ResearcherID Thomson Reuters  

Pinto, Dalila
Create a ResearcherID badge for this researcher View publications analytics for this researcher
Close
ResearcherID: C-4218-2016
Other Names: Pinto D.
URL: http://www.researcherid.com/rid/C-4218-2016
Subject: Genetics & Heredity; Neurosciences & Neurology; Psychiatry
ORCID: http://orcid.org/0000-0002-8769-0846
My Institutions (more details)
Primary Institution:
Sub-org/Dept: Psychiatry; Genetics and Genomic Sciences; Mindich Child Health & Development Institute; Seaver Autism Center; Icahn Institute for Genomics and Multiscale Biology; Friedman Brain Institute
Role:
My URLs: https://pintolab.mssm.edu
 
 

This list contains papers that I have authored.

publication(s)  
First Page Previous Page Page   of  8  Go Next Page Last Page
  Sort by:    Results per page: 
1.  Title: Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa.
 Author(s): Duncan, Laramie; Yilmaz, Zeynep; Gaspar, Helena; et al.
 Source: The American journal of psychiatry Pages: appiajp201716121402 Published: 2017-May-12
 DOI: 10.1176/appi.ajp.2017.16121402
added
29-Aug-17
2.  Title: A CTNNA3 compound heterozygous deletion implicates a role for alpha T-catenin in susceptibility to autism spectrum disorder
 Author(s): Bacchelli, Elena; Ceroni, Fabiola; Pinto, Dalila; et al.
 Source: Journal of Neurodevelopmental Disorders Volume: 6 Published: JUL 10 2014
 Times Cited: 9
 DOI: 10.1186/1866-1955-6-17
added
29-Aug-17
3.  Title: Individual common variants exert weak effects on the risk for autism spectrum disorderspi
 Author(s): Anney, Richard; Klei, Lambertus; Pinto, Dalila; et al.
 Source: Human Molecular Genetics Volume: 21 Issue: 21 Pages: 4781-4792 Published: NOV 1 2012
 Times Cited: 149
 DOI: 10.1093/hmg/dds301
added
29-Aug-17
4.  Title: Gene symbol: KCNQ2. Disease: Benign neonatal familial convulsion.
 Author(s): Pinto, D; de Haan, G-J; Carton, D; et al.
 Source: Human genetics Volume: 117 Issue: 2-3 Pages: 300 Published: 2005-Jul
added
29-Aug-17
5.  Title: A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma
 Author(s): Ceroni, F.; Sagar, A.; Simpson, N. H.; et al.
 Times Cited: 14
 DOI: 10.1002/aur.1365
added
29-Aug-17
6.  Title: A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3
 Author(s): Pagnamenta, A. T.; Holt, R.; Yusuf, M.; et al.
 Times Cited: 16
 DOI: 10.1007/s11689-011-9076-5
added
29-Aug-17
7.  Title: A genome-wide association study of anorexia nervosa
 Author(s): Boraska, V.; Franklin, C. S.; Floyd, J. A.; et al.
 Times Cited: 70
 DOI: 10.1038/mp.2013.187
added
29-Aug-17
8.  Title: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
 Author(s): Li, D.; Chang, X.; Connolly, J. J.; et al.
 Times Cited: 1
 DOI: 10.1038/s41598-017-01674-8
added
29-Aug-17
9.  Title: A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus
 Author(s): Oei, L.; Hsu, Y. H.; Styrkarsdottir, U.; et al.
 Times Cited: 19
 DOI: 10.1136/jmedgenet-2013-102064
added
29-Aug-17
10.  Title: A genome-wide linkage and association scan reveals novel loci for autism
 Author(s): Weiss, L. A.; Arking, D. E.; Gene Discovery Project of Johns, Hopkins; et al.
 Times Cited: 340
 DOI: 10.1038/nature08490
added
29-Aug-17
publication(s)  
First Page Previous Page Page   of  8  Go Next Page Last Page
  Sort by:    Results per page: