A citation-based method for searching scientific literature

Cinthia Carolina Stempin, Romina Celeste Geysels, Sunmi Park, Luz Maria Palacios, Ximena Volpini, Claudia Cristina Motran, Eva Virginia Acosta Rodríguez, Juan Pablo Nicola, Sheue-Yann Cheng, Claudia Gabriela Pellizas, Laura Fozzatti. Cancers (Basel) 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


A Carboxy-Terminal Monoleucine-Based Motif Participates in the Basolateral Targeting of the Na+/I- Symporter.
Mariano Martín, Carlos Pablo Modenutti, Victoria Peyret, Romina Celeste Geysels, Elisabeth Darrouzet, Thierry Pourcher, Ana María Masini-Repiso, Marcelo Adrián Martí, Nancy Carrasco, Juan Pablo Nicola. Endocrinology 2019
19
60

Functional characterization of BRCA1 gene variants by mini-gene splicing assay.
Ane Y Steffensen, Mette Dandanell, Lars Jønson, Bent Ejlertsen, Anne-Marie Gerdes, Finn C Nielsen, Thomas vO Hansen. Eur J Hum Genet 2014
48
60

The Sodium/Iodide Symporter (NIS): Molecular Physiology and Preclinical and Clinical Applications.
Silvia Ravera, Andrea Reyna-Neyra, Giuseppe Ferrandino, L Mario Amzel, Nancy Carrasco. Annu Rev Physiol 2017
110
60

Sodium/Iodide Symporter Mutant V270E Causes Stunted Growth but No Cognitive Deficiency.
Juan Pablo Nicola, Andrea Reyna-Neyra, Paul Saenger, David F Rodriguez-Buritica, José David Gamez Godoy, Radhika Muzumdar, L Mario Amzel, Nancy Carrasco. J Clin Endocrinol Metab 2015
21
60

A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.
Mariano Martín, Carlos Pablo Modenutti, Mauco Lucas Gil Rosas, Victoria Peyret, Romina Celeste Geysels, Carlos Eduardo Bernal Barquero, Gabriela Sobrero, Liliana Muñoz, Malvina Signorino, Graciela Testa,[...]. J Clin Endocrinol Metab 2021
10
60

The PDZ protein SCRIB regulates sodium/iodide symporter (NIS) expression at the basolateral plasma membrane.
Mariano Martín, Lisa Salleron, Victoria Peyret, Romina Celeste Geysels, Elisabeth Darrouzet, Sabine Lindenthal, Carlos Eduardo Bernal Barquero, Ana María Masini-Repiso, Thierry Pourcher, Juan Pablo Nicola. FASEB J 2021
6
60

Novel Sodium/Iodide Symporter Compound Heterozygous Pathogenic Variants Causing Dyshormonogenic Congenital Hypothyroidism.
Mariano Martín, Carlos Eduardo Bernal Barquero, Romina Celeste Geysels, Patricia Papendieck, Victoria Peyret, Ana María Masini-Repiso, Ana Elena Chiesa, Juan Pablo Nicola. Thyroid 2019
15
60

Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5'-untranslated region in a patient with congenital hypothyroidism.
Juan Pablo Nicola, Magalí Nazar, Caroline Serrano-Nascimento, Francemilson Goulart-Silva, Gabriela Sobrero, Graciela Testa, Maria Tereza Nunes, Liliana Muñoz, Mirta Miras, Ana María Masini-Repiso. J Clin Endocrinol Metab 2011
32
60


Nitric oxide-repressed Forkhead factor FoxE1 expression is involved in the inhibition of TSH-induced thyroid peroxidase levels.
María del Mar Montesinos, Juan Pablo Nicola, Magalí Nazar, Victoria Peyret, Ariel Maximiliano Lucero, Claudia Gabriela Pellizas, Ana María Masini-Repiso. Mol Cell Endocrinol 2016
15
60

Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles.
Zeynep Coban-Akdemir, Janson J White, Xiaofei Song, Shalini N Jhangiani, Jawid M Fatih, Tomasz Gambin, Yavuz Bayram, Ivan K Chinn, Ender Karaca, Jaya Punetha,[...]. Am J Hum Genet 2018
98
60

Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5' splice site in the exon 6.
Cintia E Citterio, Cecilia M Morales, Natacha Bouhours-Nouet, Gloria A Machiavelli, Elena Bueno, Frédérique Gatelais, Regis Coutant, Rogelio González-Sarmiento, Carina M Rivolta, Héctor M Targovnik. Mol Cell Endocrinol 2015
10
40



The Iodide Transport Defect-Causing Y348D Mutation in the Na+/I- Symporter Renders the Protein Intrinsically Inactive and Impairs Its Targeting to the Plasma Membrane.
Andrea Reyna-Neyra, Lara Jung, Mayukh Chakrabarti, Mikel X Suárez, L Mario Amzel, Nancy Carrasco. Thyroid 2021
6
40

The Transcription Factor NF-κB Mediates Thyrotropin-Stimulated Expression of Thyroid Differentiation Markers.
Romina Celeste Geysels, Victoria Peyret, Mariano Martín, Magalí Nazar, Carla Reale, Carlos Eduardo Bernal Barquero, Lucas Miranda, Marcelo Adrián Martí, Pasquale Vito, Ana María Masini-Repiso,[...]. Thyroid 2021
5
40

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism.
Zehra Aycan, Hakan Cangul, Marina Muzza, Veysel N Bas, Laura Fugazzola, V Krishna Chatterjee, Luca Persani, Nadia Schoenmakers. J Clin Endocrinol Metab 2017
41
40

Na+ coordination at the Na2 site of the Na+/I- symporter.
Giuseppe Ferrandino, Juan Pablo Nicola, Yuly E Sánchez, Ignacia Echeverria, Yunlong Liu, L Mario Amzel, Nancy Carrasco. Proc Natl Acad Sci U S A 2016
16
40

Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis.
Fiorella S Belforte, Cintia E Citterio, Graciela Testa, María Cecilia Olcese, Gabriela Sobrero, Mirta B Miras, Héctor M Targovnik, Carina M Rivolta. Mol Cell Endocrinol 2016
4
50

Two novel mutations of the TSH-beta subunit gene underlying congenital central hypothyroidism undetectable in neonatal TSH screening.
María Sonia Baquedano, Marta Ciaccio, Noelia Dujovne, Viviana Herzovich, Yesica Longueira, Diana Monica Warman, Marco A Rivarola, Alicia Belgorosky. J Clin Endocrinol Metab 2010
27
40

Functional Toll-like Receptor 4 Overexpression in Papillary Thyroid Cancer by MAPK/ERK-Induced ETS1 Transcriptional Activity.
Victoria Peyret, Magalí Nazar, Mariano Martín, Amado A Quintar, Elmer A Fernandez, Romina C Geysels, Cesar S Fuziwara, María M Montesinos, Cristina A Maldonado, Pilar Santisteban,[...]. Mol Cancer Res 2018
22
40

Implications of Na+/I- Symporter Transport to the Plasma Membrane for Thyroid Hormonogenesis and Radioiodide Therapy.
Mariano Martín, Romina Celeste Geysels, Victoria Peyret, Carlos Eduardo Bernal Barquero, Ana María Masini-Repiso, Juan Pablo Nicola. J Endocr Soc 2018
18
40

Beyond non-integer Hill coefficients: A novel approach to analyzing binding data, applied to Na+-driven transporters.
Silvia Ravera, Matthias Quick, Juan P Nicola, Nancy Carrasco, L Mario Amzel. J Gen Physiol 2015
13
40

Loss-of-Function Variants in a Hungarian Cohort Reveal Structural Insights on TSH Receptor Maturation and Signaling.
Árpád Lábadi, Elisa Stellaria Grassi, Balázs Gellén, Gunnar Kleinau, Heike Biebermann, Beáta Ruzsa, Giulia Gelmini, Orsolya Rideg, Attila Miseta, Gábor L Kovács,[...]. J Clin Endocrinol Metab 2015
14
40

Novel Compound Heterozygous Pathogenic Mutations of SLC5A5 in a Chinese Patient With Congenital Hypothyroidism.
Cao-Xu Zhang, Jun-Xiu Zhang, Liu Yang, Chang-Run Zhang, Feng Cheng, Rui-Jia Zhang, Ya Fang, Zheng Wang, Feng-Yao Wu, Pei-Zhang Li,[...]. Front Endocrinol (Lausanne) 2021
3
66

Physiological sodium concentrations enhance the iodide affinity of the Na+/I- symporter.
Juan P Nicola, Nancy Carrasco, L Mario Amzel. Nat Commun 2014
24
40

Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital Hypothyroidism.
Harsh Durgia, Adeline K Nicholas, Erik Schoenmakers, Jennifer A Dickens, Dhanapathi Halanaik, Jayaprakash Sahoo, Sadishkumar Kamalanathan, Nadia Schoenmakers. Thyroid 2022
2
100

Phenotypic Variability of Patients With PAX8 Variants Presenting With Congenital Hypothyroidism and Eutopic Thyroid.
Núria Camats, Noelia Baz-Redón, Mónica Fernández-Cancio, María Clemente, Ariadna Campos-Martorell, Nadya Jaimes, María Antolín, Elena Garcia-Arumí, Laura Blasco-Pérez, Ida Paramonov,[...]. J Clin Endocrinol Metab 2021
2
100

Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis.
Rui-Meng Yang, Ming Zhan, Qin-Yi Zhou, Xiao-Ping Ye, Feng-Yao Wu, Mei Dong, Feng Sun, Ya Fang, Rui-Jia Zhang, Chang-Run Zhang,[...]. Genet Med 2021
5
40

The KCNQ1-KCNE2 K⁺ channel is required for adequate thyroid I⁻ uptake.
Kerry Purtell, Monika Paroder-Belenitsky, Andrea Reyna-Neyra, Juan P Nicola, Wade Koba, Eugene Fine, Nancy Carrasco, Geoffrey W Abbott. FASEB J 2012
39
40

Insights of Noncanonical Splice-site Variants on RNA Splicing in Patients With Congenital Hypothyroidism.
Najla Albader, Minjing Zou, Huda A BinEssa, Saba Abdi, Anwar F Al-Enezi, Brian F Meyer, Ali S Alzahrani, Yufei Shi. J Clin Endocrinol Metab 2022
2
100

New genetics in congenital hypothyroidism.
Athanasia Stoupa, Dulanjalee Kariyawasam, Marina Muzza, Tiziana de Filippis, Laura Fugazzola, Michel Polak, Luca Persani, Aurore Carré. Endocrine 2021
15
40

Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology.
Paul van Trotsenburg, Athanasia Stoupa, Juliane Léger, Tilman Rohrer, Catherine Peters, Laura Fugazzola, Alessandra Cassio, Claudine Heinrichs, Veronique Beauloye, Joachim Pohlenz,[...]. Thyroid 2021
71
40

An Intramolecular Ionic Interaction Linking Defective Sodium/Iodide Symporter Transport to the Plasma Membrane and Dyshormonogenic Congenital Hypothyroidism.
Carlos Eduardo Bernal Barquero, Mariano Martín, Romina Celeste Geysels, Victoria Peyret, Patricia Papendieck, Ana María Masini-Repiso, Ana Elena Chiesa, Juan Pablo Nicola. Thyroid 2022
2
100


The Response of Prostate Smooth Muscle Cells to Testosterone Is Determined by the Subcellular Distribution of the Androgen Receptor.
Nahuel Peinetti, María Victoria Scalerandi, Mariana Micaela Cuello Rubio, Carolina Leimgruber, Juan Pablo Nicola, Alicia Ines Torres, Amado Alfredo Quintar, Cristina Alicia Maldonado. Endocrinology 2018
13
20

First case of fetal goitrous hypothyroidism due to SLC5A5/NIS mutations.
Athanasia Stoupa, Ghada Al Hage Chehade, Dulanjalee Kariyawasam, Celine Tohier, Christine Bole-Feysot, Patrick Nitschke, Helene Thibault, Marie-Laure Jullie, Michel Polak, Aurore Carré. Eur J Endocrinol 2020
6
20

A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism.
Yui Watanabe, Reham S Ebrhim, Mohamed A Abdullah, Roy E Weiss. Thyroid 2018
13
20

The ERα membrane pool modulates the proliferation of pituitary tumours.
Liliana Del V Sosa, Juan P Petiti, Florencia Picech, Sabrina Chumpen, Juan P Nicola, Pablo Perez, Ana De Paul, Javier Valdez-Taubas, Silvina Gutierrez, Alicia I Torres. J Endocrinol 2019
6
20

Mechanism of anion selectivity and stoichiometry of the Na+/I- symporter (NIS).
Monika Paroder-Belenitsky, Matthew J Maestas, Orsolya Dohán, Juan Pablo Nicola, Andrea Reyna-Neyra, Antonia Follenzi, Ekaterina Dadachova, Sepehr Eskandari, L Mario Amzel, Nancy Carrasco. Proc Natl Acad Sci U S A 2011
42
20

An extremely high dietary iodide supply forestalls severe hypothyroidism in Na+/I- symporter (NIS) knockout mice.
Giuseppe Ferrandino, Rachel R Kaspari, Andrea Reyna-Neyra, Nabil E Boutagy, Albert J Sinusas, Nancy Carrasco. Sci Rep 2017
21
20

Prediction and assessment of splicing alterations: implications for clinical testing.
Amanda B Spurdle, Fergus J Couch, Frans B L Hogervorst, Paolo Radice, Olga M Sinilnikova. Hum Mutat 2008
95
20

The mechanism of sodium and substrate release from the binding pocket of vSGLT.
Akira Watanabe, Seungho Choe, Vincent Chaptal, John M Rosenberg, Ernest M Wright, Michael Grabe, Jeff Abramson. Nature 2010
145
20

Effects of 2-iodohexadecanal in the physiology of thyroid cells.
Luciano E Rossich, Lisa Thomasz, Juan P Nicola, Magali Nazar, Leonardo A Salvarredi, Mario Pisarev, Ana M Masini-Repiso, Christiane Christophe-Hobertus, Daniel Christophe, Guillermo J Juvenal. Mol Cell Endocrinol 2016
13
20

The mammary gland iodide transporter is expressed during lactation and in breast cancer.
U H Tazebay, I L Wapnir, O Levy, O Dohan, L S Zuckier, Q H Zhao, H F Deng, P S Amenta, S Fineberg, R G Pestell,[...]. Nat Med 2000
371
20

A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism.
T Ieiri, P Cochaux, H M Targovnik, M Suzuki, S Shimoda, J Perret, G Vassart. J Clin Invest 1991
126
20

Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting.
J Calado, J Loeffler, O Sakallioglu, F Gok, K Lhotta, J Barata, J Rueff. Kidney Int 2006
64
20

Congenital Hypothyroidism Due to Truncating PAX8 Mutations: A Case Series and Molecular Function Studies.
Megumi Iwahashi-Odano, Keisuke Nagasaki, Maki Fukami, Junko Nishioka, Shuichi Yatsuga, Yumi Asakura, Masanori Adachi, Koji Muroya, Tomonobu Hasegawa, Satoshi Narumi. J Clin Endocrinol Metab 2020
2
50

Dietary I(-) absorption: expression and regulation of the Na(+)/I(-) symporter in the intestine.
Juan Pablo Nicola, Nancy Carrasco, Ana María Masini-Repiso. Vitam Horm 2015
14
20

The paradoxical lean phenotype of hypothyroid mice is marked by increased adaptive thermogenesis in the skeletal muscle.
Rachel R Kaspari, Andrea Reyna-Neyra, Lara Jung, Alejandra Paola Torres-Manzo, Sandro M Hirabara, Nancy Carrasco. Proc Natl Acad Sci U S A 2020
11
20


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.