A citation-based method for searching scientific literature

Asaf Vivante, Friedhelm Hildebrandt. Nat Rev Nephrol 2016
Times Cited: 134







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



Times Cited
  Times     Co-cited
Similarity


A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Carolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, Werner L Pabst, Heon Yung Gee, Stefan Kohl, Susanne Engelmann, Virginia Vega-Warner, Humphrey Fang, Jan Halbritter,[...]. J Am Soc Nephrol 2015
287
34

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
25

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Jillian K Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A Lawson, Shirlee Shril, Svjetlana Lovric, Shazia Ashraf, Jia Rao, Tobias Hermle,[...]. Clin J Am Soc Nephrol 2018
72
30

Genetic testing in steroid-resistant nephrotic syndrome: when and how?
Svjetlana Lovric, Shazia Ashraf, Weizhen Tan, Friedhelm Hildebrandt. Nephrol Dial Transplant 2016
104
21

Diagnostic Utility of Exome Sequencing for Kidney Disease.
Emily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, Slavé Petrovski, Vimla S Aggarwal, Hila Milo-Rasouly, Yifu Li, Junying Zhang, Jordan Nestor, Priya Krithivasan,[...]. N Engl J Med 2019
144
20

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
26

Genetic kidney diseases.
Friedhelm Hildebrandt. Lancet 2010
169
17

Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
46
36

Monogenic causes of chronic kidney disease in adults.
Dervla M Connaughton, Claire Kennedy, Shirlee Shril, Nina Mann, Susan L Murray, Patrick A Williams, Eoin Conlon, Makiko Nakayama, Amelie T van der Ven, Hadas Ityel,[...]. Kidney Int 2019
47
34

Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.
Christine Gast, Reuben J Pengelly, Matthew Lyon, David J Bunyan, Eleanor G Seaby, Nikki Graham, Gopalakrishnan Venkat-Raman, Sarah Ennis. Nephrol Dial Transplant 2016
100
15

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
15

Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
Agnes Trautmann, Monica Bodria, Fatih Ozaltin, Alaleh Gheisari, Anette Melk, Marta Azocar, Ali Anarat, Salim Caliskan, Francesco Emma, Jutta Gellermann,[...]. Clin J Am Soc Nephrol 2015
133
15

Rare inherited kidney diseases: challenges, opportunities, and perspectives.
Olivier Devuyst, Nine V A M Knoers, Giuseppe Remuzzi, Franz Schaefer. Lancet 2014
110
15

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
27

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
14

Guidelines for investigating causality of sequence variants in human disease.
D G MacArthur, T A Manolio, D P Dimmock, H L Rehm, J Shendure, G R Abecasis, D R Adams, R B Altman, S E Antonarakis, E A Ashley,[...]. Nature 2014
767
14

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.
Shazia Ashraf, Heon Yung Gee, Stephanie Woerner, Letian X Xie, Virginia Vega-Warner, Svjetlana Lovric, Humphrey Fang, Xuewen Song, Daniel C Cattran, Carmen Avila-Casado,[...]. J Clin Invest 2013
189
12

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
12

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
Saskia F Heeringa, Gil Chernin, Moumita Chaki, Weibin Zhou, Alexis J Sloan, Ziming Ji, Letian X Xie, Leonardo Salviati, Toby W Hurd, Virginia Vega-Warner,[...]. J Clin Invest 2011
234
11

Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity.
Daniela A Braun, Markus Schueler, Jan Halbritter, Heon Yung Gee, Jonathan D Porath, Jennifer A Lawson, Rannar Airik, Shirlee Shril, Susan J Allen, Deborah Stein,[...]. Kidney Int 2016
47
23

Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
Stefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, Alina C Hilger, Pawaree Saisawat, Asaf Vivante, Natasa Stajic, Radovan Bogdanovic, Heiko M Reutter, Elijah O Kehinde,[...]. J Am Soc Nephrol 2014
59
18

Copy-number disorders are a common cause of congenital kidney malformations.
Simone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, Monica Bodria, Matthew G Sampson, Dexter Hadley, Shannon N Nees, Miguel Verbitsky, Brittany J Perry, Roel Sterken,[...]. Am J Hum Genet 2012
122
11

Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.
Asaf Vivante, Daw-Yang Hwang, Stefan Kohl, Jing Chen, Shirlee Shril, Julian Schulz, Amelie van der Ven, Ghaleb Daouk, Neveen A Soliman, Aravind Selvin Kumar,[...]. J Am Soc Nephrol 2017
43
25

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Andrew F Malone, Paul J Phelan, Gentzon Hall, Umran Cetincelik, Alison Homstad, Andrea S Alonso, Ruiji Jiang, Thomas B Lindsey, Guanghong Wu, Matthew A Sparks,[...]. Kidney Int 2014
109
11

Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome.
Kálmán Tory, Dóra K Menyhárd, Stéphanie Woerner, Fabien Nevo, Olivier Gribouval, Andrea Kerti, Pál Stráner, Christelle Arrondel, Evelyne Huynh Cong, Tivadar Tulassay,[...]. Nat Genet 2014
84
11

From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline.
Geraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, Ryan Poplin, Guillermo Del Angel, Ami Levy-Moonshine, Tadeusz Jordan, Khalid Shakir, David Roazen, Joel Thibault,[...]. Curr Protoc Bioinformatics 2013
10

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
10

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.
Daw-Yang Hwang, Gabriel C Dworschak, Stefan Kohl, Pawaree Saisawat, Asaf Vivante, Alina C Hilger, Heiko M Reutter, Neveen A Soliman, Radovan Bogdanovic, Elijah O Kehinde,[...]. Kidney Int 2014
122
10

Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders.
Andrew J Mallett, Hugh J McCarthy, Gladys Ho, Katherine Holman, Elizabeth Farnsworth, Chirag Patel, Jeffery T Fletcher, Amali Mallawaarachchi, Catherine Quinlan, Bruce Bennetts,[...]. Kidney Int 2017
35
28

Epidemiology of chronic kidney disease in children.
Jérôme Harambat, Karlijn J van Stralen, Jon Jin Kim, E Jane Tizard. Pediatr Nephrol 2012
365
10

The Irish Kidney Gene Project--Prevalence of Family History in Patients with Kidney Disease in Ireland.
Dervla M Connaughton, Sarah Bukhari, Peter Conlon, Eoin Cassidy, Michael O'Toole, Mardina Mohamad, John Flanagan, Triona Butler, Anne O'Leary, Limy Wong,[...]. Nephron 2015
18
55

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
Nina Mann, Daniela A Braun, Kassaundra Amann, Weizhen Tan, Shirlee Shril, Dervla M Connaughton, Makiko Nakayama, Ronen Schneider, Thomas M Kitzler, Amelie T van der Ven,[...]. J Am Soc Nephrol 2019
35
28

Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome.
Daniela A Braun, Carolin E Sadowski, Stefan Kohl, Svjetlana Lovric, Susanne A Astrinidis, Werner L Pabst, Heon Yung Gee, Shazia Ashraf, Jennifer A Lawson, Shirlee Shril,[...]. Nat Genet 2016
80
11

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.
M Kestilä, U Lenkkeri, M Männikkö, J Lamerdin, P McCready, H Putaala, V Ruotsalainen, T Morita, M Nissinen, R Herva,[...]. Mol Cell 1998
9

Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies.
Heon Yung Gee, Edgar A Otto, Toby W Hurd, Shazia Ashraf, Moumita Chaki, Andrew Cluckey, Virginia Vega-Warner, Pawaree Saisawat, Katrina A Diaz, Humphrey Fang,[...]. Kidney Int 2014
50
18

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
9

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
Asaf Vivante, Stefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, Friedhelm Hildebrandt. Pediatr Nephrol 2014
97
9

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Andrew Kirby, Andreas Gnirke, David B Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel, Chun Ye, Daniel Aird, Christine Stevens, James T Robinson,[...]. Nat Genet 2013
134
9

The expanding phenotypic spectra of kidney diseases: insights from genetic studies.
Marijn F Stokman, Kirsten Y Renkema, Rachel H Giles, Franz Schaefer, Nine V A M Knoers, Albertien M van Eerde. Nat Rev Nephrol 2016
37
24

Chronic Kidney Disease.
Angela C Webster, Evi V Nagler, Rachael L Morton, Philip Masson. Lancet 2017
865
9

Mutations in PAX2 associate with adult-onset FSGS.
Moumita Barua, Emilia Stellacci, Lorenzo Stella, Astrid Weins, Giulio Genovese, Valentina Muto, Viviana Caputo, Hakan R Toka, Victoria T Charoonratana, Marco Tartaglia,[...]. J Am Soc Nephrol 2014
53
15

Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression.
Sabrina Giglio, Aldesia Provenzano, Benedetta Mazzinghi, Francesca Becherucci, Laura Giunti, Giulia Sansavini, Fiammetta Ravaglia, Rosa Maria Roperto, Silvia Farsetti, Elisa Benetti,[...]. J Am Soc Nephrol 2015
57
14

Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
Fang Wang, Yanqin Zhang, Jianhua Mao, Zihua Yu, Zhuwen Yi, Li Yu, Jun Sun, Xiuxiu Wei, Fangrui Ding, Hongwen Zhang,[...]. Pediatr Nephrol 2017
42
19

A systematic approach to mapping recessive disease genes in individuals from outbred populations.
Friedhelm Hildebrandt, Saskia F Heeringa, Franz Rüschendorf, Massimo Attanasio, Gudrun Nürnberg, Christian Becker, Dominik Seelow, Norbert Huebner, Gil Chernin, Christopher N Vlangos,[...]. PLoS Genet 2009
117
8

Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy.
Jan Halbritter, Jonathan D Porath, Katrina A Diaz, Daniela A Braun, Stefan Kohl, Moumita Chaki, Susan J Allen, Neveen A Soliman, Friedhelm Hildebrandt, Edgar A Otto. Hum Genet 2013
129
8

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.
Elizabeth J Brown, Johannes S Schlöndorff, Daniel J Becker, Hiroyasu Tsukaguchi, Stephen J Tonna, Andrea L Uscinski, Henry N Higgs, Joel M Henderson, Martin R Pollak. Nat Genet 2010
298
8

Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
Sheila Santín, Gemma Bullich, Bárbara Tazón-Vega, Rafael García-Maset, Isabel Giménez, Irene Silva, Patricia Ruíz, José Ballarín, Roser Torra, Elisabet Ars. Clin J Am Soc Nephrol 2011
124
8

Association of trypanolytic ApoL1 variants with kidney disease in African Americans.
Giulio Genovese, David J Friedman, Michael D Ross, Laurence Lecordier, Pierrick Uzureau, Barry I Freedman, Donald W Bowden, Carl D Langefeld, Taras K Oleksyk, Andrea L Uscinski Knob,[...]. Science 2010
8

Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.
Weizhen Tan, Svjetlana Lovric, Shazia Ashraf, Jia Rao, David Schapiro, Merlin Airik, Shirlee Shril, Heon Yung Gee, Michelle Baum, Ghaleb Daouk,[...]. Pediatr Nephrol 2018
16
50

Genetic basis of human congenital anomalies of the kidney and urinary tract.
Simone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, Ali G Gharavi. J Clin Invest 2018
33
24


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.