A citation-based method for searching scientific literature

Sarah A Howles, Akira Wiberg, Michelle Goldsworthy, Asha L Bayliss, Anna K Gluck, Michael Ng, Emily Grout, Chizu Tanikawa, Yoichiro Kamatani, Chikashi Terao, Atsushi Takahashi, Michiaki Kubo, Koichi Matsuda, Rajesh V Thakker, Benjamin W Turney, Dominic Furniss. Nat Commun 2019
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Common and rare variants associated with kidney stones and biochemical traits.
Asmundur Oddsson, Patrick Sulem, Hannes Helgason, Vidar O Edvardsson, Gudmar Thorleifsson, Gardar Sveinbjörnsson, Eik Haraldsdottir, Gudmundur I Eyjolfsson, Olof Sigurdardottir, Isleifur Olafsson,[...]. Nat Commun 2015
80
61

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.
Gudmar Thorleifsson, Hilma Holm, Vidar Edvardsson, G Bragi Walters, Unnur Styrkarsdottir, Daniel F Gudbjartsson, Patrick Sulem, Bjarni V Halldorsson, Femmie de Vegt, Frank C H d'Ancona,[...]. Nat Genet 2009
177
44

Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis.
Jan Halbritter, Michelle Baum, Ann Marie Hynes, Sarah J Rice, David T Thwaites, Zoran S Gucev, Brittany Fisher, Leslie Spaneas, Jonathan D Porath, Daniela A Braun,[...]. J Am Soc Nephrol 2015
96
44

Prevalence of kidney stones in the United States.
Charles D Scales, Alexandria C Smith, Janet M Hanley, Christopher S Saigal. Eur Urol 2012
38

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
65
33

Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis.
Daniela Anne Braun, Jennifer Ashley Lawson, Heon Yung Gee, Jan Halbritter, Shirlee Shril, Weizhen Tan, Deborah Stein, Ari J Wassner, Michael A Ferguson, Zoran Gucev,[...]. Clin J Am Soc Nephrol 2016
64
33



Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population.
Chizu Tanikawa, Yoichiro Kamatani, Chikashi Terao, Masayuki Usami, Atsushi Takahashi, Yukihide Momozawa, Kichiya Suzuki, Soichi Ogishima, Atsushi Shimizu, Mamoru Satoh,[...]. J Am Soc Nephrol 2019
12
41

Family history and risk of kidney stones.
G C Curhan, W C Willett, E B Rimm, M J Stampfer. J Am Soc Nephrol 1997
173
27

A Twin Study of Genetic Influences on Nephrolithiasis in Women and Men.
David S Goldfarb, Ally R Avery, Lada Beara-Lasic, Glen E Duncan, Jack Goldberg. Kidney Int Rep 2018
17
29

Mutations in CYP24A1 and idiopathic infantile hypercalcemia.
Karl P Schlingmann, Martin Kaufmann, Stefanie Weber, Andrew Irwin, Caroline Goos, Ulrike John, Joachim Misselwitz, Günter Klaus, Eberhard Kuwertz-Bröking, Henry Fehrenbach,[...]. N Engl J Med 2011
337
27

Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.
Daniel F Gudbjartsson, Hilma Holm, Olafur S Indridason, Gudmar Thorleifsson, Vidar Edvardsson, Patrick Sulem, Femmie de Vegt, Frank C H d'Ancona, Martin den Heijer, Jack F M Wetzels,[...]. PLoS Genet 2010
130
22

A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1.
Yuji Urabe, Chizu Tanikawa, Atsushi Takahashi, Yukinori Okada, Takashi Morizono, Tatsuhiko Tsunoda, Naoyuki Kamatani, Kenjiro Kohri, Kazuaki Chayama, Michiaki Kubo,[...]. PLoS Genet 2012
45
22

Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis.
Debayan Dasgupta, Mark J Wee, Monica Reyes, Yuwen Li, Peter J Simm, Amita Sharma, Karl-Peter Schlingmann, Marco Janner, Andrew Biggin, Joanna Lazier,[...]. J Am Soc Nephrol 2014
70
22

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.
D B Simon, Y Lu, K A Choate, H Velazquez, E Al-Sabban, M Praga, G Casari, A Bettinelli, G Colussi, J Rodriguez-Soriano,[...]. Science 1999
775
22

Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.
Martin Konrad, Andre Schaller, Dominik Seelow, Amit V Pandey, Siegfried Waldegger, Annegret Lesslauer, Helga Vitzthum, Yoshiro Suzuki, John M Luk, Christian Becker,[...]. Am J Hum Genet 2006
307
22

The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II.
S D Cramer, P M Ferree, K Lin, D S Milliner, R P Holmes. Hum Mol Genet 1999
117
22

Kidney stones: a global picture of prevalence, incidence, and associated risk factors.
Victoriano Romero, Haluk Akpinar, Dean G Assimos. Rev Urol 2010
487
22

Kidney stones.
Saeed R Khan, Margaret S Pearle, William G Robertson, Giovanni Gambaro, Benjamin K Canales, Steeve Doizi, Olivier Traxer, Hans-Göran Tiselius. Nat Rev Dis Primers 2016
174
22

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
16

An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
16

Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations.
N Rungroj, C Nettuwakul, N Sawasdee, S Sangnual, N Deejai, R A Misgar, A Pasena, S Khositseth, S Kirdpon, S Sritippayawan,[...]. Clin Genet 2018
24
16

Medical management of kidney stones: AUA guideline.
Margaret S Pearle, David S Goldfarb, Dean G Assimos, Gary Curhan, Cynthia J Denu-Ciocca, Brian R Matlaga, Manoj Monga, Kristina L Penniston, Glenn M Preminger, Thomas M T Turk,[...]. J Urol 2014
369
16

Phenotype and genotype characterization of adenine phosphoribosyltransferase deficiency.
Guillaume Bollée, Cécile Dollinger, Lucile Boutaud, Delphine Guillemot, Albert Bensman, Jérôme Harambat, Patrice Deteix, Michel Daudon, Bertrand Knebelmann, Irène Ceballos-Picot. J Am Soc Nephrol 2010
63
16

Mutations in SLC26A1 Cause Nephrolithiasis.
Heon Yung Gee, Ikhyun Jun, Daniela A Braun, Jennifer A Lawson, Jan Halbritter, Shirlee Shril, Caleb P Nelson, Weizhen Tan, Deborah Stein, Ari J Wassner,[...]. Am J Hum Genet 2016
23
16

Genetic predisposition to formation of calcium oxalate renal calculi.
M Resnick, D B Pridgen, H O Goodman. N Engl J Med 1968
133
16

Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter.
Dominique Prié, Virginie Huart, Naziha Bakouh, Gabrielle Planelles, Olivier Dellis, Bénédicte Gérard, Philippe Hulin, François Benqué-Blanchet, Caroline Silve, Bernard Grandchamp,[...]. N Engl J Med 2002
220
16

Idiopathic hypercalciuria and formation of calcium renal stones.
Fredric L Coe, Elaine M Worcester, Andrew P Evan. Nat Rev Nephrol 2016
75
16

Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.
Katharina Hopp, Andrea G Cogal, Eric J Bergstralh, Barbara M Seide, Julie B Olson, Alicia M Meek, John C Lieske, Dawn S Milliner, Peter C Harris. J Am Soc Nephrol 2015
95
16

Kidney stone disease.
Fredric L Coe, Andrew Evan, Elaine Worcester. J Clin Invest 2005
387
16

Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.
K Ichida, Y Amaya, N Kamatani, T Nishino, T Hosoya, O Sakai. J Clin Invest 1997
87
16

Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia.
Hirotaka Matsuo, Toshinori Chiba, Shushi Nagamori, Akiyoshi Nakayama, Hideharu Domoto, Kanokporn Phetdee, Pattama Wiriyasermkul, Yuichi Kikuchi, Takashi Oda, Junichiro Nishiyama,[...]. Am J Hum Genet 2008
237
16

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.
Karl P Schlingmann, Justyna Ruminska, Martin Kaufmann, Ismail Dursun, Monica Patti, Birgitta Kranz, Ewa Pronicka, Elzbieta Ciara, Teoman Akcay, Derya Bulus,[...]. J Am Soc Nephrol 2016
104
16

A common molecular basis for three inherited kidney stone diseases.
S E Lloyd, S H Pearce, S E Fisher, K Steinmeyer, B Schwappach, S J Scheinman, B Harding, A Bolino, M Devoto, P Goodyer,[...]. Nature 1996
551
16

Acidosis and Deafness in Patients with Recessive Mutations in FOXI1.
Sven Enerbäck, Daniel Nilsson, Noel Edwards, Mikael Heglind, Sumaya Alkanderi, Emma Ashton, Asma Deeb, Feras E B Kokash, Abdul R A Bakhsh, William Van't Hoff,[...]. J Am Soc Nephrol 2018
40
16

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor.
S H Pearce, C Williamson, O Kifor, M Bai, M G Coulthard, M Davies, N Lewis-Barned, D McCredie, H Powell, P Kendall-Taylor,[...]. N Engl J Med 1996
372
16

Kidney Disease in Adenine Phosphoribosyltransferase Deficiency.
Hrafnhildur Linnet Runolfsdottir, Runolfur Palsson, Inger M Agustsdottir, Olafur S Indridason, Vidar O Edvardsson. Am J Kidney Dis 2016
32
16

Hereditary hypophosphatemic rickets with hypercalciuria.
M Tieder, D Modai, R Samuel, R Arie, A Halabe, I Bab, D Gabizon, U A Liberman. N Engl J Med 1985
188
16

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.
F E Karet, K E Finberg, R D Nelson, A Nayir, H Mocan, S A Sanjad, J Rodriguez-Soriano, F Santos, C W Cremers, A Di Pietro,[...]. Nat Genet 1999
500
16

Hereditary causes of kidney stones and chronic kidney disease.
Vidar O Edvardsson, David S Goldfarb, John C Lieske, Lada Beara-Lasic, Franca Anglani, Dawn S Milliner, Runolfur Palsson. Pediatr Nephrol 2013
120
16

Genome-wide analysis of genes related to kidney stone formation and elimination in the calcium oxalate nephrolithiasis model mouse: detection of stone-preventive factors and involvement of macrophage activity.
Atsushi Okada, Takahiro Yasui, Shuzo Hamamoto, Masahito Hirose, Yasue Kubota, Yasunori Itoh, Keiichi Tozawa, Yutaro Hayashi, Kenjiro Kohri. J Bone Miner Res 2009
62
16

Genetics of common complex kidney stone disease: insights from genome-wide association studies.
Runolfur Palsson, Olafur S Indridason, Vidar O Edvardsson, Asmundur Oddsson. Urolithiasis 2019
14
21

SLC2A9 influences uric acid concentrations with pronounced sex-specific effects.
Angela Döring, Christian Gieger, Divya Mehta, Henning Gohlke, Holger Prokisch, Stefan Coassin, Guido Fischer, Kathleen Henke, Norman Klopp, Florian Kronenberg,[...]. Nat Genet 2008
289
16

PhenoScanner: a database of human genotype-phenotype associations.
James R Staley, James Blackshaw, Mihir A Kamat, Steve Ellis, Praveen Surendran, Benjamin B Sun, Dirk S Paul, Daniel Freitag, Stephen Burgess, John Danesh,[...]. Bioinformatics 2016
339
16

Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT.
L Feliubadaló, M Font, J Purroy, F Rousaud, X Estivill, V Nunes, E Golomb, M Centola, I Aksentijevich, Y Kreiss,[...]. Nat Genet 1999
232
16

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.
D B Simon, F E Karet, J Rodriguez-Soriano, J H Hamdan, A DiPietro, H Trachtman, S A Sanjad, R P Lifton. Nat Genet 1996
621
16

Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.
Bettina Lorenz-Depiereux, Anna Benet-Pages, Gertrud Eckstein, Yardena Tenenbaum-Rakover, Janine Wagenstaller, Dov Tiosano, Ruth Gershoni-Baruch, Norbert Albers, Peter Lichtner, Dirk Schnabel,[...]. Am J Hum Genet 2006
219
16

Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine.
M J Calonge, P Gasparini, J Chillarón, M Chillón, M Gallucci, F Rousaud, L Zelante, X Testar, B Dallapiccola, F Di Silverio. Nat Genet 1994
306
16

Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis.
Ali Amar, Amar J Majmundar, Ihsan Ullah, Ayesha Afzal, Daniela A Braun, Shirlee Shril, Ankana Daga, Tilman Jobst-Schwan, Mumtaz Ahmad, John A Sayer,[...]. Hum Genet 2019
12
25


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.