A citation-based method for searching scientific literature

Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
Times Cited: 58







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



Times Cited
  Times     Co-cited
Similarity


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
199
46

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

Exploring the genetic basis of early-onset chronic kidney disease.
Asaf Vivante, Friedhelm Hildebrandt. Nat Rev Nephrol 2016
155
34

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
92
34

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
74
31

Rare inherited kidney diseases: challenges, opportunities, and perspectives.
Olivier Devuyst, Nine V A M Knoers, Giuseppe Remuzzi, Franz Schaefer. Lancet 2014
119
29

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
325
20

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
93
18

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
46
23

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
123
15

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
42
21

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
902
15

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

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
147
15

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
111
13

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
170
13

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
13

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
44
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
132
12

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
33
21

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
23
30

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
25
28

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
76
12

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
20
30

A multidisciplinary renal genetics clinic improves patient diagnosis.
Andrew Mallett, Lindsay F Fowles, Julie McGaughran, Helen Healy, Chirag Patel. Med J Aust 2016
17
35

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
54
11

Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases.
Emilie Cornec-Le Gall, Vicente E Torres, Peter C Harris. J Am Soc Nephrol 2018
104
10

Genetic kidney diseases.
Friedhelm Hildebrandt. Lancet 2010
188
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
40
15

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
46
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
146
10

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
10

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A Fasel, Ekaterina Batourina, Matthew G Sampson,[...]. Nat Genet 2019
63
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
134
8

Coming of age: ten years of next-generation sequencing technologies.
Sara Goodwin, John D McPherson, W Richard McCombie. Nat Rev Genet 2016
8

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
812
8

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
70
8

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
111
8

Individuals with a family history of ESRD are a high-risk population for CKD: implications for targeted surveillance and intervention activities.
William M McClellan, Scott G Satko, Elisa Gladstone, Jenna O Krisher, Andrew S Narva, Barry I Freedman. Am J Kidney Dis 2009
26
19

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
114
8

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
86
8

Lessons learned from a multidisciplinary renal genetics clinic.
S Alkanderi, L M Yates, S A Johnson, J A Sayer. QJM 2017
15
33

Renal genetics in Australia: Kidney medicine in the genomic age.
Kushani Jayasinghe, Catherine Quinlan, Zornitza Stark, Chirag Patel, Amali Mallawaarachchi, Louise Wardrop, Peter G Kerr, Peter Trnka, Andrew J Mallett. Nephrology (Carlton) 2019
10
50

Personalized medicine in chronic kidney disease by detection of monogenic mutations.
Dervla M Connaughton, Friedhelm Hildebrandt. Nephrol Dial Transplant 2020
23
21

Reverse Phenotyping after Whole-Exome Sequencing in Steroid-Resistant Nephrotic Syndrome.
Samuela Landini, Benedetta Mazzinghi, Francesca Becherucci, Marco Allinovi, Aldesia Provenzano, Viviana Palazzo, Fiammetta Ravaglia, Rosangela Artuso, Emanuele Bosi, Stefano Stagi,[...]. Clin J Am Soc Nephrol 2020
25
20

Clinical impact of genomic testing in patients with suspected monogenic kidney disease.
Kushani Jayasinghe, Zornitza Stark, Peter G Kerr, Clara Gaff, Melissa Martyn, John Whitlam, Belinda Creighton, Elizabeth Donaldson, Matthew Hunter, Anna Jarmolowicz,[...]. Genet Med 2021
17
29

Clinical Genetic Screening in Adult Patients with Kidney Disease.
Enrico Cocchi, Jordan Gabriela Nestor, Ali G Gharavi. Clin J Am Soc Nephrol 2020
17
29

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
159
6

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
Laurence Heidet, Vincent Morinière, Charline Henry, Lara De Tomasi, Madeline Louise Reilly, Camille Humbert, Olivier Alibeu, Cécile Fourrage, Christine Bole-Feysot, Patrick Nitschké,[...]. J Am Soc Nephrol 2017
54
7

Chronic Kidney Disease.
Angela C Webster, Evi V Nagler, Rachael L Morton, Philip Masson. Lancet 2017
6


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.