A citation-based method for searching scientific literature

Judy Savige, Francesca Ariani, Francesca Mari, Mirella Bruttini, Alessandra Renieri, Oliver Gross, Constantinos Deltas, Frances Flinter, Jie Ding, Daniel P Gale, Mato Nagel, Michael Yau, Lev Shagam, Roser Torra, Elisabet Ars, Julia Hoefele, Guido Garosi, Helen Storey. Pediatr Nephrol 2019
Times Cited: 45







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



Times Cited
  Times     Co-cited
Similarity


Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy.
Judy Savige, Martin Gregory, Oliver Gross, Clifford Kashtan, Jie Ding, Frances Flinter. J Am Soc Nephrol 2013
163
51

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
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
42

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.
Jean Philippe Jais, Bertrand Knebelmann, Iannis Giatras, Mario DE Marchi, Gianfranco Rizzoni, Alessandra Renieri, Manfred Weber, Oliver Gross, Kai-Olaf Netzer, Frances Flinter,[...]. J Am Soc Nephrol 2000
295
35

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study.
Jean Philippe Jais, Bertrand Knebelmann, Iannis Giatras, Mario De Marchi, Gianfranco Rizzoni, Alessandra Renieri, Manfred Weber, Oliver Gross, Kai-Olaf Netzer, Frances Flinter,[...]. J Am Soc Nephrol 2003
227
35

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
35

Evidence of digenic inheritance in Alport syndrome.
Maria Antonietta Mencarelli, Laurence Heidet, Helen Storey, Michel van Geel, Bertrand Knebelmann, Chiara Fallerini, Nunzia Miglietti, Maria Fatima Antonucci, Francesco Cetta, John A Sayer,[...]. J Med Genet 2015
73
28

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
28

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
26

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases.
C Fallerini, L Dosa, R Tita, D Del Prete, S Feriozzi, G Gai, M Clementi, A La Manna, N Miglietti, R Mancini,[...]. Clin Genet 2014
72
24

Alport Syndrome in Women and Girls.
Judy Savige, Deb Colville, Michelle Rheault, Susie Gear, Rachel Lennon, Sharon Lagas, Moira Finlay, Frances Flinter. Clin J Am Soc Nephrol 2016
41
24

X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations.
Judith Savige, Helen Storey, Hae Il Cheong, Hee Gyung Kang, Eujin Park, Pascale Hilbert, Anton Persikov, Carmen Torres-Fernandez, Elisabet Ars, Roser Torra,[...]. PLoS One 2016
34
29

Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.
Naohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, Naoya Morisada, Yoshimi Nozu, Ming Juan Ye, Aya Imafuku, Kenichiro Miura, Tomohiko Yamamura, Shogo Minamikawa,[...]. Clin J Am Soc Nephrol 2016
41
21

Genotype-phenotype correlation in X-linked Alport syndrome.
Mir Reza Bekheirnia, Berenice Reed, Martin C Gregory, Kim McFann, Alireza Abdollah Shamshirsaz, Amirali Masoumi, Robert W Schrier. J Am Soc Nephrol 2010
102
20

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy.
Konstantinos Voskarides, Loukas Damianou, Vassos Neocleous, Ioanna Zouvani, Stalo Christodoulidou, Valsamakis Hadjiconstantinou, Kyriacos Ioannou, Yiannis Athanasiou, Charalampos Patsias, Efstathios Alexopoulos,[...]. J Am Soc Nephrol 2007
125
20

Improving mutation screening in familial hematuric nephropathies through next generation sequencing.
Vincent Morinière, Karin Dahan, Pascale Hilbert, Marieline Lison, Said Lebbah, Alexandra Topa, Christine Bole-Feysot, Solenn Pruvost, Patrick Nitschke, Emmanuelle Plaisier,[...]. J Am Soc Nephrol 2014
76
20

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
20

Thin basement membrane nephropathy.
Judy Savige, Kesha Rana, Stephen Tonna, Mark Buzza, Hayat Dagher, Yan Yan Wang. Kidney Int 2003
132
17

Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome.
Oliver Gross, Clifford E Kashtan, Michelle N Rheault, Frances Flinter, Judith Savige, Jeffrey H Miner, Roser Torra, Elisabet Ars, Constantinos Deltas, Isavella Savva,[...]. Nephrol Dial Transplant 2017
28
28


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
23

Alport syndrome: impact of digenic inheritance in patients management.
C Fallerini, M Baldassarri, E Trevisson, V Morbidoni, A La Manna, R Lazzarin, A Pasini, G Barbano, A R Pinciaroli, G Garosi,[...]. Clin Genet 2017
24
29

COL4A3/COL4A4 mutations and features in individuals with autosomal recessive Alport syndrome.
Helen Storey, Judy Savige, Vanessa Sivakumar, Stephen Abbs, Frances A Flinter. J Am Soc Nephrol 2013
61
15

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.
Alkis Pierides, Konstantinos Voskarides, Yiannis Athanasiou, Kyriacos Ioannou, Loukas Damianou, Maria Arsali, Michalis Zavros, Michael Pierides, Vasilios Vargemezis, Charalambos Patsias,[...]. Nephrol Dial Transplant 2009
82
15

COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi, Ioanelli Petrou, Isavella Savva, Avraam Elia, Yiannis Athanasiou, Androulla Pastelli, Maria Kkolou, Michalis Hadjigavriel,[...]. BMC Nephrol 2018
18
38

Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: impact on clinical counselling.
Oliver Gross, Kai-Olaf Netzer, Romy Lambrecht, Stefan Seibold, Manfred Weber. Nephrol Dial Transplant 2002
142
15

A review of clinical characteristics and genetic backgrounds in Alport syndrome.
Kandai Nozu, Koichi Nakanishi, Yoshifusa Abe, Tomohiro Udagawa, Shinichi Okada, Takayuki Okamoto, Hiroshi Kaito, Katsuyoshi Kanemoto, Anna Kobayashi, Eriko Tanaka,[...]. Clin Exp Nephrol 2019
39
17

New therapeutic options for Alport syndrome.
Roser Torra, Mónica Furlano. Nephrol Dial Transplant 2019
13
53

Identification of mutations in the COL4A5 collagen gene in Alport syndrome.
D F Barker, S L Hostikka, J Zhou, L T Chow, A R Oliphant, S C Gerken, M C Gregory, M H Skolnick, C L Atkin, K Tryggvason. Science 1990
630
13

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome.
T Mochizuki, H H Lemmink, M Mariyama, C Antignac, M C Gubler, Y Pirson, C Verellen-Dumoulin, B Chan, C H Schröder, H J Smeets. Nat Genet 1994
369
13


Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research Collaborative.
Clifford E Kashtan, Jie Ding, Martin Gregory, Oliver Gross, Laurence Heidet, Bertrand Knebelmann, Michelle Rheault, Christoph Licht. Pediatr Nephrol 2013
63
13

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
13

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations.
Johanna Temme, Frederick Peters, Katharina Lange, Yves Pirson, Laurence Heidet, Roser Torra, Jean-Pierre Grunfeld, Manfred Weber, Christoph Licht, Gerhard-Anton Müller,[...]. Kidney Int 2012
75
13

Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain.
Yuya Hashimura, Kandai Nozu, Hiroshi Kaito, Koichi Nakanishi, Xue Jun Fu, Hiromi Ohtsubo, Fusako Hashimoto, Masafumi Oka, Takeshi Ninchoji, Shingo Ishimori,[...]. Kidney Int 2014
41
12

The R229Q mutation in NPHS2 may predispose to proteinuria in thin-basement-membrane nephropathy.
Stephen Tonna, Yan Yan Wang, Diane Wilson, Lin Rigby, Tania Tabone, Richard Cotton, Judy Savige. Pediatr Nephrol 2008
39
12

Cellular origins of type IV collagen networks in developing glomeruli.
Dale R Abrahamson, Billy G Hudson, Larysa Stroganova, Dorin-Bogdan Borza, Patricia L St John. J Am Soc Nephrol 2009
111
11

Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome.
Tomohiko Yamamura, Kandai Nozu, Xue Jun Fu, Yoshimi Nozu, Ming Juan Ye, Akemi Shono, Satoko Yamanouchi, Shogo Minamikawa, Naoya Morisada, Koichi Nakanishi,[...]. Kidney Int Rep 2017
23
21

Natural history of genetically proven autosomal recessive Alport syndrome.
Masafumi Oka, Kandai Nozu, Hiroshi Kaito, Xue Jun Fu, Koichi Nakanishi, Yuya Hashimura, Naoya Morisada, Kunimasa Yan, Masafumi Matsuo, Norishige Yoshikawa,[...]. Pediatr Nephrol 2014
31
16

A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases.
Gemma Bullich, Andrea Domingo-Gallego, Iván Vargas, Patricia Ruiz, Laura Lorente-Grandoso, Mónica Furlano, Gloria Fraga, Álvaro Madrid, Gema Ariceta, Mar Borregán,[...]. Kidney Int 2018
39
12

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
14

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
11

COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome.
Ilaria Longo, Paola Porcedda, Francesca Mari, Daniela Giachino, Ilaria Meloni, Carla Deplano, Alfredo Brusco, Maurizio Bosio, Laura Massella, Giancarlo Lavoratti,[...]. Kidney Int 2002
139
11

Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life.
Constantinos Deltas, Isavella Savva, Konstantinos Voskarides, Louiza Papazachariou, Alkis Pierides. Nephron 2015
30
16

Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults.
Olivier Gribouval, Olivia Boyer, Aurélie Hummel, Jacques Dantal, Frank Martinez, Rebecca Sberro-Soussan, Isabelle Etienne, Dominique Chauveau, Michel Delahousse, Arnaud Lionet,[...]. Kidney Int 2018
18
27

Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
L Papazachariou, G Papagregoriou, D Hadjipanagi, P Demosthenous, K Voskarides, C Koutsofti, K Stylianou, P Ioannou, D Xydakis, I Tzanakis,[...]. Clin Genet 2017
16
31

Alport's syndrome, Goodpasture's syndrome, and type IV collagen.
Billy G Hudson, Karl Tryggvason, Munirathinam Sundaramoorthy, Eric G Neilson. N Engl J Med 2003
572
11

Alport syndrome--insights from basic and clinical research.
Jenny Kruegel, Diana Rubel, Oliver Gross. Nat Rev Nephrol 2013
119
11

Type of PKD1 mutation influences renal outcome in ADPKD.
Emilie Cornec-Le Gall, Marie-Pierre Audrézet, Jian-Min Chen, Maryvonne Hourmant, Marie-Pascale Morin, Régine Perrichot, Christophe Charasse, Bassem Whebe, Eric Renaudineau, Philippe Jousset,[...]. J Am Soc Nephrol 2013
247
11

Genetic heterogeneity of Alport syndrome.
J Feingold, E Bois, A Chompret, M Broyer, M C Gubler, J P Grünfeld. Kidney Int 1985
163
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.