A citation-based method for searching scientific literature

Jordan G Nestor, Emily E Groopman, Ali G Gharavi. J Nephrol 2018
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Jing Chen, Asaf Vivante, Daw-Yang Hwang, Julian Schulz, Daniela A Braun,[...]. J Am Soc Nephrol 2018
55
33

Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.
Mir Reza Bekheirnia, Nasim Bekheirnia, Matthew N Bainbridge, Shen Gu, Zeynep Hande Coban Akdemir, Tomek Gambin, Nicolette K Janzen, Shalini N Jhangiani, Donna M Muzny, Mini Michael,[...]. Genet Med 2017
42
33

Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.
Agnieszka Bierzynska, Hugh J McCarthy, Katrina Soderquest, Ethan S Sen, Elizabeth Colby, Wen Y Ding, Marwa M Nabhan, Larissa Kerecuk, Shivram Hegde, David Hughes,[...]. Kidney Int 2017
97
33

Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
Sneh Lata, Maddalena Marasa, Yifu Li, David A Fasel, Emily Groopman, Vaidehi Jobanputra, Hila Rasouly, Adele Mitrotti, Rik Westland, Miguel Verbitsky,[...]. Ann Intern Med 2018
72
33

APOL1 risk variants, race, and progression of chronic kidney disease.
Afshin Parsa, W H Linda Kao, Dawei Xie, Brad C Astor, Man Li, Chi-yuan Hsu, Harold I Feldman, Rulan S Parekh, John W Kusek, Tom H Greene,[...]. N Engl J Med 2013
445
33

Technique to Target Microinjection to the Developing Xenopus Kidney.
Bridget D DeLay, Vanja Krneta-Stankic, Rachel K Miller. J Vis Exp 2016
9
16

Development of the Xenopus pronephric system.
P D Vize, E A Jones, R Pfister. Dev Biol 1995
114
16

Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.
B W M van Bon, B P Coe, R Bernier, C Green, J Gerdts, K Witherspoon, T Kleefstra, M H Willemsen, R Kumar, P Bosco,[...]. Mol Psychiatry 2016
82
16

Isolation of DNA from red blood cells in Xenopus.
Hazel L Sive, Robert M Grainger, Richard M Harland. Cold Spring Harb Protoc 2012
1
100

The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy.
Jean-Benoît Courcet, Laurence Faivre, Perrine Malzac, Alice Masurel-Paulet, Estelle Lopez, Patrick Callier, Laetitia Lambert, Martine Lemesle, Julien Thevenon, Nadège Gigot,[...]. J Med Genet 2012
61
16

Activation-loop autophosphorylation is mediated by a novel transitional intermediate form of DYRKs.
Pamela A Lochhead, Gary Sibbet, Nick Morrice, Vaughn Cleghon. Cell 2005
195
16

Down's-syndrome-related kinase Dyrk1A modulates the p120-catenin-Kaiso trajectory of the Wnt signaling pathway.
Ji Yeon Hong, Jae-Il Park, Moonsup Lee, William A Muñoz, Rachel K Miller, Hong Ji, Dongmin Gu, Jerome Ezan, Sergei Y Sokol, Pierre D McCrea. J Cell Sci 2012
30
16

Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome.
Juan Arranz, Elisa Balducci, Krisztina Arató, Gentzane Sánchez-Elexpuru, Sònia Najas, Alberto Parras, Elena Rebollo, Isabel Pijuan, Ionas Erb, Gaetano Verde,[...]. Neurobiol Dis 2019
11
16

Mutations in DSTYK and dominant urinary tract malformations.
Simone Sanna-Cherchi, Rosemary V Sampogna, Natalia Papeta, Katelyn E Burgess, Shannon N Nees, Brittany J Perry, Murim Choi, Monica Bodria, Yan Liu, Patricia L Weng,[...]. N Engl J Med 2013
71
16

DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies.
Jianling Ji, Hane Lee, Bob Argiropoulos, Naghmeh Dorrani, John Mann, Julian A Martinez-Agosto, Natalia Gomez-Ospina, Natalie Gallant, Jonathan A Bernstein, Louanne Hudgins,[...]. Eur J Hum Genet 2015
54
16

Functional characterization of DYRK1A missense variants associated with a syndromic form of intellectual deficiency and autism.
Esti Wahyu Widowati, Sabrina Ernst, Ralf Hausmann, Gerhard Müller-Newen, Walter Becker. Biol Open 2018
11
16

Distinct and sequential tissue-specific activities of the LIM-class homeobox gene Lim1 for tubular morphogenesis during kidney development.
Akio Kobayashi, Kin-Ming Kwan, Thomas J Carroll, Andrew P McMahon, Cathy L Mendelsohn, Richard R Behringer. Development 2005
237
16


Modeling congenital kidney diseases in Xenopus laevis.
Alexandria T M Blackburn, Rachel K Miller. Dis Model Mech 2019
6
16

Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders.
Jochem M G Evers, Roman A Laskowski, Marta Bertolli, Jill Clayton-Smith, Charu Deshpande, Jacqueline Eason, Frances Elmslie, Frances Flinter, Carol Gardiner, Jane A Hurst,[...]. Hum Mol Genet 2017
18
16

TNXB mutations can cause vesicoureteral reflux.
Rasheed A Gbadegesin, Patrick D Brophy, Adebowale Adeyemo, Gentzon Hall, Indra R Gupta, David Hains, Bartlomeij Bartkowiak, C Egla Rabinovich, Settara Chandrasekharappa, Alison Homstad,[...]. J Am Soc Nephrol 2013
43
16


Dynamin Binding Protein Is Required for Xenopus laevis Kidney Development.
Bridget D DeLay, Tanya A Baldwin, Rachel K Miller. Front Physiol 2019
6
16


Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy.
James R Lupski, Claudia Gonzaga-Jauregui, Yaping Yang, Matthew N Bainbridge, Shalini Jhangiani, Christian J Buhay, Christie L Kovar, Min Wang, Alicia C Hawes, Jeffrey G Reid,[...]. Genome Med 2013
113
16



Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.
Rikke S Møller, Sabine Kübart, Maria Hoeltzenbein, Babett Heye, Ida Vogel, Christian P Hansen, Corinna Menzel, Reinhard Ullmann, Niels Tommerup, Hans-Hilger Ropers,[...]. Am J Hum Genet 2008
110
16

Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations.
Rajshekhar Chatterjee, Enrique Ramos, Mary Hoffman, Jessica VanWinkle, Daniel R Martin, Thomas K Davis, Masato Hoshi, Stanley P Hmiel, Anne Beck, Keith Hruska,[...]. Hum Genet 2012
52
16

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
16

Renal progenitors: an evolutionary conserved strategy for kidney regeneration.
Paola Romagnani, Laura Lasagni, Giuseppe Remuzzi. Nat Rev Nephrol 2013
113
16

Evolutionary trend for metamery reduction and gonad shortening in Anurans revealed by comparison of gonad development.
Rafal P Piprek, Anna Pecio, Malgorzata Kloc, Jacek Z Kubiak, Jacek M Szymura. Int J Dev Biol 2014
6
16

Integrin alpha5beta1 and fibronectin regulate polarized cell protrusions required for Xenopus convergence and extension.
Lance A Davidson, Mungo Marsden, Raymond Keller, Douglas W Desimone. Curr Biol 2006
140
16


Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
16

Organization of the pronephric kidney revealed by large-scale gene expression mapping.
Daniela Raciti, Luca Reggiani, Lars Geffers, Qiuhong Jiang, Francesca Bacchion, Astrid E Subrizi, Dave Clements, Christopher Tindal, Duncan R Davidson, Brigitte Kaissling,[...]. Genome Biol 2008
80
16

Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling.
Ryan D Morin, Elbert Chang, Anca Petrescu, Nancy Liao, Malachi Griffith, William Chow, Robert Kirkpatrick, Yaron S Butterfield, Alice C Young, Jeffrey Stott,[...]. Genome Res 2006
59
16

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.
Matthew N Bainbridge, Min Wang, Yuanqing Wu, Irene Newsham, Donna M Muzny, John L Jefferies, Thomas J Albert, Daniel L Burgess, Richard A Gibbs. Genome Biol 2011
144
16


Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome.
Ashish K Solanki, Eugen Widmeier, Ehtesham Arif, Shailza Sharma, Ankana Daga, Pankaj Srivastava, Sang-Ho Kwon, Hannah Hugo, Makiko Nakayama, Nina Mann,[...]. Kidney Int 2019
8
16

Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases.
Diana Chang, Feng Gao, Andrea Slavney, Li Ma, Yedael Y Waldman, Aaron J Sams, Paul Billing-Ross, Aviv Madar, Richard Spritz, Alon Keinan. PLoS One 2014
63
16

Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.
Rainer G Ruf, Arno Fuchshuber, Stephanie M Karle, Arnaud Lemainque, Kirsten Huck, Thomas Wienker, Edgar Otto, Friedhelm Hildebrandt. J Am Soc Nephrol 2003
24
16

Weighted gene co‑expression network analysis for identifying hub genes in association with prognosis in Wilms tumor.
Xiaofu Wang, Pan Song, Chuiguo Huang, Naijun Yuan, Xinghua Zhao, Changbao Xu. Mol Med Rep 2019
9
16

Anti-centromere antibody is an independent risk factor for chronic kidney disease in patients with primary biliary cirrhosis.
Shintaro Mandai, Eiichiro Kanda, Yohei Arai, Suguru Hirasawa, Toshiyuki Hirai, Shota Aki, Naoto Inaba, Makoto Aoyagi, Hiroyuki Tanaka, Takaaki Ikeda,[...]. Clin Exp Nephrol 2013
5
20

Regulation of spindle and kinetochore-associated protein 1 by antitumor miR-10a-5p in renal cell carcinoma.
Takayuki Arai, Atsushi Okato, Satoko Kojima, Tetsuya Idichi, Keiichi Koshizuka, Akira Kurozumi, Mayuko Kato, Kazuto Yamazaki, Yasuo Ishida, Yukio Naya,[...]. Cancer Sci 2017
31
16

Sequence analysis of four vitamin D family genes (VDR, CYP24A1, CYP27B1 and CYP2R1) in Vogt-Koyanagi-Harada (VKH) patients: identification of a potentially pathogenic variant in CYP2R1.
Ma'an Abdullah Al-Barry, Alia M Albalawi, Mohammed Abu Sayf, Abdulrahman Badawi, Sibtain Afzal, Muhammad Latif, Mohammed I Samman, Sulman Basit. BMC Ophthalmol 2016
6
16

Contributions of the Transplant Registry: The 2006 Annual Report of the North American Pediatric Renal Trials and Collaborative Studies (NAPRTCS).
Jodi M Smith, Donald M Stablein, Ricardo Munoz, Diane Hebert, Ruth A McDonald. Pediatr Transplant 2007
158
16

Antinuclear antibodies and clinical associations in a british cohort with limited cutaneous systemic sclerosis.
Angela E Gliddon, Caroline J Doré, Juliet Dunphy, Zoë Betteridge, Neil J McHugh, Peter J Maddison. J Rheumatol 2011
10
16




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.