A citation-based method for searching scientific literature

Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger, Regina Reissmann, Irene Sudholt, Christian T Thiel, Arif B Ekici, André Reis, Emilia K Bijlsma, Joris Andrieux, Anne Dieux, David FitzPatrick, Susanne Ritter, Alessandra Baumer, Beatrice Latal, Barbara Plecko, Oskar G Jenni, Anita Rauch. J Med Genet 2014
Times Cited: 57



Gea Beunders, Els Voorhoeve, Christelle Golzio, Luba M Pardo, Jill A Rosenfeld, Michael E Talkowski, Ingrid Simonic, Anath C Lionel, Sarah Vergult, Robert E Pyatt, Jiddeke van de Kamp, Aggie Nieuwint, Marjan M Weiss, Patrizia Rizzu, Lucilla E N I Verwer, Rosalina M L van Spaendonk, Yiping Shen, Bai-lin Wu, Tingting Yu, Yongguo Yu, Colby Chiang, James F Gusella, Amelia M Lindgren, Cynthia C Morton, Ellen van Binsbergen, Saskia Bulk, Els van Rossem, Olivier Vanakker, Ruth Armstrong, Soo-Mi Park, Lynn Greenhalgh, Una Maye, Nicholas J Neill, Kristin M Abbott, Susan Sell, Roger Ladda, Darren M Farber, Patricia I Bader, Tom Cushing, Joanne M Drautz, Laura Konczal, Patricia Nash, Emily de Los Reyes, Melissa T Carter, Elizabeth Hopkins, Christian R Marshall, Lucy R Osborne, Karen W Gripp, Devon Lamb Thrush, Sayaka Hashimoto, Julie M Gastier-Foster, Caroline Astbury, Bauke Ylstra, Hanne Meijers-Heijboer, Danielle Posthuma, Björn Menten, Geert Mortier, Stephen W Scherer, Evan E Eichler, Santhosh Girirajan, Nicholas Katsanis, Alexander J Groffen, Erik A Sistermans. Am J Hum Genet 2013
Times Cited: 95




List of shared articles



Times cited

Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review.
Christophe Gauld, Alice Poisson, Julie Reversat, Elodie Peyroux, Françoise Houdayer-Robert, Massimiliano Rossi, Gaetan Lesca, Damien Sanlaville, Caroline Demily. BMC Psychiatry 2021
0

Regulation of neuronal migration, an emerging topic in autism spectrum disorders.
Orly Reiner, Eyal Karzbrun, Aditya Kshirsagar, Kozo Kaibuchi. J Neurochem 2016
60

Germ cell mosaicism for AUTS2 exon 6 deletion.
Laura Gieldon, Anna Jauch, Katharina Obeid, Lilian Kaufmann, Katrin Hinderhofer, Ulrich Haug, Ute Moog. Am J Med Genet A 2021
1

Attention Deficit Hyperactivity and Autism Spectrum Disorders as the Core Symptoms of AUTS2 Syndrome: Description of Five New Patients and Update of the Frequency of Manifestations and Genotype-Phenotype Correlation.
Carolina Sanchez-Jimeno, Fiona Blanco-Kelly, Fermina López-Grondona, Rebeca Losada-Del Pozo, Beatriz Moreno, María Rodrigo-Moreno, Elena Martinez-Cayuelas, Rosa Riveiro-Alvarez, María Fenollar-Cortés, Carmen Ayuso,[...]. Genes (Basel) 2021
0

Exonic deletions of AUTS2 in Chinese patients with developmental delay and intellectual disability.
Yanjie Fan, Wenjuan Qiu, Lili Wang, Xuefan Gu, Yongguo Yu. Am J Med Genet A 2016
8

A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.
Gea Beunders, Jiddeke van de Kamp, Pradeep Vasudevan, Jenny Morton, Katrien Smets, Tjitske Kleefstra, Sonja A de Munnik, Janneke Schuurs-Hoeijmakers, Berten Ceulemans, Marcella Zollino,[...]. J Med Genet 2016
22