Brendan Lee

Brendan Lee

Baylor College of Medicine

H-index: 93

North America-United States

About Brendan Lee

Brendan Lee, With an exceptional h-index of 93 and a recent h-index of 57 (since 2020), a distinguished researcher at Baylor College of Medicine, specializes in the field of skeletal dysplasia, urea cycle disorder, gene therapy, bone, cartilage.

His recent articles reflect a diverse array of research interests and contributions to the field:

De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities

Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

Nitric oxide is required for lung alveolarization revealed by deficiency of argininosuccinate lyase

Genetic Evaluation for Monogenic Disorders of Low Bone Mass and Increased Bone Fragility: What Clinicians Need to Know

Cranio‐cervical abnormalities in moderate‐to‐severe osteogenesis imperfecta–Genotypic and phenotypic determinants

2023 ASHG presidential address—Reflecting on our 75 years: Acknowledging our past, embracing our present, and dreaming about our future

Psychosocial Outcomes of Pain and Pain Management in Adults with Osteogenesis Imperfecta: A Qualitative Study

A qualitative exploration of patient perspectives on psychosocial burdens and positive factors in adults with osteogenesis imperfecta

Brendan Lee Information

University

Position

___

Citations(all)

30853

Citations(since 2020)

12267

Cited By

23280

hIndex(all)

93

hIndex(since 2020)

57

i10Index(all)

361

i10Index(since 2020)

268

Email

University Profile Page

Baylor College of Medicine

Google Scholar

View Google Scholar Profile

Brendan Lee Skills & Research Interests

skeletal dysplasia

urea cycle disorder

gene therapy

bone

cartilage

Top articles of Brendan Lee

Title

Journal

Author(s)

Publication Date

De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities

American Journal of Medical Genetics Part A

Scott K Ward

Alexandrea Wadley

Chun‐hui Tsai

Paul J Benke

Lisa Emrick

...

2024/1

Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

Genetics in Medicine

Jenna Pucel

Lauren C Briere

Chloe Reuter

Perman Gochyyev

Maria T Acosta

...

2024/6/1

Nitric oxide is required for lung alveolarization revealed by deficiency of argininosuccinate lyase

Human Molecular Genetics

Zixue Jin

Ming-Ming Jiang

Brendan Lee

2024/1/1

Genetic Evaluation for Monogenic Disorders of Low Bone Mass and Increased Bone Fragility: What Clinicians Need to Know

Emily Busse

Brendan Lee

Sandesh Nagamani

2024/4/11

Cranio‐cervical abnormalities in moderate‐to‐severe osteogenesis imperfecta–Genotypic and phenotypic determinants

Orthodontics & Craniofacial Research

Juliana Marulanda

Jean‐Marc Retrouvey

Brendan Lee

V Reid Sutton

BBDC

...

2024/4

2023 ASHG presidential address—Reflecting on our 75 years: Acknowledging our past, embracing our present, and dreaming about our future

The American Journal of Human Genetics

Brendan Lee

2024/3/7

Psychosocial Outcomes of Pain and Pain Management in Adults with Osteogenesis Imperfecta: A Qualitative Study

Journal of Clinical Psychology in Medical Settings

Whitney S Shepherd

Andrew D Wiese

Hannah E Cho

W Conor Rork

M Usman Baig

...

2024/1/28

A qualitative exploration of patient perspectives on psychosocial burdens and positive factors in adults with osteogenesis imperfecta

American Journal of Medical Genetics Part A

W Conor Rork

Alyssa G Hertz

Andrew D Wiese

Kristin M Kostick

Dianne Nguyen

...

2023/9

Celebrating excellence, acknowledging past harms: Both are vital parts of ASHG’s continuing journey to advance human genetics

The American Journal of Human Genetics

Bruce R Korf

Brendan Lee

Mona V Miller

2023/3/2

RNA sequencing as a diagnostic tool

JAMA

Shamika Ketkar

Lindsay C Burrage

Brendan Lee

2023/1/3

Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling

Plos Genetics

Ronit Marom

Bo Zhang

Megan E Washington

I-Wen Song

Lindsay C Burrage

...

2023/11/7

Boosting glycolysis to combat fragile bone in type 1 diabetes

Cell Chemical Biology

Zixue Jin

Brendan Lee

2023/9/21

Argininosuccinate lyase deficiency causes blood-brain barrier disruption via nitric oxide–mediated dysregulation of claudin expression

JCI insight

Jordan Kho

Urszula Polak

Ming-Ming Jiang

John D Odom

Jill V Hunter

...

2023/9/9

What has the undiagnosed diseases network taught us about the clinical applications of genomic testing?

David R Murdock

Jill A Rosenfeld

Brendan Lee

2022/1/27

Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers–Danlos syndrome

Human Molecular Genetics

Keren Machol

Urszula Polak

Monika Weisz-Hubshman

I-Wen Song

Shan Chen

...

2022/4/15

Yap and Taz promote osteogenesis and prevent chondrogenesis in neural crest cells in vitro and in vivo

Science signaling

Xiaolei Zhao

Li Tang

Tram P Le

Bao H Nguyen

Wen Chen

...

2022/10/25

Helper-dependent adenoviral gene therapy delivery and expression system

2023/9/5

Targeting TGF-β for treatment of osteogenesis imperfecta

The Journal of clinical investigation

I-Wen Song

Sandesh CS Nagamani

Dianne Nguyen

Ingo Grafe

Vernon Reid Sutton

...

2022/4/1

DDRGK1 is required for the proper development and maintenance of the growth plate cartilage

Human Molecular Genetics

Monika Weisz-Hubshman

Adetutu T Egunsula

Brian Dawson

Alexis Castellon

Ming-Ming Jiang

...

2022/8/15

Double-spin leukocyte-rich platelet-rich plasma is predominantly lymphocyte rich with notable concentrations of other white blood cell subtypes

Arthroscopy, Sports Medicine, and Rehabilitation

Anuj Marathe

Shiv J Patel

Bo Song

Joseph M Sliepka

Theodore S Shybut

...

2022/4/1

See List of Professors in Brendan Lee University(Baylor College of Medicine)