A citation-based method for searching scientific literature

Sarah Jesse, Jan Philipp Delling, Michael Schön, Tobias M Boeckers, Albert Ludolph, Makbule Senel. Int J Mol Sci 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Skull and vertebral bone marrow are myeloid cell reservoirs for the meninges and CNS parenchyma.
Andrea Cugurra, Tornike Mamuladze, Justin Rustenhoven, Taitea Dykstra, Giorgi Beroshvili, Zev J Greenberg, Wendy Baker, Zach Papadopoulos, Antoine Drieu, Susan Blackburn,[...]. Science 2021
122
50

The Impact of SARS-CoV-2 Infection on the Development of Neurodegeneration in Multiple Sclerosis.
Angela Dziedzic, Joanna Saluk-Bijak, Elzbieta Miller, Marcin Niemcewicz, Michal Bijak. Int J Mol Sci 2021
14
50

Intrathecal Inflammation in Progressive Multiple Sclerosis.
Salvatore Monaco, Richard Nicholas, Richard Reynolds, Roberta Magliozzi. Int J Mol Sci 2020
21
50


MicroRNAs, Multiple Sclerosis, and Depression.
Hsiuying Wang. Int J Mol Sci 2021
6
50

Circadian control of brain glymphatic and lymphatic fluid flow.
Lauren M Hablitz, Virginia Plá, Michael Giannetto, Hanna S Vinitsky, Frederik Filip Stæger, Tanner Metcalfe, Rebecca Nguyen, Abdellatif Benrais, Maiken Nedergaard. Nat Commun 2020
126
50

Contribution of Metabolomics to Multiple Sclerosis Diagnosis, Prognosis and Treatment.
Marianna Gabriella Rispoli, Silvia Valentinuzzi, Giovanna De Luca, Piero Del Boccio, Luca Federici, Maria Di Ioia, Anna Digiovanni, Eleonora Agata Grasso, Valeria Pozzilli, Alessandro Villani,[...]. Int J Mol Sci 2021
1
100

Correction to: A case report of Phelan-McDermid syndrome: preliminary results of the treatment with growth hormone therapy.
Rui Jin Xie, Tian Xiao Li, Chenyu Sun, Ce Cheng, Jinlin Zhao, Hua Xu, Yueying Liu. Ital J Pediatr 2021
3
50

A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes.
Na Xu, Hui Lv, Tingting Yang, Xiujuan Du, Yu Sun, Bing Xiao, Yanjie Fan, Xiaomei Luo, Yongkun Zhan, Lili Wang,[...]. Orphanet J Rare Dis 2020
9
50

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A Ting Wang, Guiqing Cai, Elena Parkhomenko,[...]. Mol Autism 2013
183
50


A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Alexandre Mathieu, Damien Haye, Laurence Perrin, Céline Dupont, Sandrine Passemard,[...]. NPJ Genom Med 2017
32
50

Fraternal twins with Phelan-McDermid syndrome not involving the SHANK3 gene: case report and literature review.
Shan Li, Ke-Wang Xi, Ting Liu, Ying Zhang, Meng Zhang, Li-Dong Zeng, Juan Li. BMC Med Genomics 2020
7
50

Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.
Sara M Sarasua, Luigi Boccuto, Julia L Sharp, Alka Dwivedi, Chin-Fu Chen, Jonathan D Rollins, R Curtis Rogers, Katy Phelan, Barbara R DuPont. Hum Genet 2014
97
50

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).
K Phelan, H E McDermid. Mol Syndromol 2012
271
50

Genotype-phenotype correlation in Phelan-McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes.
Arianna Ricciardello, Pasquale Tomaiuolo, Antonio M Persico. Am J Med Genet A 2021
21
50

Deletion 22q13.3 syndrome.
Mary C Phelan. Orphanet J Rare Dis 2008
139
50

Recent developments in Phelan-McDermid syndrome research: an update on cognitive development, communication and psychiatric disorders.
Annick Vogels, Gilles Droogmans, Elfi Vergaelen, Griet Van Buggenhout, Ann Swillen. Curr Opin Psychiatry 2021
4
50

Diagnosis of metachromatic leukodystrophy in a patient with regression and Phelan-McDermid syndrome.
Hyunji Ahn, Go Hun Seo, Changwon Keum, Sun Hee Heo, Taeho Kim, Jeongmin Choi, Mi-Sun Yum, Beom Hee Lee. Brain Dev 2020
2
50

Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome.
Amanda Brignell, Conway Gu, Alison Holm, Bronwyn Carrigg, Daisy A Sheppard, David J Amor, Angela T Morgan. Eur J Hum Genet 2021
7
50

Fetal gastroschisis associated with monosomy 22 mosaicism and absent cerebral diastolic flow.
R M Lewinsky, J M Johnson, T T Lao, E J Winsor, H Cohen. Prenat Diagn 1990
14
50

Co-occurrence of Metachromatic Leukodystrophy in Phelan-McDermid Syndrome.
Dararat Mingbunjerdsuk, Melissa Wong, Xiuhua Bozarth, Angela Sun. J Child Neurol 2021
2
50

A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case.
Claudia Ismania Samogy-Costa, Elisa Varella-Branco, Frederico Monfardini, Helen Ferraz, Rodrigo Ambrósio Fock, Ricardo Henrique Almeida Barbosa, André Luiz Santos Pessoa, Ana Beatriz Alvarez Perez, Naila Lourenço, Maria Vibranovski,[...]. J Neurodev Disord 2019
14
50

Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome.
Gilles Droogmans, Ann Swillen, Griet Van Buggenhout. Mol Syndromol 2020
12
50

Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.
Silvia De Rubeis, Paige M Siper, Allison Durkin, Jordana Weissman, François Muratet, Danielle Halpern, Maria Del Pilar Trelles, Yitzchak Frank, Reymundo Lozano, A Ting Wang,[...]. Mol Autism 2018
83
50


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.