Brian Paul

Dr. Brian Paul

University of Iowa Carver College of Medicine
orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 January 2022 in Biology
Verified
Journal Article
Open access
PDF file
AAAngelo Antiguas
Angelo Antiguas
BPBrian Paul
Brian Paul
Martine DunnwaldMartine Dunnwald
Martine Dunnwald
Morphogenesis requires a tight coordination between mechanical forces and biochemical signals to inform individual cellular behavior. For these developmental processes to happen correctly the organism requires precise spatial and temporal coordination of the adhesion, migration, growth, differentiation, and apoptosis of cells originating from the three key embryonic layers, namely the ectoderm, mesoderm, and endoderm. The cytoskeleton and its remodeling are essential to organize and amplify many of the signaling pathways required for proper morphogenesis. In particular, the interaction of the cell junctions with the cytoskeleton functions to amplify the behavior of individual cells into collective events that are critical for development. In this review we summarize the key morphogenic events that occur during the formation of the face and the palate, as well as the protein complexes required for cell-to-cell adhesions. We then integrate the current knowledge into a comprehensive review of how mutations in cell-to-cell adhesion genes lead to abnormal craniofacial development, with a particular focus on cleft lip with or without cleft palate.

27 March 2021 in Developmental Dynamics
Verified
Journal Article
Closed access
PDF file
BPBrian Paul
Brian Paul
KPKristina J. Palmer
Kristina J. Palmer
LRLindsey Rhea
Lindsey Rhea
MCMelissa Carlson
Melissa Carlson
JSJocelyn C. Sharp
Jocelyn C. Sharp
Martine DunnwaldMartine Dunnwald
Martine Dunnwald

7 May 2026 in Journal of Plastic, Reconstructive & Aesthetic Surgery
Verified
Journal Article
Closed access
CCColton Connor
Colton Connor
JKJacob Y. Katsnelson
Jacob Y. Katsnelson
BPBrian Paul
Brian Paul
AMAlexander L. Mostovych
Alexander L. Mostovych
QCQuinton Carr
Quinton Carr
RSRyan L. Shapiro
Ryan L. Shapiro

9 February 2026 in Lymphatics
Verified
Journal Article
Open access
PDF file
AJAndrew J. James
Andrew J. James
QCQuinton Carr
Quinton Carr
CCColton Connor
Colton Connor
BPBrian Paul
Brian Paul
CLChristian Laurent
Christian Laurent
RSRyan Shapiro
Ryan Shapiro
Breast cancer-related lymphedema (BCRL) is a chronic and debilitating complication of breast cancer treatment, commonly associated with mastectomy, axillary lymph node dissection, and adjuvant radiation therapy. Though demographic and treatment-related risk factors for BCRL are well documented, emerging evidence suggests that certain genetic polymorphisms may predispose some patients to developing the condition. This review aims to summarize the current research regarding the genetic variants implicated in the development and severity of BCRL. Several candidate genes related to lymphangiogenesis, inflammation, immune cell activation, and lymphatic contractility have been identified. Unfortunately, the existing literature remains limited by the small number of manuscripts, modest sample sizes, and heterogeneous methodologies of available studies. However, further research may shed light on screening options and lead to more personalized treatment strategies to mitigate the incidence and severity of secondary lymphedema.