A citation-based method for searching scientific literature

Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green, Orah S Platt, Douglas M Ruderfer, Christopher A Walsh, David Altshuler, Aravinda Chakravarti, Rudolph E Tanzi, Kari Stefansson, Susan L Santangelo, James F Gusella, Pamela Sklar, Bai-Lin Wu, Mark J Daly. N Engl J Med 2008
Times Cited: 1079



R G Walters, S Jacquemont, A Valsesia, A J de Smith, D Martinet, J Andersson, M Falchi, F Chen, J Andrieux, S Lobbens, B Delobel, F Stutzmann, J S El-Sayed Moustafa, J-C Chèvre, C Lecoeur, V Vatin, S Bouquillon, J L Buxton, O Boute, M Holder-Espinasse, J-M Cuisset, M-P Lemaitre, A-E Ambresin, A Brioschi, M Gaillard, V Giusti, F Fellmann, A Ferrarini, N Hadjikhani, D Campion, A Guilmatre, A Goldenberg, N Calmels, J-L Mandel, C Le Caignec, A David, B Isidor, M-P Cordier, S Dupuis-Girod, A Labalme, D Sanlaville, M Béri-Dexheimer, P Jonveaux, B Leheup, K Ounap, E G Bochukova, E Henning, J Keogh, R J Ellis, K D Macdermot, M M van Haelst, C Vincent-Delorme, G Plessis, R Touraine, A Philippe, V Malan, M Mathieu-Dramard, J Chiesa, B Blaumeiser, R F Kooy, R Caiazzo, M Pigeyre, B Balkau, R Sladek, S Bergmann, V Mooser, D Waterworth, A Reymond, P Vollenweider, G Waeber, A Kurg, P Palta, T Esko, A Metspalu, M Nelis, P Elliott, A-L Hartikainen, M I McCarthy, L Peltonen, L Carlsson, P Jacobson, L Sjöström, N Huang, M E Hurles, S O'Rahilly, I S Farooqi, K Männik, M-R Jarvelin, F Pattou, D Meyre, A J Walley, L J M Coin, A I F Blakemore, P Froguel, J S Beckmann. Nature 2010
Times Cited: 315




List of shared articles



Times cited

Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.
Devanand S Manoli, Matthew W State. Am J Psychiatry 2021
4

Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models.
Sandra Martin Lorenzo, Valérie Nalesso, Claire Chevalier, Marie-Christine Birling, Yann Herault. Mol Autism 2021
2

Dissecting the complexity of CNV pathogenicity: insights from Drosophila and zebrafish models.
Tanzeen Yusuff, Georgios Kellaris, Santhosh Girirajan, Nicholas Katsanis. Curr Opin Genet Dev 2021
0

Copy Number Variations Analysis Identifies QPRT as a Candidate Gene Associated With Susceptibility for Solitary Functioning Kidney.
Xiao Y Zhou, Hao Y Zheng, Li Han, Yan Wang, Li Zhang, Xiao M Shu, Mu L Zhang, Guan N Liu, Lian S Ding. Front Genet 2021
0

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice.
Xiaojun Ren, Nan Yang, Nan Wu, Ximing Xu, Weisheng Chen, Ling Zhang, Yingping Li, Ren-Qian Du, Shuangshuang Dong, Sen Zhao,[...]. J Med Genet 2020
8

Phenotypes Associated with 16p11.2 Copy Number Gains and Losses at a Single Institution.
Caleb Chu, Haotian Wu, Fangling Xu, Joseph W Ray, Allison Britt, Sally S Robinson, Pamela J Lupo, Christine R C Murphy, Charles F Dreyer, Phillip D K Lee,[...]. Lab Med 2020
0

Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children.
Rana Fetit, David J Price, Stephen M Lawrie, Mandy Johnstone. Psychiatr Genet 2020
1

16p11.2 microdeletion imparts transcriptional alterations in human iPSC-derived models of early neural development.
Julien G Roth, Kristin L Muench, Aditya Asokan, Victoria M Mallett, Hui Gai, Yogendra Verma, Stephen Weber, Carol Charlton, Jonas L Fowler, Kyle M Loh,[...]. Elife 2020
3


Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature.
Anna Lengyel, Éva Pinti, Henriett Pikó, Eszter Jávorszky, Dezső David, Mariann Tihanyi, Éva Gönczi, Eszter Kiss, Zsuzsa Tóth, Kálmán Tory,[...]. Eur J Med Genet 2020
0

16p11.2 Copy Number Variations and Neurodevelopmental Disorders.
Benjamin Rein, Zhen Yan. Trends Neurosci 2020
4

Clinical, molecular genetics and therapeutic aspects of syndromic obesity.
E Geets, M E C Meuwissen, W Van Hul. Clin Genet 2019
12