Monica B. Proud, MD
- Specialty Care/Health Center
Assistant Professor of Pediatrics, Neurology
Baylor College of Medicine
|Baylor College of Medicine||fellowship||Pediatric Neurology||2009|
|Baylor College of Medicine||residency||Pediatrics||2006|
|Georgetown University School of Medicine||medical school||Doctor of Medicine||2004|
About Monica Proud
Dr. Proud seeks to provide excellent pediatric neurologic care and quality in a patient's experience. She strives to use medical knowledge and experience to achieve the best care possible. She values the doctor-patient relationship and respects each patient and family member. Communication is important to her, and she aims to provide enough time and attention to have patients and family understand their medical condition and treatment options.
Dr. Proud has interest in all areas of Pediatric Neurology, but has particular interest in disorders of development and Autism Spectrum.
She is bilingual, communicating well in both English and Spanish.
|American Academy of Neurology||Member|
|American Academy of Pediatrics||Member|
|Child Neurology Society||Member|
|Texas Medical Association||Member|
Monteiro SA, Spinks-Franklin A, Treadwell-Deering D, Berry L, Sellers-Vinson S, Smith E, Proud M, Voigt RG. Prevalence of Autism Spectrum Disorder in Children Referred for Diagnostic Autism Evaluation. Clinical Pediatrics (Phila). 2015 Dec;54(14):1322-7. doi: 10.1177/0009922815592607. Epub 2015 Jun 29. PMID: 26130396.
Nagamani SC, Erez A, Bay C, Pettigrew A, Lalani SR, Herman K, Graham BH, Nowaczyk MJ, Proud M, Craigen WJ, Hopkins B, Kozel B, Plunkett K, Hixson P, Stankiewicz P, Patel A, Cheung SW. Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44. European Journal of Human Genetics 2012 Feb;20(2):176-9. doi: 10.1038/ejhg.2011.171. Epub 2011 Sep 21. PMID: 21934713.
Shinawi M, Liu P, Kang SH, Shen J, Belmont JW, Scott DA, Probst FJ, Craigen WJ, Graham BH, Pursley A, Clark G, Lee J, Proud M, Stocco A, Rodriguez DL, Kozel BA, Sparagana S, Roeder ER, McGrew SG, Kurczynski TW, Allison LJ, Amato S, Savage S, Patel A, Stankiewicz P, Beaudet AL, Cheung SW, Lupski JR. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. Journal of Medical Genetics 2010 May;47(5):332-41. doi: 10.1136/jmg.2009.073015. Epub 2009 Nov 12. PMID: 19914906.
Williams JM, Beck TF, Pearson DM, Proud MB, Cheung SW, Scott DA. A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder. American Journal of Medical Genetics Part A 2009 Aug;149A(8):1758-62. doi: 10.1002/ajmg.a.32941.
Nagamani SC, Erez A, Bay C, Pettigrew A, Lalani SR, Herman K, Graham BH, Nowaczyk MJ, Proud M, Craigen WJ, Hopkins B, Kozel B, Plunkett K, Hixson P, Stankiewicz P, Patel A, Cheung SW. Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44. European Journal of Human Genetics 2012 Feb;20(2):176-9. doi: 10.1038/ejhg.2011.171. Epub 2011 Sep 21.