raymond, Holger Prokisch, Johannes A. Mayr, Robert McFarland, Joanna Poulton, Michael Ryan, Ilka Wittig, Marco Henneke, Robert W. Taylor
Software Mentions: 2
Published: about 6 years ago

10.1093/bioinformatics/btv654

Comparison of genetic variants in matched samples using thesaurus annotation
Cited by: 4
Author(s): Tomasz Konopka, Sebastian M. Nijman
Software Mentions: 2
Published: about 9 years ago

10.1093/hmg/ddu030

Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis
Cited by: 207
Author(s): Hilary C. Martin, Grace Kim, Alistair T. Pagnamenta, Yoshiko Murakami, Gemma L. Carvill, Esther Meyer, Richard R. Copley, Andrew Rimmer, Giulia Barcia, Matthew R Fleming, Jack Kronengold, Maile R. Brown, Karl A. Z. Hudspith, John Broxholme, Alexander Kanapin, Jean‐Baptiste Cazier, Taroh Kinoshita, Rima Nabbout, David Bentley, Gil McVean, Sinéad B. Heavin, Zenobia Zaiwalla, Tony McShane, Heather C Mefford, Deborah Shears, Helen Stewart, Manju A. Kurian, Ingrid E. Scheffer, Edward Blair, Peter Donnelly, Leonard K. Kaczmarek, Jenny C. Taylor
Software Mentions: 2
Published: almost 11 years ago

10.1186/s12870-018-1537-5

QTL mapping of melon fruit quality traits using a high-density GBS-based genetic map
Cited by: 76
Author(s): Lara Pereira, Valentino Ruggieri, Salvador Pérez, Konstantinos G. Alexiou, M. Fernández, Torben Jahrmann, Marta Pujol, Jordi García-Más
Software Mentions: 2
Published: almost 6 years ago

10.1186/s12920-020-00818-6

Comparative assessments of indel annotations in healthy and cancer genomes with next-generation sequencing data
Cited by: 5
Author(s): Jing Chen, Jun‐tao Guo
Software Mentions: 2
Published: about 4 years ago

10.1093/hmg/ddx270

A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability
Cited by: 28
Author(s): Benjamin Davies, L. M. Brown, Ondřej Cais, Jake F. Watson, Amber J. Clayton, Veronica T. Chang, David F. Biggs, Chris Preece, Polinka Hernandez-Pliego, J Krohn, Amarjit Bhomra, Stephen R.F. Twigg, Andrew Rimmer, Alexander Kanapin, Arjune Sen, Zenobia Zaiwalla, Gil McVean, Russell G. Foster, Peter Donnelly, Jenny C. Taylor, Edward Blair, David Nutt, A. Radu Aricescu, Ingo H. Greger, Stuart N. Peirson, Jonathan Flint, Hilary C. Martin
Software Mentions: 2
Published: over 7 years ago

10.1186/s12920-018-0342-1

EAGLE: Explicit Alternative Genome Likelihood Evaluator
Cited by: 12
Author(s): Tony Kuo, Martin C. Frith, Jun Sese, Paul Horton
Software Mentions: 2
Published: over 6 years ago

10.1002/humu.23598

Disruption of<i>TWIST1</i>translation by 5′ UTR variants in Saethre-Chotzen syndrome
Cited by: 10
Author(s): Yan Zhou, Nils Koelling, Aimée L. Fenwick, Simon J. McGowan, Eduardo Calpena, Steven A. Wall, Sarah Smithson, Andrew O.M. Wilkie, Stephen R.F. Twigg
Software Mentions: 2
Published: over 6 years ago

10.1186/s13053-021-00167-0

A rare large duplication of MLH1 identified in Lynch syndrome
Cited by: 2
Author(s): Abhishek Kumar, Nagarajan Paramasivam, Obul Reddy Bandapalli, Matthias Schlesner, Tianhui Chen, Rolf H. Sijmons, Dagmara Dymerska, Katarzyna Gołębiewska, Magdalena Kuświk, Jan Lubiński, Kari Hemminki, Asta Försti
Software Mentions: 2
Published: almost 4 years ago

10.1186/s13053-016-0058-1

Pedigree based DNA sequencing pipeline for germline genomes of cancer families
Cited by: 6
Author(s): Asta Försti, Abhishek Kumar, Nagarajan Paramasivam, Matthias Schlesner, Calogerina Catalano, Dagmara Dymerska, Jan Lubiński, Roland Eils, Kari Hemminki
Software Mentions: 2
Published: over 8 years ago

10.1001/jamanetworkopen.2019.5752

Clinical and Molecular Characterization of<i>PROM1</i>-Related Retinal Degeneration
Cited by: 35
Author(s): Jasmina Cehajic-Kapetanovic, Johannes Birtel, Michelle E. McClements, Morag Shanks, Penny Clouston, Susan M. Downes, Peter Charbel Issa, Robert E. MacLaren
Software Mentions: 2
Published: over 5 years ago

10.1007/s10858-017-0136-3

Methyl group assignment using pseudocontact shifts with PARAssign
Cited by: 24
Author(s): Mathilde Lescanne, Simon P. Skinner, Anneloes Blok, Monika Timmer, Linda Cerofolini, Marco Fragai, Claudio Luchinat, Marcellus Ubbink
Software Mentions: 2
Published: almost 7 years ago

10.1002/jbmr.2797

Identification of a G‐Protein Subunit‐α11 Gain‐of‐Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)
Cited by: 33
Author(s): Siân E. Piret, Caroline M Gorvin, Alistair T. Pagnamenta, Sarah Howles, Treena Cranston, Nigel Rust, M. Andrew Nesbit, Benjamin Gläser, Jenny C. Taylor, Andreas Buchs, Fadil Hannan
Software Mentions: 2
Published: over 8 years ago

10.1186/s13046-019-1248-2

Colorectal cancer-derived extracellular vesicles induce transformation of fibroblasts into colon carcinoma cells
Cited by: 35
Author(s): Mohamed Abdouh, Matteo Floris, Zu‐Hua Gao, Vincenzo Arena, Manuel Arena, Goffredo Arena
Software Mentions: 2
Published: over 5 years ago

10.3390/jcm9113517

Non-Invasive Prenatal Diagnosis of Retinoblastoma Inheritance by Combined Targeted Sequencing Strategies
Cited by: 6
Author(s): Amy Gerrish, Benjamin Bowns, Chipo Mashayamombe-Wolfgarten, Elizabeth Young, Samantha Court, Joshua Bott, Maureen McCalla, Simon Ramsden, Michael J. Parks, David Goudie, Sue Carless, Samuel Clokie, Trevor Cole, Stephanie Allen
Software Mentions: 2
Published: about 4 years ago

10.1186/s12881-017-0385-8

Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathy
Cited by: 7
Author(s): Matthew N. Bainbridge, Lili Li, Yanli Tan, Benjamin Cheong, Ali J. Marian
Software Mentions: 2
Published: over 7 years ago

10.1186/s12859-020-03704-1

Evaluation of variant calling tools for large plant genome re-sequencing
Cited by: 21
Author(s): Zhen Yao, Frank M. You, Amidou N’Diaye, Ron Knox, Curt A. McCartney, Colin W. Hiebert, Curtis Pozniak, Wayne Xu
Software Mentions: 2
Published: over 4 years ago

10.1371/journal.ppat.1007722

Covalent Plasmodium falciparum-selective proteasome inhibitors exhibit a low propensity for generating resistance in vitro and synergize with multiple antimalarial agents
Cited by: 52
Author(s): Barbara H. Stokes, Euna Yoo, James M. Murithi, Madeline R. Luth, Pavel Afanasyev, Paula C. A. da Fonseca, Elizabeth A. Winzeler, Caroline L. Ng, Matthew Bogyo, David A. Fidock
Software Mentions: 2
Published: over 5 years ago

10.1136/jmedgenet-2016-104215

Diagnostic value of exome and whole genome sequencing in craniosynostosis
Cited by: 92
Author(s): Kerry A. Miller, Stephen R.F. Twigg, Simon J. McGowan, Julie Phipps, Aimée L. Fenwick, David Johnson, Steven A. Wall, Peter Noons, Katie E. M. Rees, Elizabeth A Tidey, Judith Craft, John M. Taylor, Jenny C Taylor, Jacqueline A.C. Goos, Sigrid Swagemakers, Irene M J Mathijssen, Peter J. van der Spek, Helen Lord, Tracy Lester, Noina Abid, Deirdre Cilliers, Jane A. Hurst, Jenny Morton, Elizabeth Sweeney, Astrid Weber, Louise Wilson, Andrew O.M. Wilkie
Software Mentions: 2
Published: almost 8 years ago

10.1186/s12864-018-4734-6

Whole genome sequencing data of 1110 Mycobacterium tuberculosis isolates identifies insertions and deletions associated with drug resistance
Cited by: 12
Author(s): Xi Zeng, Jamie Sui-Lam Kwok, Kevin Yi Yang, Kenneth Leung, Mai Shi, Zhiyuan Yang, Wing-Cheong Yam, Stephen Kwok‐Wing Tsui
Software Mentions: 2
Published: over 6 years ago

10.1038/srep27806

Comparative chemical genomics reveal that the spiroindolone antimalarial KAE609 (Cipargamin) is a P-type ATPase inhibitor
Cited by: 36
Author(s): Gregory M. Goldgof, Jacob D. Durrant, Sabine Ottilie, Edgar Vigil, Kenneth E. Allen, Felicia Gunawan, Maxim Kostylev, Kiersten A. Henderson, Jennifer H. Yang, Jake Schenken, Gregory LaMonte, Mark J. Manary, Ayako Murao, Marie Nachon, Rebecca Stanhope, Maximo Prescott, Case W. McNamara, Carolyn W. Slayman, Rommie E. Amaro, Yo Suzuki, Elizabeth A. Winzeler
Software Mentions: 2
Published: over 8 years ago

10.1371/journal.pone.0136790

Genetic Adaptation of Achromobacter sp. during Persistence in the Lungs of Cystic Fibrosis Patients
Cited by: 41
Author(s): Winnie Ridderberg, Signe Maria Nielsen, Niels Nørskov‐Lauritsen
Software Mentions: 2
Published: about 9 years ago

10.1371/journal.pone.0181556

Novel and ultra-rare damaging variants in neuropeptide signaling are associated with disordered eating behaviors
Cited by: 38
Author(s): Michael Lutter, Ethan Bahl, Claire Hannah, Dabney Hofammann, Summer F. Acevedo, Huxing Cui, Carrie J. McAdams, Jacob J. Michaelson
Software Mentions: 2
Published: about 7 years ago

10.1371/journal.pone.0178169

Whole-genome sequencing of spermatocytic tumors provides insights into the mutational processes operating in the male germline
Cited by: 32
Author(s): Eleni Giannoulatou, Geoffrey J. Maher, Zhihao Ding, Gillis Ajm., Dorssers Lcj., Alexander Hoischen, Ewa Rajpert‐De Meyts, Gil McVean, Andrew O.M. Wilkie, Leendert H. J. Looijenga, Anne Goriely
Software Mentions: 2
Published: over 7 years ago

10.1371/journal.pone.0139851

Implementation of a Pan-Genomic Approach to Investigate Holobiont-Infecting Microbe Interaction: A Case Report of a Leukemic Patient with Invasive Mucormycosis
Cited by: 45
Author(s): Samuel A. Shelburne, Nadim J. Ajami, Marcus C. Chibucos, Hannah C. Beird, Jeffrey J. Tarrand, Jessica Galloway-Peña, Nathan D. Albert, Roy F. Chemaly, Shashank S. Ghantoji, Lisa Marsh, Naveen Pemmaraju, Michael Andreeff, Elizabeth J. Shpall, Jennifer A. Wargo, Katayoun Rezvani, Amin M. Alousi, Vincent M. Bruno, P. Andrew Futreal, Joseph F. Petrosino, Dimitrios P. Kontoyiannis
Software Mentions: 2
Published: about 9 years ago

10.7554/eLife.55207

A highly accurate platform for clone-specific mutation discovery enables the study of active mutational processes
Cited by: 4
Author(s): Mohammad KaramiNejadRanjbar, Sahand Sharifzadeh, Nina Wietek, Mara Artibani, Salma El-Sahhar, Tatjana Sauka‐Spengler, Christopher Yau, Volker Tresp, Ahmed A. Ahmed
Software Mentions: 2
Published: over 4 years ago

10.1371/journal.pone.0185103

Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders
Cited by: 18
Author(s): Dolores González‐Morón, Sebastián Vishnopolska, D. Consalvo, Nancy Medina, Marcelo A. Martí, Manuel Benabent Fernández de Córdoba, Cecilia Vazquez-Dusefante, Santiago Claverie, Sergio Alejandro Rodríguez-Quiroga, Patricia Vega, Walter Silva, Silvia Kochen, Marcelo Kauffman
Software Mentions: 2
Published: about 7 years ago

10.1038/srep43169

Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data
Cited by: 167
Author(s): Sarah Sandmann, Aniek O. de Graaf, Mohsen Karimi, Bert A. van der Reijden, Eva Hellström‐Lindberg, Joop H. Jansen, Martin Dugas
Software Mentions: 2
Published: over 7 years ago

10.1371/journal.pgen.0030002

Early History of Mammals Is Elucidated with the ENCODE Multiple Species Sequencing Data
Cited by: 105
Author(s): Sergey I. Nikolaev, Juan I. Montoya‐Burgos, Elliott H. Margulies, Nisc Comparative Sequencing Program, Jacques Rougemont, Bruno Nyffeler, Stylianos E. Antonarakis
Software Mentions: 2
Published: almost 18 years ago

10.1186/s12864-015-2059-2

Comparison among three variant callers and assessment of the accuracy of imputation from SNP array data to whole-genome sequence level in chicken
Cited by: 19
Author(s): Guiyan Ni, Tim M. Strom, Hubert Pausch, Christian Reimer, Rudolf Preisinger, Henner Simianer, Malena Erbe
Software Mentions: 2
Published: about 9 years ago

10.3390/cancers11040545

Identification of KIF11 As a Novel Target in Meningioma
Cited by: 27
Author(s): Gerhard Jungwirth, Yu Tao, Mahmoud Moustafa, Carmen Rapp, Rolf Warta, Christine Jungk, Felix Sahm, Steffen Dettling, Klaus Zweckberger, Katrin Lamszus, Christian Senft, Mario Loehr, Almuth F. Keßler, Ralf Ketter, Manfred Westphal, J. Debus, Andreas von Deimling, Matthias Simon, Andreas Unterberg, Amir Abdollahi, Christel Herold‐Mende
Software Mentions: 2
Published: over 5 years ago

10.3390/cancers12082231

Utility of Circulating Tumor DNA for Detection and Monitoring of Endometrial Cancer Recurrence and Progression
Cited by: 30
Author(s): Esther L Moss, Diviya N. Gorsia, Anna Collins, Pavandeep Sandhu, Nalini Foreman, A. Jesse Gore, Joey Wood, Christopher Kent, Lee Silcock, David S. Guttery
Software Mentions: 2
Published: over 4 years ago

10.3390/cancers12061441

A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer
Cited by: 20
Author(s): Aayushi Srivastava, Benchun Miao, Diamanto Skopelitou, Vaijayanti A. Kumar, Abhishek Kumar, Nagarajan Paramasivam, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
Software Mentions: 2
Published: over 4 years ago

10.3390/cancers12040986

Identifying Genetic Lesions in Ocular Adnexal Extranodal Marginal Zone Lymphomas of the MALT Subtype by Whole Genome, Whole Exome and Targeted Sequencing
Cited by: 16
Author(s): Patricia Johansson, Ludger Klein-Hitpaß, Bettina Budeus, Matthias Kühn, Chris Lauber, Michael Seifert, Ingo Roeder, Roman Pförtner, Martin Stuschke, Ulrich Dührsen, Anja Eckstein, Jan Dürig, Ralf Küppers
Software Mentions: 2
Published: over 4 years ago

10.3390/cancers12102770

Cancer Predisposition Genes in Cancer-Free Families
Cited by: 1
Author(s): Guoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, Nagarajan Paramasivam, Subhayan Chattopadhyay, Matthias Schlesner, Rolf H. Sijmons, Akseli Hemminki, Dagmara Dymerska, Jan Lubiński, Kari Hemminki, Asta Försti
Software Mentions: 2
Published: about 4 years ago

10.3390/ijms20133364

Integrated Approach Reveals Role of Mitochondrial Germ-Line Mutation F18L in Respiratory Chain, Oxidative Alterations, Drug Sensitivity, and Patient Prognosis in Glioblastoma
Cited by: 9
Author(s): Kathleen Keatley, Samuel Stromei-Cleroux, Tammy Wiltshire, Nina Rajala, Gary V. Burton, William V. Holt, D. Timothy J. Littlewood, Andrew G. Briscoe, Josephine Jung, Keyoumars Ashkan, Simon Heales, Geoffrey J. Pilkington, Brigitte Meunier, J.E. McGeehan, Iain P. Hargreaves, Rhiannon E. McGeehan
Software Mentions: 2
Published: over 5 years ago

10.1186/s12902-020-0493-x

Case report: recurrent pituitary adenoma has increased load of somatic variants
Cited by: 2
Author(s): Raitis Pečulis, Inga Balcere, Ilze Radoviča-Spalviņa, Ilze Konrāde, Olivija Caune, Kaspars Megnis, Vita Rovīte, Jānis Stukēns, Jurijs Nazarovs, Austra Breikša, Aigars Kiecis, Ivars Silamiķelis, Valdis Pīrāgs, Jānis Kloviņš
Software Mentions: 2
Published: almost 5 years ago

10.1016/j.celrep.2016.04.090

De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation
Cited by: 27
Author(s): Matilda Haas, Linh Ngo, Shan Shan Li, Sibylle Schleich, Zhengdong Qu, Hannah K. Vanyai, Hayley Daniella Cullen, Aida Cardona-Alberich, Ivan Gladwyn-Ng, Alistair T. Pagnamenta, Jenny C. Taylor, Helen Stewart, Usha Kini, Kent E. Duncan, Aurelio A. Teleman, David A. Keays, Julian Ik‐Tsen Heng
Software Mentions: 2
Published: over 8 years ago

10.1371/journal.pgen.1003074

Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development
Cited by: 92
Author(s): Stefano Lise, Yvonne L. Clarkson, Emma M. Perkins, Alexandra Kwasniewska, Elham Sadighi Akha, Ricardo Parolin Schnekenberg, Daumante Šuminaite, Jilly Hope, Ian Baker, Lorna Gregory, Angie Green, Chris Allan, Sarah Lamble, Sandeep Jayawant, Gerardine Quaghebeur, M Z Cader, Sarah M. Hughes, Richard J. E. Armstrong, Alexander Kanapin, Andrew Rimmer, Gerton Lunter, Iain Mathieson, Jean‐Baptiste Cazier, David Buck, Jenny C. Taylor, David Bentley, Gil McVean, Peter Donnelly, Samantha J. L. Knight, Mandy Jackson, Jiannis Ragoussis, Andrea H. Németh
Software Mentions: 2
Published: almost 12 years ago

10.1161/CIRCGENETICS.116.001431

Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction
Cited by: 62
Author(s): Robert K. Hastings, Carin Pamela de Villiers, Charlotte Hooper, Liz Ormondroyd, Alistair T. Pagnamenta, Stefano Lise, Silvia Salatino, Samantha J. L. Knight, Jenny C. Taylor, Kate Thomson, Linda Arnold, Spyros D. Chatziefthimiou, Petr V. Konarev, Matthias Wilmanns, Elisabeth Ehler, Andrea Ghisleni, Mathias Gautel, Edward Blair, Hugh Watkins, Katja Gehmlich
Software Mentions: 2
Published: about 8 years ago

10.1098/rstb.2020.0089

A 180 Myr-old female-specific genome region in sturgeon reveals the oldest known vertebrate sex determining system with undifferentiated sex chromosomes
Cited by: 32
Author(s): Heiner Kuhl, Yann Guiguen, Christin Höhne, Eva Kreuz, Kang Du, Christophe Klopp, Céline Roques, Elena Santidrián Yebra-Pimentel, Mitică Ciorpac, Jörn Geßner, Daniela Holostenco, Wibke Kleiner, Klaus Kohlmann, Dunja K. Lamatsch, Dmitry Prokopov, Anastasia Bestin, Emmanuel Bonpunt, Bastien Debeuf, Pierrick Haffray, Romain Morvezen, Pierre Patrice, Radu Suciu, Ron P. Dirks, Sven Wuertz, Werner Kloas, Manfred Schartl, Matthias Stöck
Software Mentions: 2
Published: over 3 years ago