A citation-based method for searching scientific literature

Moran Hausman-Kedem, Liat Ben-Sira, Debora Kidron, Shay Ben-Shachar, Rachel Straussberg, Daphna Marom, Penina Ponger, Anat Bar-Shira, Gustavo Malinger, Aviva Fattal-Valevski. Eur J Hum Genet 2021
Times Cited: 2







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


A comparison of genotyping arrays.
Joost A M Verlouw, Eva Clemens, Jard H de Vries, Oliver Zolk, Annemieke J M H Verkerk, Antoinette Am Zehnhoff-Dinnesen, Carolina Medina-Gomez, Claudia Lanvers-Kaminsky, Fernando Rivadeneira, Thorsten Langer,[...]. Eur J Hum Genet 2021
5
50

Stakeholders' views of integrating universal tumour screening and genetic testing for colorectal and endometrial cancer into routine oncology.
Rosie O'Shea, Nicole M Rankin, Maira Kentwell, Margaret Gleeson, Katherine M Tucker, Heather Hampel, Natalie Taylor, Sarah Lewis. Eur J Hum Genet 2021
1
100

A systematic review assessing the existence of pneumothorax-only variants of FLCN. Implications for lifelong surveillance of renal tumours.
Kenki Matsumoto, Derek Lim, Paul D Pharoah, Eamonn R Maher, Stefan J Marciniak. Eur J Hum Genet 2021
3
50

TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility.
Aafke Engwerda, Erika K S M Leenders, Barbara Frentz, Paulien A Terhal, Katharina Löhner, Bert B A de Vries, Trijnie Dijkhuizen, Yvonne J Vos, Tuula Rinne, Maarten P van den Berg,[...]. Eur J Hum Genet 2021
5
50

The genetic structure of Norway.
Morten Mattingsdal, S Sunna Ebenesersdóttir, Kristjan H S Moore, Ole A Andreassen, Thomas F Hansen, Thomas Werge, Ingrid Kockum, Tomas Olsson, Lars Alfredsson, Agnar Helgason,[...]. Eur J Hum Genet 2021
3
50

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect.
Alisdair McNeill, Emanuela Iovino, Luke Mansard, Christel Vache, David Baux, Emma Bedoukian, Helen Cox, John Dean, David Goudie, Ajith Kumar,[...]. Brain 2020
16
50

Identifying challenges in neurofibromatosis: a modified Delphi procedure.
Britt A E Dhaenens, Rosalie E Ferner, Annette Bakker, Marco Nievo, D Gareth Evans, Pierre Wolkenstein, Cornelia Potratz, Scott R Plotkin, Guenter Heimann, Eric Legius,[...]. Eur J Hum Genet 2021
1
100

Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability.
Natja Haag, Ene-Choo Tan, Matthias Begemann, Lars Buschmann, Florian Kraft, Petra Holschbach, Angeline H M Lai, Maggie Brett, Ganeshwaran H Mochida, Stephanie DiTroia,[...]. Eur J Hum Genet 2021
3
50

clusterProfiler: an R package for comparing biological themes among gene clusters.
Guangchuang Yu, Li-Gen Wang, Yanyan Han, Qing-Yu He. OMICS 2012
50


ER stress and the unfolded protein response.
Martin Schröder, Randal J Kaufman. Mutat Res 2005
50

Ophthalmological features associated with COL4A1 mutations.
Isabelle Coupry, Igor Sibon, Bruno Mortemousque, François Rouanet, Manuele Mine, Cyril Goizet. Arch Ophthalmol 2010
40
50

Identification of fibronectin 1 as a candidate genetic modifier in a Col4a1 mutant mouse model of Gould syndrome.
Mao Mao, Tanav Popli, Marion Jeanne, Kendall Hoff, Saunak Sen, Douglas B Gould. Dis Model Mech 2021
3
50


4-Sodium phenyl butyric acid has both efficacy and counter-indicative effects in the treatment of Col4a1 disease.
Frances E Jones, Lydia S Murray, Sarah McNeilly, Afshan Dean, Alisha Aman, Yinhui Lu, Nija Nikolova, Ruben Malomgré, Karen Horsburgh, William M Holmes,[...]. Hum Mol Genet 2019
13
50

Beyond the Brain: Systematic Review of Extracerebral Phenotypes Associated With Monogenic Cerebral Small Vessel Disease.
Kristiina Rannikmäe, David E Henshall, Sophie Thrippleton, Qiu Ginj Kong, Mike Chong, Nickrooz Grami, Isaac Kuan, Tim Wilkinson, Blair Wilson, Kirsty Wilson,[...]. Stroke 2020
7
50

COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic Heterogeneity.
Cassandre Labelle-Dumais, Vera Schuitema, Genki Hayashi, Kendall Hoff, Wenhui Gong, Dang Q Dao, Erik M Ullian, Peter Oishi, Marta Margeta, Douglas B Gould. Am J Hum Genet 2019
20
50

Assembly of lamina-specific neuronal connections by slit bound to type IV collagen.
Tong Xiao, Wendy Staub, Estuardo Robles, Nathan J Gosse, Gregory J Cole, Herwig Baier. Cell 2011
75
50

Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells.
Lars M Ittner, Heiko Wurdak, Kerstin Schwerdtfeger, Thomas Kunz, Fabian Ille, Per Leveen, Tord A Hjalt, Ueli Suter, Stefan Karlsson, Farhad Hafezi,[...]. J Biol 2005
91
50

foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish.
Thomas R Whitesell, Paul W Chrystal, Jae-Ryeon Ryu, Nicole Munsie, Ann Grosse, Curtis R French, Matthew L Workentine, Rui Li, Lihua Julie Zhu, Andrew Waskiewicz,[...]. Dev Biol 2019
22
50

Angiotensin II type 2 receptor signaling attenuates aortic aneurysm in mice through ERK antagonism.
Jennifer P Habashi, Jefferson J Doyle, Tammy M Holm, Hamza Aziz, Florian Schoenhoff, Djahida Bedja, YiChun Chen, Alexandra N Modiri, Daniel P Judge, Harry C Dietz. Science 2011
305
50

Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome mice.
Tammy M Holm, Jennifer P Habashi, Jefferson J Doyle, Djahida Bedja, YiChun Chen, Christel van Erp, Mark E Lindsay, David Kim, Florian Schoenhoff, Ronald D Cohn,[...]. Science 2011
331
50

WikiPathways: connecting communities.
Marvin Martens, Ammar Ammar, Anders Riutta, Andra Waagmeester, Denise N Slenter, Kristina Hanspers, Ryan A Miller, Daniela Digles, Elisson N Lopes, Friederike Ehrhart,[...]. Nucleic Acids Res 2021
117
50

Iris Malformation and Anterior Segment Dysgenesis in Mice and Humans With a Mutation in PI 3-Kinase.
Marie H Solheim, Allen C Clermont, Jonathon N Winnay, Erlend Hallstensen, Anders Molven, Pål R Njølstad, Eyvind Rødahl, C Ronald Kahn. Invest Ophthalmol Vis Sci 2017
7
50

COL4A1-related autosomal recessive encephalopathy in 2 Turkish children.
Ahmet Yaramis, Hanns Lochmüller, Ana Töpf, Ece Sonmezler, Elmasnur Yilmaz, Semra Hiz, Uluc Yis, Serdal Gungor, Ayse Ipek Polat, Pinar Edem,[...]. Neurol Genet 2020
4
50

Transforming growth factor beta 1 null mutation in mice causes excessive inflammatory response and early death.
A B Kulkarni, C G Huh, D Becker, A Geiser, M Lyght, K C Flanders, A B Roberts, M B Sporn, J M Ward, S Karlsson. Proc Natl Acad Sci U S A 1993
50

Integrin β1 is necessary for the maintenance of corneal structural integrity.
Sunil K Parapuram, Kun Huh, Shangxi Liu, Andrew Leask. Invest Ophthalmol Vis Sci 2011
16
50

A second report of recessive type COL4A1-related disorder: a novel homozygous missense variant.
Ataf H Sabir, Ananya Singh, George Elley, Evangeline Wassemer, Katharine Foster, Melissa Sloman, Derek Lim. Clin Dysmorphol 2021
1
100

Integrin alpha 2 beta 1 mediates interactions between developing embryonic retinal cells and collagen.
A D Bradshaw, K M McNagny, D B Gervin, G M Cann, T Graf, D O Clegg. Development 1995
58
50

COL4A1 mutations in two infants with congenital cataracts and porencephaly: an ophthalmologic perspective.
Shane Nau, Emily A McCourt, John A Maloney, Johan L Van Hove, Margarita Saenz, Jennifer L Jung. J AAPOS 2019
4
50

Recessive COL4A2 Mutation Leads to Intellectual Disability, Epilepsy, and Spastic Cerebral Palsy.
Somayeh Bakhtiari, Abbas Tafakhori, Sheng Chih Jin, Brandon S Guida, Elham Alehabib, Saghar Firouzbadi, Kaya Bilguvar, Michael C Fahey, Hossein Darvish, Michael C Kruer. Neurol Genet 2021
2
50


3D map of the human corneal endothelial cell.
Zhiguo He, Fabien Forest, Philippe Gain, Damien Rageade, Aurélien Bernard, Sophie Acquart, Michel Peoc'h, Dennis M Defoe, Gilles Thuret. Sci Rep 2016
39
50

COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes.
Liina Kuuluvainen, Saana Mönkäre, Hannaleena Kokkonen, Fang Zhao, Auli Verkkoniemi-Ahola, Johanna Schleutker, Anna H Hakonen, Päivi Hartikainen, Minna Pöyhönen, Liisa Myllykangas. Stroke 2021
1
100


Developmental distribution of collagen IV isoforms and relevance to ocular diseases.
Xiaoyang Bai, David J Dilworth, Yi-Chinn Weng, Douglas B Gould. Matrix Biol 2009
33
50

Type IV collagens regulate BMP signalling in Drosophila.
Xiaomeng Wang, Robin E Harris, Laura J Bayston, Hilary L Ashe. Nature 2008
228
50

p38 MAP kinase inhibitor suppresses transforming growth factor-β2-induced type 1 collagen production in trabecular meshwork cells.
Miyuki Inoue-Mochita, Toshihiro Inoue, Tomokazu Fujimoto, Takanori Kameda, Nanako Awai-Kasaoka, Naoki Ohtsu, Kenichi Kimoto, Hidenobu Tanihara. PLoS One 2015
18
50

TGFbeta2 knockout mice have multiple developmental defects that are non-overlapping with other TGFbeta knockout phenotypes.
L P Sanford, I Ormsby, A C Gittenberger-de Groot, H Sariola, R Friedman, G P Boivin, E L Cardell, T Doetschman. Development 1997
50


WebGestalt 2019: gene set analysis toolkit with revamped UIs and APIs.
Yuxing Liao, Jing Wang, Eric J Jaehnig, Zhiao Shi, Bing Zhang. Nucleic Acids Res 2019
838
50

PITX2 is involved in stress response in cultured human trabecular meshwork cells through regulation of SLC13A3.
M Hermina Strungaru, Tim Footz, Yi Liu, Fred B Berry, Pascal Belleau, Elena V Semina, Vincent Raymond, Michael A Walter. Invest Ophthalmol Vis Sci 2011
24
50

Cerebral small-vessel disease associated with COL4A1 and COL4A2 gene duplications.
Dimitri Renard, Manuele Miné, Eva Pipiras, Pierre Labauge, Andrée Delahaye, Brigitte Benzacken, Elisabeth Tournier-Lasserve. Neurology 2014
15
50

Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations.
Barbara D'haene, Françoise Meire, Ilse Claerhout, Hester Y Kroes, Astrid Plomp, Yvonne H Arens, Thomy de Ravel, Ingele Casteels, Sarah De Jaegere, Sally Hooghe,[...]. Invest Ophthalmol Vis Sci 2011
55
50


Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting protein.
Moulinath Acharya, Michael W Sharp, Farideh Mirzayans, Tim Footz, Lijia Huang, Chanchal Birdi, Michael A Walter. Mol Vis 2012
4
50

Clinical pharmacokinetics of losartan.
Domenic A Sica, Todd W B Gehr, Siddhartha Ghosh. Clin Pharmacokinet 2005
117
50


Type IV collagen is an activating ligand for the adhesion G protein-coupled receptor GPR126.
Kevin J Paavola, Harwin Sidik, J Bradley Zuchero, Michael Eckart, William S Talbot. Sci Signal 2014
113
50

The activin receptor is stimulated in the skeleton, vasculature, heart, and kidney during chronic kidney disease.
Matthew J Williams, Toshifumi Sugatani, Olga A Agapova, Yifu Fang, Joseph P Gaut, Marie-Claude Faugere, Hartmut H Malluche, Keith A Hruska. Kidney Int 2018
39
50


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.