🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Przemysław Szafrański

Baylor College of Medicine

ORCID: 0000-0002-3886-2971

Also affiliated with 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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 13 papers. Top paper: “Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins”.

Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins

Journal of Molecular Diagnostics(2020)10.1016/j.jmoldx.2019.12.007
N/A
0DataRank · unranked
26 citations

Qian Liu, Nina Guanyi Xie, Lucia R. Wu, Gustavo Rocha, Susana Fernandes +14 more

Perturbation of semaphorin and VEGF signaling in ACDMPV lungs due to FOXF1 deficiency

Respiratory Research(2021)10.1186/s12931-021-01797-7
N/A
0DataRank · unranked
35 citations

Tomasz Gambin, Przemysław Szafrański, Rebecca L. Maywald, Edwina J. Popek, Jason D. Heaney +2 more

Lung‐specific distant enhancer cis regulates expression ofFOXF1and lncRNAFENDRR

Human Mutation(2021)10.1002/humu.24198
N/A
0DataRank · unranked
32 citations

Tomasz Gambin, Justyna A. Karolak, Edwina J. Popek, Paweł Stankiewicz, Przemysław Szafrański

Potential interactions between the TBX4-FGF10 and SHH-FOXF1 signaling during human lung development revealed using ChIP-seq

Respiratory Research(2021)10.1186/s12931-021-01617-y
N/A
0DataRank · unranked
25 citations

Tomasz Gambin, Przemysław Szafrański, Paweł Stankiewicz, Justyna A. Karolak

Ultra-conserved non-coding sequences within the FOXF1 enhancer are critical for human lung development

Genes & Diseases(2022)10.1016/j.gendis.2022.05.002
N/A
0DataRank · unranked
21 citations

Tadeusz Majewski, Esra Yıldız Bölükbaşı, Tomasz Gambin, Justyna A. Karolak, Nahir Cortes‐Santiago +5 more

High‐level gonosomal mosaicism for a pathogenic non‐coding CNV deletion of the lung‐specific FOXF1 enhancer in an unaffected mother of an infant with ACDMPV

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.2062
N/A
0DataRank · unranked
6 citations

Justyna A. Karolak, Przemysław Szafrański, Tomasz Gambin, Nicholas Willard, Steven H. Abman +4 more

Do paternal deletions involving the FOXF1 locus on chromosome 16q24.1 manifest with more severe non-lung anomalies?

European Journal of Medical Genetics(2022)10.1016/j.ejmg.2022.104519
N/A
0DataRank · unranked
5 citations

Justyna A. Karolak, Tomasz Gambin, Przemysław Szafrański, Gail Deutsch, Paweł Stankiewicz +1 more

Diminished TMEM 100 Expression in a Newborn With Acinar Dysplasia and a Novel TBX4 Variant: A Case Report

Pediatric and Developmental Pathology(2023)10.1177/10935266231213464
N/A
0DataRank · unranked
6 citations

Silvia Patrizi, Tomasz Gambin, Bushra Afzal, Emily Schlotterbeck, Justyna A. Karolak +4 more

Histologic features and decreased lung FOXF1 gene expression in severe bronchopulmonary dysplasia without a genetic diagnosis of alveolar capillary dysplasia

Pediatric Pulmonology(2023)10.1002/ppul.26571
N/A
0DataRank · unranked
2 citations

J. Wells Logan, Paweł Stankiewicz, Przemysław Szafrański, Carola Zalles, José L. Gonzáles +4 more

A Small De Novo CNV Deletion of the Paternal Copy of FOXF1, Leaving lncRNA FENDRR Intact, Provides Insight into Their Bidirectional Promoter Region

Non-Coding RNA(2023)10.3390/ncrna9050061
N/A
0DataRank · unranked
2 citations

Paweł Stankiewicz, Przemysław Szafrański

Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia

Clinical Epigenetics(2023)10.1186/s13148-023-01587-6
N/A
0DataRank · unranked
2 citations

Rijutha P. Garimella, Haresh Mani, Ryan Hartman, Gail Deutsch, Alan Silk +3 more

Histologic Features and Decreased Lung FOXF1 Gene Expression in Severe Bronchopulmonary Dysplasia without a Genetic Diagnosis of Alveolar Capillary Dysplasia

(2023)10.22541/au.167635992.24578122/v1
N/A
0DataRank · unranked
0 citations

Csaba Galambos, J. Wells Logan, Paweł Stankiewicz, Przemysław Szafrański, Carola Zalles +4 more

Highly Variable Expressivity of a CNV Deletion Involving TBX4 in Three Deceased Siblings With Lung Developmental Disorder and Their Mildly Affected Mother and Grandfather

Clinical Genetics(2025)10.1111/cge.70010
N/A
0DataRank · unranked
1 citations

Tomasz Gambin, Michał Kadlof, Michał Denkiewicz, Dariusz Plewczyński, Hyun Jeong Kim +5 more