Publications by authors named "Stuart B Bauer"

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Variability in the Diagnosis and Treatment of Interstitial Cystitis/Bladder Pain Syndrome: Internet Survey.
Eleanora Melkonian, A Leigh Garrett, Erika Kline, Pressley Smith, Madelyn Wiesenhahn, Stuart B Bauer

JMIR Form Res· August 2025

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Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
Lea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, Nils David Mertens, Steve Seltzsam, Stuart B Bauer

Genet Med· July 2025

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Editorial Comment on "Correlation not Causation-Looking Back at the History of VUR".
Stuart B Bauer

Urology· November 2024

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Expert Consensus on Pediatric Urodynamics Reporting Using Modified Delphi Technique.
Kristen M Meier, Claudia Mata, Jill L Kaar, Adam J Rensing, Anne G Dudley, Stuart B Bauer

J Urol· July 2024

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Reply by Authors.
Kristen M Meier, Claudia Mata, Jill L Kaar, Adam J Rensing, Anne G Dudley, Stuart B Bauer

J Urol· July 2024

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The impact of clean intermittent catheterization on students and families in the school environment.
Stuart B Bauer, Kennary Choung, Paige Sable, Blair S Dykeman, Alyssia Venna

Neurourol Urodyn· November 2023

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Facilitators and challenges to transitioning to self-catheterization: Patient and caregiver perspectives.
Lillian C Hayes, Rachel A Saunders, Kennary Choung, Saafia N Masoom, Diane E Price, Stuart B Bauer

Neurourol Urodyn· August 2023

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Accuracy of contrast-enhanced voiding urosonography using Optison™ for diagnosis of vesicoureteral reflux in children.
Harriet J Paltiel, Carol E Barnewolt, Jeanne S Chow, Stuart B Bauer, David A Diamond

J Pediatr Urol· February 2023

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The art of introducing clean intermittent catheterization: How families respond and adapt: A qualitative study.
Stuart B Bauer, Rachel A Saunders, Saafia N Masoom, Kennary Choung, Lillian C Hayes

Neurourol Urodyn· January 2023

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Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Chen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Stuart B Bauer

Eur Urol Open Sci· October 2022

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Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.
Bixia Zheng, Steve Seltzsam, Chunyan Wang, Luca Schierbaum, Sophia Schneider, Stuart B Bauer

Nephrol Dial Transplant· September 2022

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Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Steve Seltzsam, Chunyan Wang, Bixia Zheng, Nina Mann, Dervla M Connaughton, Stuart B Bauer

Genet Med· February 2022

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A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
Bixia Zheng, Chunyan Wang, Steve Seltzsam, Sophia Schneider, Luca Schierbaum, Stuart B Bauer

Am J Med Genet A· January 2022

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Onabotulinumtoxin A (Botox): A reasonable alternative for refractory neurogenic bladder dysfunction in children and young adults.
Kenneth A Softness, Hatim Thaker, Didi Theva, Archana Rajender, Bartley G Cilento, Stuart B Bauer

Neurourol Urodyn· November 2021

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Editorial Comment.
Stuart B Bauer

J Urol· May 2021

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Losartan prevents bladder fibrosis and protects renal function in rat with neurogenic paralysis bladder.
Yu L He, Jian G Wen, Qing S Pu, Yi B Wen, Rong Q Zhai, Stuart B Bauer

Neurourol Urodyn· January 2021

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Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT).
Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, Dervla M Connaughton, Rufeng Dai, Stuart B Bauer

Genet Med· October 2020

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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Dervla M Connaughton, Rufeng Dai, Danielle J Owen, Jonathan Marquez, Nina Mann, Stuart B Bauer

Am J Hum Genet· October 2020

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Anxiety, distress, and pain in pediatric urodynamics.
Julia B Finkelstein, Dylan Cahill, Kelsey Graber, Kelsey Tulley, Brianna O'Connell, Stuart B Bauer

Neurourol Urodyn· April 2020

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CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations.
Nina Mann, Franziska Kause, Erik K Henze, Anant Gharpure, Shirlee Shril, Stuart B Bauer

Am J Hum Genet· December 2019

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Editorial Comment.
Stuart B Bauer

J Urol· January 2019

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Pelvic floor laxity: A not so rare but unrecognized form of daytime urinary incontinence in peripubertal and adolescent girls.
Stuart B Bauer, Evalynn Vasquez, Marc Cendron, May M Wakamatsu, Jeanne S Chow

J Pediatr Urol· December 2018

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ICS educational module: Pressure flow study in children.
Jian G Wen, Jens C Djurhuus, Peter F W M Rosier, Stuart B Bauer

Neurourol Urodyn· November 2018

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ICS educational module: Cystometry in children.
Jian G Wen, Jens Christian Djurhuus, Peter F W M Rosier, Stuart B Bauer

Neurourol Urodyn· November 2018

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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Stuart B Bauer

J Am Soc Nephrol· September 2018

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