A citation-based method for searching scientific literature

Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
Times Cited: 46







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



Times Cited
  Times     Co-cited
Similarity


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
39

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
39

Exploring the genetic basis of early-onset chronic kidney disease.
Asaf Vivante, Friedhelm Hildebrandt. Nat Rev Nephrol 2016
134
36

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
32

Rare inherited kidney diseases: challenges, opportunities, and perspectives.
Olivier Devuyst, Nine V A M Knoers, Giuseppe Remuzzi, Franz Schaefer. Lancet 2014
110
28

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
23

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
21

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
19

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
19

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
22

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
17

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
17

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

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.
Oliver Gross, Christoph Licht, Hans J Anders, Bernd Hoppe, Bodo Beck, Burkhard Tönshoff, Britta Höcker, Simone Wygoda, Jochen H H Ehrich, Lars Pape,[...]. Kidney Int 2012
154
15

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
15

Renal replacement therapy for rare diseases affecting the kidney: an analysis of the ERA-EDTA Registry.
Elke Wühl, Karlijn J van Stralen, Christoph Wanner, Gema Ariceta, James Goya Heaf, Anna K Bjerre, Runolfur Palsson, Gabrielle Duneau, Andries J Hoitsma, Pietro Ravani,[...]. Nephrol Dial Transplant 2014
31
22

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
15

Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS.
Tony Yao, Khalil Udwan, Rohan John, Akanchaya Rana, Amirreza Haghighi, Lizhen Xu, Saidah Hack, Heather N Reich, Michelle Adrienne Hladunewich, Daniel C Cattran,[...]. Clin J Am Soc Nephrol 2019
34
20

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
20

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
13

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
33

Chronic kidney disease: global dimension and perspectives.
Vivekanand Jha, Guillermo Garcia-Garcia, Kunitoshi Iseki, Zuo Li, Saraladevi Naicker, Brett Plattner, Rajiv Saran, Angela Yee-Moon Wang, Chih-Wei Yang. Lancet 2013
13

Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
Ségolène Aymé, Detlef Bockenhauer, Simon Day, Olivier Devuyst, Lisa M Guay-Woodford, Julie R Ingelfinger, Jon B Klein, Nine V A M Knoers, Ronald D Perrone, Julia Roberts,[...]. Kidney Int 2017
16
31

Coming of age: ten years of next-generation sequencing technologies.
Sara Goodwin, John D McPherson, W Richard McCombie. Nat Rev Genet 2016
10

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
10

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.
Ankana Daga, Amar J Majmundar, Daniela A Braun, Heon Yung Gee, Jennifer A Lawson, Shirlee Shril, Tilman Jobst-Schwan, Asaf Vivante, David Schapiro, Weizhen Tan,[...]. Kidney Int 2018
57
10

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
10

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
10

Genetic kidney diseases.
Friedhelm Hildebrandt. Lancet 2010
169
10

NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD.
Rozemarijn Snoek, Jessica van Setten, Brendan J Keating, Ajay K Israni, Pamala A Jacobson, William S Oetting, Arthur J Matas, Roslyn B Mannon, Zhongyang Zhang, Weijia Zhang,[...]. J Am Soc Nephrol 2018
33
15

Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome.
Hugh J McCarthy, Agnieszka Bierzynska, Matt Wherlock, Milos Ognjanovic, Larissa Kerecuk, Shivaram Hegde, Sally Feather, Rodney D Gilbert, Leah Krischock, Caroline Jones,[...]. Clin J Am Soc Nephrol 2013
110
10

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
13

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
10

Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.
Clifford E Kashtan, Jie Ding, Guido Garosi, Laurence Heidet, Laura Massella, Koichi Nakanishi, Kandai Nozu, Alessandra Renieri, Michelle Rheault, Fang Wang,[...]. Kidney Int 2018
68
10

HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum.
Rhian L Clissold, Alexander J Hamilton, Andrew T Hattersley, Sian Ellard, Coralie Bingham. Nat Rev Nephrol 2015
115
8

Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background.
Elena Bresin, Erica Daina, Marina Noris, Federica Castelletti, Rumen Stefanov, Prudence Hill, Timothy H J Goodship, Giuseppe Remuzzi. Clin J Am Soc Nephrol 2006
157
8

A multidisciplinary renal genetics clinic improves patient diagnosis.
Andrew Mallett, Lindsay F Fowles, Julie McGaughran, Helen Healy, Chirag Patel. Med J Aust 2016
12
33

Chronic Kidney Disease.
Angela C Webster, Evi V Nagler, Rachael L Morton, Philip Masson. Lancet 2017
865
8

Clinical application of whole-exome sequencing across clinical indications.
Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan,[...]. Genet Med 2016
433
8

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.
Shay Tzur, Saharon Rosset, Revital Shemer, Guennady Yudkovsky, Sara Selig, Ayele Tarekegn, Endashaw Bekele, Neil Bradman, Walter G Wasser, Doron M Behar,[...]. Hum Genet 2010
391
8

Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.
Jennifer E Posey, Tamar Harel, Pengfei Liu, Jill A Rosenfeld, Regis A James, Zeynep H Coban Akdemir, Magdalena Walkiewicz, Weimin Bi, Rui Xiao, Yan Ding,[...]. N Engl J Med 2017
316
8

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
8

Differentiating Primary, Genetic, and Secondary FSGS in Adults: A Clinicopathologic Approach.
An S De Vriese, Sanjeev Sethi, Karl A Nath, Richard J Glassock, Fernando C Fervenza. J Am Soc Nephrol 2018
61
8

The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.
Hila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, David A Fasel, Adele Mitrotti, Rik Westland, Louise Bier, Chunhua Weng, Zhong Ren, Brett Copeland,[...]. Ann Intern Med 2019
21
19

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

Sequencing studies in human genetics: design and interpretation.
David B Goldstein, Andrew Allen, Jonathan Keebler, Elliott H Margulies, Steven Petrou, Slavé Petrovski, Shamil Sunyaev. Nat Rev Genet 2013
165
8

Genetic testing in steroid-resistant nephrotic syndrome: when and how?
Svjetlana Lovric, Shazia Ashraf, Weizhen Tan, Friedhelm Hildebrandt. Nephrol Dial Transplant 2016
104
8

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
9

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome.
Mathieu Lemaire, Véronique Frémeaux-Bacchi, Franz Schaefer, Murim Choi, Wai Ho Tang, Moglie Le Quintrec, Fadi Fakhouri, Sophie Taque, François Nobili, Frank Martinez,[...]. Nat Genet 2013
279
8

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
8


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.