A citation-based method for searching scientific literature

Kate Baker, Jacob A S Vorstman. Curr Opin Neurol 2012
Times Cited: 46



Jacob A S Vorstman, Elemi J Breetvelt, Sasja N Duijff, Stephan Eliez, Maude Schneider, Maria Jalbrzikowski, Marco Armando, Stefano Vicari, Vandana Shashi, Stephen R Hooper, Eva W C Chow, Wai Lun Alan Fung, Nancy J Butcher, Donald A Young, Donna M McDonald-McGinn, Annick Vogels, Therese van Amelsvoort, Doron Gothelf, Ronnie Weinberger, Abraham Weizman, Petra W J Klaassen, Sanne Koops, Wendy R Kates, Kevin M Antshel, Tony J Simon, Opal Y Ousley, Ann Swillen, Raquel E Gur, Carrie E Bearden, RenĂ© S Kahn, Anne S Bassett. JAMA Psychiatry 2015
Times Cited: 126




List of shared articles



Times cited

Assessing auditory processing endophenotypes associated with Schizophrenia in individuals with 22q11.2 deletion syndrome.
Ana A Francisco, John J Foxe, Douwe J Horsthuis, Danielle DeMaio, Sophie Molholm. Transl Psychiatry 2020
7

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
455

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology.
Sinead Morrison, Samuel J R A Chawner, Therese A M J van Amelsvoort, Ann Swillen, Claudia Vingerhoets, Elfi Vergaelen, David E J Linden, Stefanie Linden, Michael J Owen, Marianne B M van den Bree. Transl Psychiatry 2020
10

The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome.
Samuel J R A Chawner, Maria Niarchou, Joanne L Doherty, Hayley Moss, Michael J Owen, Marianne B M van den Bree. J Psychiatr Res 2019
7

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome.
Ania M Fiksinski, Maude Schneider, Janneke Zinkstok, Danielle Baribeau, Samuel J R A Chawner, Jacob A S Vorstman. Curr Psychiatry Rep 2021
5

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
2


Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.
Ania M Fiksinski, Maude Schneider, Clodagh M Murphy, Marco Armando, Stefano Vicari, Jaume M Canyelles, Doron Gothelf, Stephan Eliez, Elemi J Breetvelt, Celso Arango,[...]. Am J Med Genet A 2018
31

Developmental trajectories in 22q11.2 deletion.
Ann Swillen, Donna McDonald-McGinn. Am J Med Genet C Semin Med Genet 2015
88