A citation-based method for searching scientific literature

Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi, Joseph Shen, Sung-Hae L Kang, Amber Pursley, Timothy Lotze, Gail Kennedy, Susan Lansky-Shafer, Christine Weaver, Elizabeth R Roeder, Theresa A Grebe, Georgianne L Arnold, Terry Hutchison, Tyler Reimschisel, Stephen Amato, Michael T Geragthy, Jeffrey W Innis, Ewa Obersztyn, Beata Nowakowska, Sally S Rosengren, Patricia I Bader, Dorothy K Grange, Sayed Naqvi, Adolfo D Garnica, Saunder M Bernes, Chin-To Fong, Anne Summers, W David Walters, James R Lupski, Pawel Stankiewicz, Sau Wai Cheung, Ankita Patel. Nat Genet 2008
Times Cited: 385



Raphael Bernier, Kyle J Steinman, Beau Reilly, Arianne Stevens Wallace, Elliott H Sherr, Nicholas Pojman, Heather C Mefford, Jennifer Gerdts, Rachel Earl, Ellen Hanson, Robin P Goin-Kochel, Leandra Berry, Stephen Kanne, LeeAnne Green Snyder, Sarah Spence, Melissa B Ramocki, David W Evans, John E Spiro, Christa L Martin, David H Ledbetter, Wendy K Chung. Genet Med 2016
Times Cited: 73




List of shared articles



Times cited

Clinical evaluation of patients with a neuropsychiatric risk copy number variant.
Samuel Jra Chawner, Cameron J Watson, Michael J Owen. Curr Opin Genet Dev 2021
0

The psychiatric phenotypes of 1q21 distal deletion and duplication.
Stefanie C Linden, Cameron J Watson, Jacqueline Smith, Samuel J R A Chawner, Thomas M Lancaster, Ffion Evans, Nigel Williams, David Skuse, F Lucy Raymond, Jeremy Hall,[...]. Transl Psychiatry 2021
1

Clinical characterization of individuals with the distal 1q21.1 microdeletion.
Stacey D Edwards, Katharina V Schulze, Jill A Rosenfeld, Lauren E Westerfield, Amanda Gerard, Bo Yuan, Elena L Grigorenko, Jennifer E Posey, Weimin Bi, Pengfei Liu. Am J Med Genet A 2021
0

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E Villalon-Reina, Ingrid Agartz, Katrin Amunts, Celso Arango, Nicola J Armstrong,[...]. Hum Brain Mapp 2021
0

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
Ida E Sønderby, Dennis van der Meer, Clara Moreau, Tobias Kaufmann, G Bragi Walters, Maria Ellegaard, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson,[...]. Transl Psychiatry 2021
1


Rare copy number variants in individuals at clinical high risk for psychosis: Enrichment of synaptic/brain-related functional pathways.
Vinita Jagannath, Edna Grünblatt, Anastasia Theodoridou, Beatrice Oneda, Alexander Roth, Miriam Gerstenberg, Maurizia Franscini, Nina Traber-Walker, Christoph U Correll, Karsten Heekeren,[...]. Am J Med Genet B Neuropsychiatr Genet 2020
0

Separable neural mechanisms for the pleiotropic association of copy number variants with neuropsychiatric traits.
Jonathan R Reinwald, Alexander Sartorius, Wolfgang Weber-Fahr, Markus Sack, Robert Becker, Michael Didriksen, Tine B Stensbøl, Adam J Schwarz, Andreas Meyer-Lindenberg, Natalia Gass. Transl Psychiatry 2020
3

Evolution of Human Brain Size-Associated NOTCH2NL Genes Proceeds toward Reduced Protein Levels.
Gerrald A Lodewijk, Diana P Fernandes, Iraklis Vretzakis, Jeanne E Savage, Frank M J Jacobs. Mol Biol Evol 2020
2

Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir,[...]. Prenat Diagn 2020
1

Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literature.
Priyanka Upadhyai, Eram Fatima Amiri, Vishal Singh Guleria, Stephanie L Bielas, Katta Mohan Girisha, Anju Shukla. Clin Dysmorphol 2020
1

Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1.
Hui Pang, Xiaowei Yu, Young Mi Kim, Xianfu Wang, Jeremy K Jinkins, Jianing Yin, Shibo Li, Hongcang Gu. Front Genet 2020
1

Full function of exon junction complex factor, Rbm8a, is critical for interneuron development.
Colleen McSweeney, Fengping Dong, Miranda Chen, Jessica Vitale, Li Xu, Nicole Crowley, Bernhard Luscher, Donghua Zou, Yingwei Mao. Transl Psychiatry 2020
1

Pan-european landscape of research into neurodevelopmental copy number variants: A survey by the MINDDS consortium.
Samuel J R A Chawner, Marina Mihaljevic, Sinead Morrison, Hale Yapici Eser, Anne M Maillard, Beata Nowakowska, Marianne B M van den Bree, Ann Swillen. Eur J Med Genet 2020
0

Brain Disorders and Chemical Pollutants: A Gap Junction Link?
Marc Mesnil, Norah Defamie, Christian Naus, Denis Sarrouilhe. Biomolecules 2020
1

New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies.
Fabiola Ceroni, Domingo Aguilera-Garcia, Nicolas Chassaing, Dorine Arjanne Bax, Fiona Blanco-Kelly, Patricia Ramos, Maria Tarilonte, Cristina Villaverde, Luciana Rodrigues Jacy da Silva, Maria Juliana Ballesta-Martínez,[...]. Hum Genet 2019
18

An eight-case 1q21 region series: novel aberrations and clinical variability with new features.
A C Ceylan, I Sahin, H B Erdem, G Kayhan, P O Simsek-Kiper, G E Utine, F Percin, K Boduroglu, M Alikasifoglu. J Intellect Disabil Res 2019
2


1q21.1 Deletions and Duplications in 2 Siblings with Psychiatric Problems.
Hande Kaymakçalan, Peining Li. Indian J Pediatr 2019
0

Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound.
Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang, Chen-Chi Lee. Taiwan J Obstet Gynecol 2019
2

1q21.1 Duplication syndrome and epilepsy: Case report and review.
Ioulia Gourari, Romaine Schubert, Aparna Prasad. Neurol Genet 2018
4


Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis.
Ian T Fiddes, Gerrald A Lodewijk, Meghan Mooring, Colleen M Bosworth, Adam D Ewing, Gary L Mantalas, Adam M Novak, Anouk van den Bout, Alex Bishara, Jimi L Rosenkrantz,[...]. Cell 2018
143

Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.
Antonio Benítez-Burraco, Montserrat Barcos-Martínez, Isabel Espejo-Portero, Maite Fernández-Urquiza, Raúl Torres-Ruiz, Sandra Rodríguez-Perales, Ma Salud Jiménez-Romero. Front Pediatr 2018
5

1q21.1 microduplication: large verbal-nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number.
Jean Xavier, Bo Zhou, Frédéric Bilan, Xianglong Zhang, Brigitte Gilbert-Dussardier, Sylvie Viaux-Savelon, Reenal Pattni, Steve S Ho, David Cohen, Douglas F Levinson,[...]. NPJ Genom Med 2018
3

Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies.
Xiuqing Ji, Qiong Pan, Yan Wang, Yun Wu, Jing Zhou, An Liu, Fengchang Qiao, Dingyuan Ma, Ping Hu, Zhengfeng Xu. Front Genet 2018
2

22q and two: 22q11.2 deletion syndrome and coexisting conditions.
Jennifer L Cohen, Terrence B Crowley, Daniel E McGinn, Carey McDougall, Marta Unolt, Michele P Lambert, Beverly S Emanuel, Elaine H Zackai, Donna M McDonald-McGinn. Am J Med Genet A 2018
6

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen,[...]. Taiwan J Obstet Gynecol 2018
3

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.
Mary Ella Pierpont, Martina Brueckner, Wendy K Chung, Vidu Garg, Ronald V Lacro, Amy L McGuire, Seema Mital, James R Priest, William T Pu, Amy Roberts,[...]. Circulation 2018
87

Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
Hong-Dan Wang, Lin Liu, Dong Wu, Tao Li, Cun-Ying Cui, Lian-Zhong Zhang, Cheng-Zeng Wang. J Gene Med 2017
9

The birth of a human-specific neural gene by incomplete duplication and gene fusion.
Max L Dougherty, Xander Nuttle, Osnat Penn, Bradley J Nelson, John Huddleston, Carl Baker, Lana Harshman, Michael H Duyzend, Mario Ventura, Francesca Antonacci,[...]. Genome Biol 2017
19

Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy.
Cyrille Robert, Laurent Pasquier, David Cohen, Mélanie Fradin, Roberto Canitano, Léna Damaj, Sylvie Odent, Sylvie Tordjman. Int J Mol Sci 2017
11