A citation-based method for searching scientific literature

Stephen J Marx, David Goltzman. J Bone Miner Res 2019
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
Bin Guan, James M Welch, Julie C Sapp, Hua Ling, Yulong Li, Jennifer J Johnston, Electron Kebebew, Leslie G Biesecker, William F Simonds, Stephen J Marx,[...]. Am J Hum Genet 2016
64
37

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.
J D Carpten, C M Robbins, A Villablanca, L Forsberg, S Presciuttini, J Bailey-Wilson, W F Simonds, E M Gillanders, A M Kennedy, J D Chen,[...]. Nat Genet 2002
473
37

Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotype.
Markus Glaudo, Saskia Letz, Marcus Quinkler, Ulrich Bogner, Ulf Elbelt, Christian J Strasburger, Dirk Schnabel, Erwin Lankes, Sandra Scheel, Joachim Feldkamp,[...]. Eur J Endocrinol 2016
20
31

Familial hypocalciuric hypercalcemia and related disorders.
Janet Y Lee, Dolores M Shoback. Best Pract Res Clin Endocrinol Metab 2018
47
31


Analysis of Activating GCM2 Sequence Variants in Sporadic Parathyroid Adenomas.
Aaliyah Riccardi, Tori Aspir, Lilia Shen, Chia-Ling Kuo, Taylor C Brown, Reju Korah, Timothy D Murtha, Justin Bellizzi, Kourosh Parham, Tobias Carling,[...]. J Clin Endocrinol Metab 2019
17
25

Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma.
Luís Cardoso, Mark Stevenson, Rajesh V Thakker. Hum Mutat 2017
51
25

The American Association of Endocrine Surgeons Guidelines for Definitive Management of Primary Hyperparathyroidism.
Scott M Wilhelm, Tracy S Wang, Daniel T Ruan, James A Lee, Sylvia L Asa, Quan-Yang Duh, Gerard M Doherty, Miguel F Herrera, Janice L Pasieka, Nancy D Perrier,[...]. JAMA Surg 2016
490
25

Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).
Rajesh V Thakker, Paul J Newey, Gerard V Walls, John Bilezikian, Henning Dralle, Peter R Ebeling, Shlomo Melmed, Akihiro Sakurai, Francesco Tonelli, Maria Luisa Brandi. J Clin Endocrinol Metab 2012
683
18

Cloning and characterization of an extracellular Ca(2+)-sensing receptor from bovine parathyroid.
E M Brown, G Gamba, D Riccardi, M Lombardi, R Butters, O Kifor, A Sun, M A Hediger, J Lytton, S C Hebert. Nature 1993
18


CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism.
Karin van der Tuin, Carli M J Tops, Muriel A Adank, Jan-Maarten Cobben, Neveen A T Hamdy, Marjolijn C Jongmans, Fred H Menko, Bernadette P M van Nesselrooij, Romana T Netea-Maier, Jan C Oosterwijk,[...]. J Clin Endocrinol Metab 2017
39
18

Parafibromin-deficient (HPT-JT Type, CDC73 Mutated) Parathyroid Tumors Demonstrate Distinctive Morphologic Features.
Anthony J Gill, Grace Lim, Veronica K Y Cheung, Juliana Andrici, Joanna L Perry-Keene, Julie Paik, Loretta Sioson, Adele Clarkson, Amy Sheen, Catherine Luxford,[...]. Am J Surg Pathol 2019
43
18

Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure.
Mustapha El Lakis, Pavel Nockel, Bin Guan, Sunita Agarwal, James Welch, William F Simonds, Stephen Marx, Yulong Li, Naris Nilubol, Dhaval Patel,[...]. Surgery 2018
15
20

Neonatal severe hyperparathyroidism caused by homozygous mutation in CASR: A rare cause of life-threatening hypercalcemia.
Heidi Murphy, Jessica Patrick, Eileen Báez-Irizarry, Yves Lacassie, Ricardo Gómez, Alfonso Vargas, Brian Barkemeyer, Sohit Kanotra, Regina M Zambrano. Eur J Med Genet 2016
18
18


Neonatal hyperparathyroidism with a heterozygous calcium-sensing receptor (CASR) R185Q mutation: clinical benefit from cinacalcet.
Christina M S Reh, Geoffrey N Hendy, David E C Cole, Debra D Jeandron. J Clin Endocrinol Metab 2011
62
18

Familial hypocalciuric hypercalcaemia: a review.
Signe E Christensen, Peter H Nissen, Peter Vestergaard, Leif Mosekilde. Curr Opin Endocrinol Diabetes Obes 2011
70
18


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
18

Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors.
Filomena Cetani, Elena Pardi, Simona Borsari, Paolo Viacava, Giada Dipollina, Luisella Cianferotti, Elena Ambrogini, Elisabetta Gazzerro, Giacomo Colussi, Piero Berti,[...]. J Clin Endocrinol Metab 2004
162
18

Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma.
Trisha M Shattuck, Stiina Välimäki, Takao Obara, Randall D Gaz, Orlo H Clark, Dolores Shoback, Margaret E Wierman, Katsuyoshi Tojo, Christiane M Robbins, John D Carpten,[...]. N Engl J Med 2003
364
18

Multiple Endocrine Neoplasia Type 1 (MEN1): An Update and the Significance of Early Genetic and Clinical Diagnosis.
Crystal D C Kamilaris, Constantine A Stratakis. Front Endocrinol (Lausanne) 2019
63
18

The clinical importance of parathyroid atypia: is long-term surveillance necessary?
Kelly L McCoy, Raja R Seethala, Michaele J Armstrong, Marina N Nikiforova, Michael T Stang, Sally E Carty, Linwah Yip. Surgery 2015
18
18

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.
M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, Anita A C Reed, Treena Cranston, Clare E Thakker, Lorna Gregory, Andrew J Rimmer, Nigel Rust, Una Graham,[...]. Nat Genet 2013
159
18

Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia.
M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, Valerie N Babinsky, Rosie A Head, Treena Cranston, Nigel Rust, Maurine R Hobbs, Hunter Heath, Rajesh V Thakker. N Engl J Med 2013
212
18


Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.
M R Pollak, E M Brown, Y H Chou, S C Hebert, S J Marx, B Steinmann, T Levi, C E Seidman, J G Seidman. Cell 1993
775
18

Atypical parathyroid adenomas: challenging lesions in the differential diagnosis of endocrine tumors.
Filomena Cetani, Claudio Marcocci, Liborio Torregrossa, Elena Pardi. Endocr Relat Cancer 2019
44
18



Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome.
K J Bradley, M R Hobbs, I D Buley, J D Carpten, B M Cavaco, J E Fares, P Laidler, S Manek, C M Robbins, I S Salti,[...]. J Intern Med 2005
101
12

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)
D Trump, B Farren, C Wooding, J T Pang, G M Besser, K D Buchanan, C R Edwards, D A Heath, C E Jackson, S Jansen,[...]. QJM 1996
338
12

Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the Fourth International Workshop.
Richard Eastell, Maria Luisa Brandi, Aline G Costa, Pierre D'Amour, Dolores M Shoback, Rajesh V Thakker. J Clin Endocrinol Metab 2014
190
12

Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism.
Bin Guan, James M Welch, Meghana Vemulapalli, Yulong Li, Hua Ling, Electron Kebebew, William F Simonds, Stephen J Marx, Sunita K Agarwal. J Endocr Soc 2017
16
12

Weight of normal parathyroid glands in patients with parathyroid adenomas.
Kathy Yao, Frederick R Singer, Sanford I Roth, Aaron Sassoon, Cynthia Ye, Armando E Giuliano. J Clin Endocrinol Metab 2004
42
12

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families.
B T Teh, F Farnebo, S Twigg, A Höög, S Kytölä, E Korpi-Hyövälti, F K Wong, J Nordenström, L Grimelius, K Sandelin,[...]. J Clin Endocrinol Metab 1998
106
12

Analysis of the GCM2 gene in isolated hypoparathyroidism: a molecular and biochemical study.
Alexander Maret, Changlin Ding, Sara Levine Kornfield, Michael A Levine. J Clin Endocrinol Metab 2008
28
12

TLE6 mutation causes the earliest known human embryonic lethality.
Anas M Alazami, Salma M Awad, Serdar Coskun, Saad Al-Hassan, Hadia Hijazi, Firdous M Abdulwahab, Coralie Poizat, Fowzan S Alkuraya. Genome Biol 2015
111
12

Familial hypocalciuric hypercalcemia: the relation to primary parathyroid hyperplasia.
S J Marx, A M Spiegel, M A Levine, R E Rizzoli, R D Lasker, A C Santora, R W Downs, G D Aurbach. N Engl J Med 1982
94
12

Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor.
T Carling, E Szabo, M Bai, P Ridefelt, G Westin, P Gustavsson, S Trivedi, P Hellman, E M Brown, N Dahl,[...]. J Clin Endocrinol Metab 2000
145
12

Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree.
M Kassem, T A Kruse, F K Wong, C Larsson, B T Teh. J Clin Endocrinol Metab 2000
73
12

Familial hyperparathyroidism without multiple endocrine neoplasia.
S M Huang, Q Y Duh, J Shaver, A E Siperstein, J L Kraimps, O H Clark. World J Surg 1997
47
12

The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds.
S J Marx, M F Attie, M A Levine, A M Spiegel, R W Downs, R D Lasker. Medicine (Baltimore) 1981
307
12

Frequent large germline HRPT2 deletions in a French National cohort of patients with primary hyperparathyroidism.
Léopoldine Bricaire, Marie-Françoise Odou, Catherine Cardot-Bauters, Brigitte Delemer, Marie-Odile North, Sylvie Salenave, Delphine Vezzosi, Jean-Marc Kuhn, Arnaud Murat, Philippe Caron,[...]. J Clin Endocrinol Metab 2013
74
12


A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrations.
D E Cole, V D Peltekova, L A Rubin, G A Hawker, R Vieth, C C Liew, D M Hwang, J Evrovski, G N Hendy. Lancet 1999
135
12



Cinacalcet therapy in an infant with an R185Q calcium-sensing receptor mutation causing hyperparathyroidism: a case report and review of the literature.
Thomas E Forman, Anna-Kaisa Niemi, Priya Prahalad, Run Zhang Shi, Laura M Nally. J Pediatr Endocrinol Metab 2019
10
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.