A citation-based method for searching scientific literature

Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino, Marjan M Nezarati, Alexander Asamoah, Kelly E Jackson, Gordon C Gowans, Judith A Martin, Erin P Carmany, David W Stockton, Rhonda E Schnur, Lynette S Penney, Donna M Martin, Salmo Raskin, Kathleen Leppig, Heidi Thiese, Rosemarie Smith, Erika Aberg, Dmitriy M Niyazov, Luis F Escobar, Dima El-Khechen, Kisha D Johnson, Robert R Lebel, Kiana Siefkas, Susie Ball, Natasha Shur, Marianne McGuire, Campbell K Brasington, J Edward Spence, Laura S Martin, Carol Clericuzio, Blake C Ballif, Lisa G Shaffer, Evan E Eichler. N Engl J Med 2012
Times Cited: 353



Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson, Christopher E Mason, Kaya Bilguvar, Patricia B S Celestino-Soper, Murim Choi, Emily L Crawford, Lea Davis, Nicole R Davis Wright, Rahul M Dhodapkar, Michael DiCola, Nicholas M DiLullo, Thomas V Fernandez, Vikram Fielding-Singh, Daniel O Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald S Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K Lowe, Sabata C Lund, Anna D McGrew, Kyle A Meyer, William J Moffat, John D Murdoch, Brian J O'Roak, Gordon T Ober, Rebecca S Pottenger, Melanie J Raubeson, Youeun Song, Qi Wang, Brian L Yaspan, Timothy W Yu, Ilana R Yurkiewicz, Arthur L Beaudet, Rita M Cantor, Martin Curland, Dorothy E Grice, Murat Günel, Richard P Lifton, Shrikant M Mane, Donna M Martin, Chad A Shaw, Michael Sheldon, Jay A Tischfield, Christopher A Walsh, Eric M Morrow, David H Ledbetter, Eric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I Brooks, James S Sutcliffe, Edwin H Cook, Daniel Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W State. Neuron 2011
Times Cited: 802




List of shared articles



Times cited

A report on seven fetal cases associated with 15q11-q13 microdeletion and microduplication.
Xiuzhu Huang, Jieping Chen, Wenlong Hu, Lu Li, Huiyan He, Hui Guo, Qiuyan Liao, Mei Ye, Donge Tang, Yong Dai. Mol Genet Genomic Med 2021
0


Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Amy B Wilfert, Tychele N Turner, Shwetha C Murali, PingHsun Hsieh, Arvis Sulovari, Tianyun Wang, Bradley P Coe, Hui Guo, Kendra Hoekzema, Trygve E Bakken,[...]. Nat Genet 2021
0

Developmental disabilities across the world: A scientometric review from 1936 to 2020.
Alessandro Carollo, Andrea Bonassi, Mengyu Lim, Giulio Gabrieli, Peipei Setoh, Dagmara Dimitriou, Vahid Aryadoust, Gianluca Esposito. Res Dev Disabil 2021
1


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

Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder.
Klaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, R Sean Hill, Maria H Chahrour, Bhaven K Mehta, Sarah Servattalab, Bulent Ataman, Anh-Thu N Lam, Eric M Morrow,[...]. Sci Rep 2020
0

Evaluation of Chromosome Microarray Analysis in a Large Cohort of Females with Autism Spectrum Disorders: A Single Center Italian Study.
Sara Calderoni, Ivana Ricca, Giulia Balboni, Romina Cagiano, Denise Cassandrini, Stefano Doccini, Angela Cosenza, Deborah Tolomeo, Raffaella Tancredi, Filippo Maria Santorelli,[...]. J Pers Med 2020
0

Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature.
Natália Oliva-Teles, Maria Chiara de Stefano, Louise Gallagher, Severin Rakic, Paula Jorge, Goran Cuturilo, Silvana Markovska-Simoska, Isabella Borg, Jeanne Wolstencroft, Zeynep Tümer,[...]. Int J Environ Res Public Health 2020
0

Genetics and epigenetics of autism spectrum disorder-current evidence in the field.
Barbara Wiśniowiecka-Kowalnik, Beata Anna Nowakowska. J Appl Genet 2019
46

Refining the Phenotype of Recurrent Rearrangements of Chromosome 16.
Serena Redaelli, Silvia Maitz, Francesca Crosti, Elena Sala, Nicoletta Villa, Luigina Spaccini, Angelo Selicorni, Miriam Rigoldi, Donatella Conconi, Leda Dalprà,[...]. Int J Mol Sci 2019
13

Genetic basis of human congenital anomalies of the kidney and urinary tract.
Simone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, Ali G Gharavi. J Clin Invest 2018
33