MonicaBProudMD

PubMed

• 45 citations
  Identification of novel candidate disease genes from de novo exonic copy number variants
  Tomasz Gambin, Bo Yuan, Weimin Bi, Pengfei Liu, Jill A. Rosenfeld, Zeynep Coban-Akdemir, Amber N. Pursley, Sandesh C.S. Nagamani, Ronit Marom, Sailaja Golla, Lauren De...> ;Genome Medicine. 2017 Sep 21
• 51 citations
  The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications
  Madelyn A. Gillentine, Leandra N. Berry, Robin P. Goin-Kochel, May Ali, Jun Ge, Danielle Guffey, Jill A. Rosenfeld, Vickie L. Hannig, Patricia I. Bader, Monica Proud, ...> ;Journal of Autism and Developmental Disorders. 2017 Mar 1
• 1 citations
  Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications
  Madelyn A. Gillentine, Leandra N. Berry, Robin P. Goin-Kochel, May Ali, Jun Ge, Danielle Guffey, Jill A. Rosenfeld, Vickie L. Hannig, Patricia I. Bader, Monica Proud, ...> ;Journal of Autism and Developmental Disorders. 2017 Feb 6
• 114 citations
  16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
  Kyle J. Steinman, Sarah J. Spence, Melissa B. Ramocki, Monica Proud, Sudha Kilaru Kessler, Elysa J. Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K. ...> ;American Journal of Medical Genetics. Part A. 2016 Nov 1
• Developmental trajectories of deep gray matter structures in healthy children and adults.
  Stosic, M.,Han, X.,Haque, M.,Torres, L.,Reynolds, J.,Rogers, A.,Jones, J.,Proud, M.,Hasan, K. M.,Maletić-Savatić, M.> ;Int. J. Dev. Neurosci.. 2015 Nov 05
• 20 citations
  Prevalence of Autism Spectrum Disorder in Children Referred for Diagnostic Autism Evaluation
  Sonia A. Monteiro, Adiaha Spinks-Franklin, Diane Treadwell-Deering, Leandra N. Berry, Sherry Sellers-Vinson, Eboni M. Smith, Monica Proud, Robert G. Voigt> ;Clinical Pediatrics. 2015 Jun 29
• 194 citations
  A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
  Flore Zufferey, Elliott H. Sherr, Noam D. Beckmann, Ellen Hanson, Anne M. Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux, Eli...> ;Journal of Medical Genetics. 2012 Oct 1
• 42 citations
  Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44
  Sandesh C.S. Nagamani, Ayelet Erez, Carolyn Bay, Anjana L. Pettigrew, Seema R. Lalani, Kristin Herman, Brett H. Graham, Małgorzata J.M. Nowaczyk, Monica Proud, William...> ;European Journal of Human Genetics. 2012 Feb 1
• 363 citations
  Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
  Marwan Shinawi, Pengfei Liu, Sung Hae L. Kang, Joseph J. Shen, John W. Belmont, Daryl A. Scott, Frank J. Probst, William J. Craigen, Brett H. Graham, Amber Pursley, Ga...> ;Journal of Medical Genetics. 2010 May 1
• 47 citations
  A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder.
  Jaime M. Williams, Tyler F. Beck, David M. Pearson, Monica Proud, Sau Wai Cheung, Daryl A. Scott> ;American Journal of Medical Genetics. Part A. 2009 Aug 1
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