Brendan Lee

Also affiliated with Texas Children's Hospital, Baylor Genetics

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 5%percentile

0.545Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Research for all: building a diverse researcher community for the All of Us Research Program

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae270

Top 36%

0.545DataRank

Top 36%10 citations

Minnkyong Lee, Sydney McMaster, Jessica M. Lee, Faith Blackburne-Proctor, Romuladus E. Azuine +41 more

Papers

Driven by 77 papers — median percentile 64. Top paper: “Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations”.

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Genetics in Medicine(2021)10.1038/s41436-021-01232-8

N/A

1.3DataRank · unranked

49 citations

Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra +92 more

4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta

Journal of Bone and Mineral Research(2020)10.1002/jbmr.4501

N/A

1.1DataRank · unranked

38 citations

Jennifer Zieba, Fabiana Csukasi, Jorge Martı́n, Davis Wachtell, Maya Barad +9 more

SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia

Brain(2023)10.1093/brain/awac460

N/A

0.992DataRank · unranked

35 citations

Hagar Mor Shaked, Kenneth Gable, Sita D. Gupta, Xueyang Pan, Niranjanakumari Somashekarappa +93 more

Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing

Journal of Clinical Investigation(2020)10.1172/jci141500

N/A

0.788DataRank · unranked

190 citations

Hongzheng Dai, Lindsay C. Burrage, Jill A. Rosenfeld, Shamika Ketkar, Michaela Müller +13 more

Health‐related quality of life in adults with osteogenesis imperfecta

Clinical Genetics(2021)10.1111/cge.13939

N/A

0.786DataRank · unranked

28 citations

Brady Slater, Salma Musaad, David Cuthbertson, Dianne Nguyen, Alicia Turner +7 more

Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency

JCI Insight(2020)10.1172/jci.insight.132342

N/A

0.769DataRank · unranked

14 citations

Simran Madan, Xiaohui Li, Saima Ali, Mahmoud A. Mohammad, Bridget M. Stroup +17 more

Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

Neuron(2020)10.1016/j.neuron.2020.02.021

N/A

0.767DataRank · unranked

165 citations

Michael F. Wangler, Paul C. Marcogliese, Ju-Yeon Jo, Thomas A. Ravenscroft, Zhongyuan Zuo +29 more

Malocclusion traits and oral health–related quality of life in children with osteogenesis imperfecta

The Journal of the American Dental Association(2020)10.1016/j.adaj.2020.03.040

N/A

0.762DataRank · unranked

24 citations

Sreenath Madathil, Frank Rauch, V. Reid Sutton, Brendan Lee, Jean-Marc Retrouvey +19 more

Targeting TGF-β for treatment of osteogenesis imperfecta

Journal of Clinical Investigation(2022)10.1172/jci152571

N/A

0.678DataRank · unranked

91 citations

Sandesh C.S. Nagamani, Dianne Nguyen, Ingo Grafe, V. Reid Sutton, Francis H. Gannon +16 more

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Genetics in Medicine(2020)10.1038/s41436-020-01027-3

N/A

0.587DataRank · unranked

49 citations

Kirsty McWalter, Heleen te Brinke, Lodewijk IJlst, Petra M. Mooijer, Jos P.N. Ruiter +95 more

Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Genetics in Medicine(2020)10.1038/s41436-020-00984-z

N/A

0.564DataRank · unranked

42 citations

Cecilia Esteves, Anna Bican, Rebecca C. Spillmann, Heidi Cope, Allyn McConkie‐Rosell +89 more

COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.002

N/A

0.561DataRank · unranked

41 citations

Lindsay C. Burrage, Rossella Venditti, Aurélie Clément, Bernardo Blanco‐Sánchez, Mahim Jain +48 more

Research for all: building a diverse researcher community for the All of Us Research Program

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae270

Top 36%

0.545DataRank

Top 36%10 citations

Minnkyong Lee, Sydney McMaster, Jessica M. Lee, Faith Blackburne-Proctor, Romuladus E. Azuine +41 more

The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.007

N/A

0.510DataRank · unranked

29 citations

Sen Zhao, Jefferson C. Sinson, Aleksandar Bajić, Jill A. Rosenfeld, Matthew B. Neeley +23 more

A novel de novo intronic variant in ITPR1 causes Gillespie syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62232

N/A

0.434DataRank · unranked

17 citations

Ming‐Ming Jiang, Xiaohui Li, Ronit Marom, Hongzheng Dai, David R. Murdock +16 more

Machine learning in time-lapse imaging to differentiate embryos from young vs old mice

Biology of Reproduction(2024)10.1093/biolre/ioae056

N/A

0.330DataRank · unranked

8 citations

Carolina Leynes, Ashley Pawelka, Isabel Lorenzo, Andrew Chou, Brendan Lee +2 more

Generation of a humanized mAce2 and a conditional hACE2 mouse models permissive to SARS-COV-2 infection

Mammalian Genome(2024)10.1007/s00335-024-10033-8

N/A

0.292DataRank · unranked

6 citations

Megan Washington, Carolina Leynes, Jason Hsu, Kempaiah Rayavara, Yangjin Bae +12 more

A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay

Human Mutation(2022)10.1002/humu.24497

N/A

0.292DataRank · unranked

6 citations

Wenmiao Zhu, Bo Yuan, Nicole Walley, Kelly Schoch, Yong‐hui Jiang +10 more

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121

N/A

0.292DataRank · unranked

6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

Resilience and coping: a qualitative analysis of cognitive and behavioral factors in adults with osteogenesis Imperfecta

Disability and Rehabilitation(2024)10.1080/09638288.2024.2358903

N/A

0.269DataRank · unranked

5 citations

Whitney S. Shepherd, Gianna M. Colombo, Andrew D. Wiese, W. Conor Rork, Kristin M. Kostick +10 more

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

Current Osteoporosis Reports(2024)10.1007/s11914-024-00870-6

N/A

0.247DataRank · unranked

4 citations

Brendan Lee, Sandesh C.S. Nagamani, Emily Busse

PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62704

N/A

0.241DataRank · unranked

4 citations

David R. Murdock, Lindsay C. Burrage, Hongzheng Dai, Seema R. Lalani, Richard A. Lewis +10 more

The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.013

N/A

0.208DataRank · unranked

3 citations

Jefferson C. Sinson, Shenglan Li, Jill A. Rosenfeld, Gladys Zapata, Kristina Macakova +15 more

Experiences in providing a community educational resource for the All of Us Researcher Workbench

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae226

N/A

0.165DataRank · unranked

2 citations

Jinyoung Byun, Jun Wang, Stephen Richards, Pamela N. Luna, LaTerrica Williams +11 more

Designing and implementing solution-oriented team science initiatives—a chronic pain example

Frontiers in Pain Research(2025)10.3389/fpain.2025.1669072

N/A

0.165DataRank · unranked

2 citations

Armen N. Akopian, Kyle D. Allen, Yenisel Cruz-Almeida, Christopher R. Donnelly, Brendan Lee +7 more

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.006

N/A

0DataRank · unranked

37 citations

Tanya L. Schwab, Sarah K. Macklin‐Mantia, A. Reghan Foley, Filippo Pinto e Vairo, Davut Pehli̇van +25 more

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

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63323

N/A

0DataRank · unranked

13 citations

Alyssa Hertz, Andrew D. Wiese, Kristin M. Kostick, Dianne Nguyen, Sophie C. Schneider +8 more

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

JCI Insight(2023)10.1172/jci.insight.168475

N/A

0DataRank · unranked

12 citations

Urszula Polak, Ming‐Ming Jiang, John D. Odom, Jill V. Hunter, Saima Ali +8 more

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

PLoS Genetics(2023)10.1371/journal.pgen.1011005

N/A

0DataRank · unranked

12 citations

Bo Zhang, Megan Washington, I-Wen Song, Lindsay C. Burrage, Vittoria Rossi +28 more

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(2023)10.1002/ajmg.a.63399

N/A

0DataRank · unranked

4 citations

Alexandrea Wadley, Chun-Hui Tsai, Paul J. Benke, Lisa Emrick, Kristen Fisher +15 more

Delayed skeletal development and IGF-1 deficiency in a mouse model of lysinuric protein intolerance

Disease Models & Mechanisms(2023)10.1242/dmm.050118

N/A

0DataRank · unranked

3 citations

Xiaohui Li, Sara Ho, Haonan Zhouyao, Yuqing Chen, Safa Ani +14 more

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

Human Molecular Genetics(2023)10.1093/hmg/ddad158

N/A

0DataRank · unranked

1 citations

Ming‐Ming Jiang, Brendan Lee, Zixue Jin

Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy

medRxiv(2023)10.1101/2023.03.27.23287689

N/A

0DataRank · unranked

3 citations

Sydney L. Michener, Hongling Pan, Jessica M. Pfliger, Jill A. Rosenfeld, Vanesa Lerma +40 more

Reducing Time to Diagnosis of Rare Genetic Diseases in a Medically Underserved Hispanic Population- Lessons Learned for Meaningful Engagement

Research Square(2023)10.21203/rs.3.rs-3699740/v1

N/A

0DataRank · unranked

3 citations

Roberta Sierra, Dan Brooks, Christopher J. Holder, Lauren Urbanski, Keila Rodriguez +19 more

AI-MARRVEL — A Knowledge-Driven AI System for Diagnosing Mendelian Disorders

NEJM AI(2024)10.1056/aioa2300009

N/A

0DataRank · unranked

45 citations

Chaozhong Liu, Linhua Wang, Rami AI-Ouran, Cole A. Deisseroth, Sasidhar Pasupuleti +18 more

The IFITM5 mutation in osteogenesis imperfecta type V is associated with an ERK/SOX9-dependent osteoprogenitor differentiation defect

Journal of Clinical Investigation(2024)10.1172/jci170369

N/A

0DataRank · unranked

10 citations

I-Wen Song, Emily Busse, Megan Washington, Ava S. Berrier, Vittoria Rossi +27 more

Project GIVE: using a virtual genetics service platform to reduce health inequities and improve access to genomic care in an underserved region of Texas

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09560-x

N/A

0DataRank · unranked

5 citations

Roberta Sierra, Daniel Brooks, Christopher J. Holder, Lauren Urbanski, Keila Rodriguez +20 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

Qualitative investigation of school experiences in children with osteogenesis imperfecta

Children s Health Care(2024)10.1080/02739615.2024.2403482

N/A

0DataRank · unranked

3 citations

Andrew D. Wiese, Whitney S. Shepherd, Gianna M. Colombo, Selena Guo, Justin Qian +14 more

Development and evaluation of a training curriculum to engage researchers on accessing and analyzing the All of Us data

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae240

N/A

0DataRank · unranked

3 citations

Jasmine N Baker, Shamika Ketkar, Ashley M. Butler, LaTerrica Williams, Latanya Hammonds-Odie +5 more

Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing

Human Molecular Genetics(2024)10.1093/hmg/ddae105

N/A

0DataRank · unranked

1 citations

Shamika Ketkar, Taotao Tan, Elizabeth G. Atkinson, Lindsay C. Burrage, Kim C. Worley +6 more

Clinical validation of RNA sequencing for Mendelian disorder diagnostics

medRxiv(2024)10.1101/2024.08.15.24312057

N/A

0DataRank · unranked

2 citations

Kristina Macakova, Jefferson Sinson, Hongzheng Dai, Jill A. Rosenfeld, Gladys Zapata +10 more

Mindful self-compassion to reduce pain interference among adults with osteogenesis imperfecta

Research Square(2024)10.21203/rs.3.rs-4582869/v1

N/A

0DataRank · unranked

0 citations

Roya Al-Khalili, Saunya Dover, Corien Peeters, Adam Khalif, V. Reid Sutton +5 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more

A standardized, open-source, portable model for noninvasive joint injury in mice

Osteoarthritis and Cartilage Open(2025)10.1016/j.ocarto.2025.100679

N/A

0DataRank · unranked

2 citations

Lindsey Lammlin, Sofia Gonzalez-Nolde, Scarlet Howser, I Smith, Luke Stasikelis +94 more

The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder Diagnostics

medRxiv(2025)10.1101/2025.01.28.25321295

N/A

0DataRank · unranked

1 citations

Jefferson Sinson, Shenglan Li, Jill A. Rosenfeld, Gladys Zapata, Kristina Macakova +16 more

C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder

Genetics in Medicine(2025)10.1016/j.gim.2025.101429

N/A

0DataRank · unranked

0 citations

Laura Mackay, Maria Blazo, Elizabeth Mizerik, Jozef Gécz, Renée Carroll +34 more

Mechanical characterization of Col1a1 osteogenesis imperfecta bone revealed altered mechanical stiffness heterogeneity across scales

Cell Biomaterials(2025)10.1016/j.celbio.2025.100246

N/A

0DataRank · unranked

0 citations

Ellen Busschers, Hutomo Tanoto, Anoushka Prabhu, Thế Dũng Bùi, Phuc Van Nguyen +9 more

Osteogenesis imperfecta and the family: A qualitative analysis of the experiences of family and caregivers.

Families Systems & Health(2025)10.1037/fsh0001004

N/A

0DataRank · unranked

0 citations

Andrew D. Wiese, Amelia Mercado, Whitney S. Shepherd, Michelle L. Fynan, Kara Ayers +14 more

Implementing a training resource for large-scale genomic data analysis in the All of Us Researcher Workbench

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.018

N/A

0DataRank · unranked

0 citations

Erik Stricker, Julie Coleman, Shamika Ketkar, Taotao Tan, Ashley M. Butler +7 more

KneEZ Clear, an Effective Tissue Clearing Protocol to Study Musculoskeletal Tissues in the Mouse

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.08.13.670136

N/A

0DataRank · unranked

0 citations

Taeyong Ahn, Luis Tovias, Azeez Ishola, Carolina Leynes, Jason M Kirk +7 more

Two commonly reported incidental variants in OTC are associated with late-onset disease

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100531

N/A

0DataRank · unranked

0 citations

Russell S. Lo, Gareth A. Cromie, Aimée M. Dudley, Nicholas Ah Mew, Kara Simpson +9 more

Integrative exome sequencing and machine learning identify MICB and interferon pathway genes as contributors to SSc risk

Annals of the Rheumatic Diseases(2025)10.1016/j.ard.2025.05.009

N/A

0DataRank · unranked

1 citations

Hongzheng Dai, Lindsay C. Burrage, David R. Murdock, Brian Dawson, Marialbert Acosta‐Herrera +9 more

Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiation

Journal of Clinical Investigation(2020)10.1172/jci138935

N/A

0DataRank · unranked

82 citations

Jordan Kho, Brian Dawson, Ming‐Ming Jiang, Yuqing Chen, Saima Ali +8 more

A global Slc7a7 knockout mouse model demonstrates characteristic phenotypes of human lysinuric protein intolerance

Human Molecular Genetics(2020)10.1093/hmg/ddaa107

N/A

0DataRank · unranked

18 citations

Ronit Marom, Xiaohui Li, Chih‐Wei Hsu, Cheng‐Yen Chang, Luan D. Truong +17 more

Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profiles

Bone(2020)10.1016/j.bone.2020.115547

N/A

0DataRank · unranked

12 citations

Marie‐Eve Robinson, Cristián Seiltgens, V. Reid Sutton, Brendan Lee, Francis H. Glorieux +2 more

Fracture Healing in Collagen-Related Preclinical Models of Osteogenesis Imperfecta

Journal of Bone and Mineral Research(2020)10.1002/jbmr.3979

N/A

0DataRank · unranked

26 citations

Elda Munivez, Alexis Castellon, Ming-Ming Jiang, Brian Dawson, Catherine G. Ambrose +2 more

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

Science Translational Medicine(2020)10.1126/scitranslmed.aav9166

N/A

0DataRank · unranked

25 citations

Damon T. Burrow, Jinmei Li, Jiwoong Park, Sandeep Kumar, Cheng Lyu +33 more

Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice

Human Molecular Genetics(2020)10.1093/hmg/ddz307

N/A

0DataRank · unranked

1 citations

Danielle Veenma, Oleg A. Shchelochkov, Zhiyin Yu, Bum‐Joon Kim, Hitisha P. Zaveri +12 more

COPB2 haploinsufficiency causes a coatopathy with osteoporosis and developmental delay

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.14.297234

N/A

0DataRank · unranked

1 citations

Lindsay C. Burrage, Aurélie Clément, Bernardo Blanco‐Sánchez, Rossella Venditti, Mahim Jain +49 more

Heterozygous variants in SPTBN1 cause intellectual disability and autism

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62201

N/A

0DataRank · unranked

28 citations

Rui Xiao, Mir Reza Bekheirnia, Farah Kanani, Michael Parker, Mary Kay Koenig +17 more

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(2021)10.1016/j.asmr.2021.10.004

N/A

0DataRank · unranked

24 citations

Shiv Patel, Bo Song, Joseph M. Sliepka, Theodore B. Shybut, Brendan Lee +2 more

Osteogenesis imperfecta tooth level phenotype analysis: Cross-sectional study

Bone(2021)10.1016/j.bone.2021.115917

N/A

0DataRank · unranked

19 citations

Hanan Moussa, Timothy Schwinghamer, Maxime Ducret, Didem Dagdeviren, Jean-Marc Retrouvey +23 more

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

Human Molecular Genetics(2021)10.1093/hmg/ddab323

N/A

0DataRank · unranked

11 citations

Urszula Polak, Monika Weisz‐Hubshman, I-Wen Song, Shan Chen, Ming‐Ming Jiang +6 more

Novel Assessment of Leukocyte-Rich Platelet-Rich Plasma on Functional and Patient-Reported Outcomes in Knee Osteoarthritis: A Pilot Study

Regenerative Medicine(2021)10.2217/rme-2021-0032

N/A

0DataRank · unranked

11 citations

Gu Eon Kang, Brett Heldt, Olumide F. Sokunbi, Bo Song, Peter Yeh +5 more

A Novel Mouse Model for SNP in Steroid Receptor Co-Activator-1 Reveals Role in Bone Density and Breast Cancer Metastasis

Endocrinology(2021)10.1210/endocr/bqab094

N/A

0DataRank · unranked

9 citations

Konstantinos Verdelis, Peter C. Lucas, Shiming Jiang, Yuqing Chen, Feiqi Lu +16 more

The transcriptional cofactor Jab1/Cops5 is crucial for BMP‐mediated mouse chondrocyte differentiation by repressing p53 activity

Journal of Cellular Physiology(2021)10.1002/jcp.30254

N/A

0DataRank · unranked

6 citations

William E. Samsa, Lindsay A. Bashur, Yuqing Chen, Ricky Chan, Brendan Lee +2 more

Yap and Taz function as the osteochondrogenic determinant in neural crest cells

The FASEB Journal(2021)10.1096/fasebj.2021.35.s1.04713

N/A

0DataRank · unranked

0 citations

Li Tang, Bao Nguyen, Tram P. Le, Wen Chen, Mingjie Zheng +9 more

RNA Sequencing as a Diagnostic Tool

JAMA(2022)10.1001/jama.2022.22843

N/A

0DataRank · unranked

35 citations

Lindsay C. Burrage, Brendan Lee, Shamika Ketkar

What Has the Undiagnosed Diseases Network Taught Us About the Clinical Applications of Genomic Testing?

Annual Review of Medicine(2022)10.1146/annurev-med-042120-014904

N/A

0DataRank · unranked

25 citations

Jill A. Rosenfeld, Brendan Lee, David R. Murdock

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

Human Molecular Genetics(2022)10.1093/hmg/ddac078

N/A

0DataRank · unranked

15 citations

Adetutu T Egunsula, Brian Dawson, Alexis Castellon, Ming‐Ming Jiang, Yuqing Chen-Evenson +4 more

Loading‐induced bone formation is mediated by Wnt1 induction in osteoblast‐lineage cells

The FASEB Journal(2022)10.1096/fj.202200591r

N/A

0DataRank · unranked

14 citations

Nicole Migotsky, Christopher J. Chermside‐Scabbo, John T. Shuster, Kyu Sang Joeng, Roberto Civitelli +3 more

A novel, de novo intronic variant in POGZ causes White–Sutton syndrome

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62747

N/A

0DataRank · unranked

9 citations

David R. Murdock, Jill A. Rosenfeld, Hongzheng Dai, Shamika Ketkar, Lisa Emrick +10 more

Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAP

Bone(2022)10.1016/j.bone.2022.116516

N/A

0DataRank · unranked

5 citations

Karissa Ludwig, Francis H. Glorieux, Brendan Lee, V. Reid Sutton, Jean-Marc Retrouvey +2 more

Wide range of phenotypic severity in individuals with late truncations unique to the predominant CDKL5 transcript in the brain

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62940

N/A

0DataRank · unranked

5 citations

Isabel Haviland, Yoel Gofin, Lindsay C. Swanson, Christelle Moufawad El Achkar, John M. Schreiber +21 more

Yap and Taz promote osteogenesis in neural crest cells by preventing chondrogenesis

The FASEB Journal(2022)10.1096/fasebj.2022.36.s1.r4623

N/A

0DataRank · unranked

1 citations

Li Tang, Bao Nguyen, Tram P. Le, Wen Chen, Mingjie Zheng +9 more

Loading-Induced Bone Formation is Mediated by Wnt1 Induction in Osteoblast-Lineage Cells

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.28.482178

N/A

0DataRank · unranked

1 citations

Nicole Migotsky, Christopher J. Chermside‐Scabbo, John T. Shuster, Kyu Sang Joeng, Roberto Civitelli +3 more

Brendan Lee

Indexed papers

Top data-sharing exemplar

Papers