A citation-based method for searching scientific literature

Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H Zackai, Paige Kaplan, Jaya Ganesh, Ian D Krantz, Nancy B Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B Lakshmi, Anthony Leotta, Jude Kendall, Yoon-Ha Lee, Vladimir Vacic, Sydney Gary, Lilia M Iakoucheva, Timothy J Crow, Susan L Christian, Jeffrey A Lieberman, T Scott Stroup, Terho Lehtimäki, Kaija Puura, Chad Haldeman-Englert, Justin Pearl, Meredith Goodell, Virginia L Willour, Pamela Derosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J McMahon, Anil K Malhotra, James B Potash, Thomas G Schulze, Markus M Nöthen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara M Lajonchere, James S Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R Mendell, Nick Craddock, Michael J Owen, Michael C O'Donovan, Tamim H Shaikh, Ezra Susser, Lynn E Delisi, Patrick F Sullivan, Curtis K Deutsch, Judith Rapoport, Deborah L Levy, Mary-Claire King, Jonathan Sebat. Nat Genet 2009
Times Cited: 475



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

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

The Role of Genetic Variation of BMI, Body Composition, and Fat Distribution for Mental Traits and Disorders: A Look-Up and Mendelian Randomization Study.
Triinu Peters, Lena Nüllig, Jochen Antel, Roaa Naaresh, Björn-Hergen Laabs, Lisa Tegeler, Chaima Amhaouach, Lars Libuda, Anke Hinney, Johannes Hebebrand. Front Genet 2020
3

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

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

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

The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability.
Fátima Gimeno-Ferrer, David Albuquerque, Carola Guzmán Luján, Goitzane Marcaida Benito, Cristina Torreira Banzas, Alfredo Repáraz-Andrade, Virginia Ballesteros Cogollos, Montserrat Aleu Pérez-Gramunt, Enrique Galán Gómez, Inés Quintela,[...]. J Hum Genet 2019
1

Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions.
Thomas Arbogast, Parisa Razaz, Jacob Ellegood, Spencer U McKinstry, Serkan Erdin, Benjamin Currall, Tanya Aneichyk, Jason P Lerch, Lily R Qiu, Ramona M Rodriguiz,[...]. Hum Mol Genet 2019
11

KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders.
Xinchen Teng, Abdel Aouacheria, Loïc Lionnard, Kyle A Metz, Lucian Soane, Atsushi Kamiya, J Marie Hardwick. CNS Neurosci Ther 2019
16

The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
Giuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, Gilles Willemin, Katherine M Munson, Xander Nuttle, Rachel Earl, Jacqueline Chrast, Kendra Hoekzema, Davide Risso,[...]. Am J Hum Genet 2019
6

Chemogenetic Activation of Prefrontal Cortex Rescues Synaptic and Behavioral Deficits in a Mouse Model of 16p11.2 Deletion Syndrome.
Wei Wang, Benjamin Rein, Freddy Zhang, Tao Tan, Ping Zhong, Luye Qin, Zhen Yan. J Neurosci 2018
22