Justyna A. Karolak

1.6k citations

48 papers · 771 indexed · h-index 17

Co-authors: Marzena Gajęcka Małgorzata Rydzanicz Jacek P. Szaflik Dorota Nowak Paweł Stankiewicz Piotr Polakowski Tomasz Gambin Jose A. Pitarque
Topics: Corneal surgery and disorders (17 papers)Corneal Surgery and Treatments (14 papers)Renal and related cancers (10 papers)
Cited by: Ophthalmology Radiology, Nuclear Medicine and Imaging Public Health, Environmental and Occupational Health
Journals: American Journal of Respiratory and Critical Care Medicine Scientific Reports Genome biology
Partner nations: Poland United States Ecuador

In The Last Decade

Justyna A. Karolak

47 papers receiving 757 citations

Peers

Countries citing papers authored by Justyna A. Karolak

Since Specialization

Citations

This map shows the geographic impact of Justyna A. Karolak's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Justyna A. Karolak with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Justyna A. Karolak more than expected).

Fields of papers citing papers by Justyna A. Karolak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Justyna A. Karolak. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Justyna A. Karolak. The network helps show where Justyna A. Karolak may publish in the future.

Co-authorship network of co-authors of Justyna A. Karolak

This figure shows the co-authorship network connecting the top 25 collaborators of Justyna A. Karolak. A scholar is included among the top collaborators of Justyna A. Karolak based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Justyna A. Karolak. Justyna A. Karolak is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	PhaseDancer: a novel targeted assembler of segmental duplications unravels the complexity of the human chromosome 2 fusion going from 48 to 46 chromosomes in hominin evolution 2023 ·Genome biology ·(unknown),Krzysztof Gogolewski,Justyna A. Karolak,Paweł Stankiewicz,Anna Gambin	2
2	Single Cell Multiomics Identifies Cells and Genetic Networks Underlying Alveolar Capillary Dysplasia 2023 ·American Journal of Respiratory and Critical Care Medicine ·Minzhe Guo,Kathryn A. Wikenheiser‐Brokamp,Joseph A. Kitzmiller,(unknown),Guolun Wang,Allen Wang,Sebastian Preißl,Xiaomeng Hou,Justin Buchanan,Justyna A. Karolak,Yifei Miao,David B. Frank,William J. Zacharias,Xin Sun,Yan Xu,Mingxia Gu,Paweł Stankiewicz,Vladimir V. Kalinichenko,(unknown),Jeffrey A. Whitsett	14
3	A novel non‐recurrent CNV deletion involving TBX4 and leaving TBX2 intact causes congenital alveolar dysplasia 2023 ·Clinical Genetics ·(unknown),(unknown),Gail Deutsch,Joseph A. Kitzmiller,Małgorzata Rydzanicz,Rafał Płoski,Jeffrey A. Whitsett,Robert Śmigiel,Justyna A. Karolak	1
4	Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis 2023 ·Genes ·(unknown),Anna Kutkowska‐Kaźmierczak,Gail Deutsch,(unknown),Marta Smyk,(unknown),(unknown),Ewa Obersztyn,Jan Modzelewski,(unknown),Paweł Stankiewicz,Marzena Gajęcka,Małgorzata Rydzanicz,Rafał Płoski,Tomasz Szczapa,Justyna A. Karolak	0
5	Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant 2022 ·European Journal of Human Genetics ·(unknown),Justyna A. Karolak,Przemysław Szafrański,Tomasz Gambin,Admire Matsika,(unknown),Hamish S. Scott,Peer Arts,Thuong Ha,Christopher Barnett,(unknown),Paweł Stankiewicz	2
6	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 2022 ·Molecular Genetics & Genomic Medicine ·(unknown),Justyna A. Karolak,Przemysław Szafrański,Tomasz Gambin,(unknown),Steven H. Abman,Csaba Galambos,John P. Kinsella,Paweł Stankiewicz	4
7	Do paternal deletions involving the FOXF1 locus on chromosome 16q24.1 manifest with more severe non-lung anomalies? 2022 ·European Journal of Medical Genetics ·(unknown),Justyna A. Karolak,Tomasz Gambin,Przemysław Szafrański,Gail Deutsch,Paweł Stankiewicz	3
8	Ultra-conserved non-coding sequences within the FOXF1 enhancer are critical for human lung development 2022 ·Genes & Diseases ·Przemysław Szafrański,Tadeusz Majewski,(unknown),Tomasz Gambin,Justyna A. Karolak,Nahir Cortes‐Santiago,Markus Brückner,Gabriele Amann,(unknown),Paweł Stankiewicz	5
9	Variants in FLRT3 and SLC35E2B identified using exome sequencing in seven high myopia families from Central Europe 2021 ·Advances in Medical Sciences ·(unknown),Justyna A. Karolak,Tomasz Gambin,Małgorzata Rydzanicz,(unknown),Małgorzata Mrugacz,(unknown),Paweł Stankiewicz,James R. Lupski,Marzena Gajęcka	6
10	Genotype–phenotype correlation in two Polish neonates with alveolar capillary dysplasia 2020 ·BMC Pediatrics ·(unknown),(unknown),Joanna Wróblewska,(unknown),Andrzej Marszałek,Yogen Singh,(unknown),Qian Liu,Justyna A. Karolak,Paweł Stankiewicz,Gail Deutsch,(unknown),Tomasz Szczapa	6
11	Further evaluation of differential expression of keratoconus candidate genes in human corneas 2020 ·PeerJ ·Justyna A. Karolak,(unknown),Katarzyna Tomela,Michał Kabza,Dorota Nowak,Małgorzata Rydzanicz,Piotr Polakowski,Jacek P. Szaflik,Marzena Gajęcka	16
12	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 2020 ·Journal of Molecular Diagnostics ·Justyna A. Karolak,Qian Liu,(unknown),Lucia R. Wu,Gustavo Rocha,Susana Fernandes,(unknown),Ivan F. M. Lo,David Mowat,Elizabeth K. Fiorino,Morris Edelman,Joyce E. Fox,Denise A. Hayes,David P. Witte,(unknown),Edwina J. Popek,Przemysław Szafrański,David Y. Zhang,Paweł Stankiewicz	12
13	A de novo 2.2 Mb recurrent 17q23.1q23.2 deletion unmasks novel putative regulatory non-coding SNVs associated with lethal lung hypoplasia and pulmonary hypertension: a case report 2020 ·BMC Medical Genomics ·Justyna A. Karolak,Tomasz Gambin,Engela Honey,Tomáš Slavík,Edwina J. Popek,Paweł Stankiewicz	11
14	Heterozygous CTNNB1 and TBX4 variants in a patient with abnormal lung growth, pulmonary hypertension, microcephaly, and spasticity 2019 ·Clinical Genetics ·Justyna A. Karolak,Przemysław Szafrański,(unknown),Chirag Patel,(unknown),Esther Kinning,Kate Chandler,Shalini N. Jhangiani,Zeynep H. Coban Akdemir,James R. Lupski,Edwina J. Popek,Paweł Stankiewicz	12
15	Clinical, Histopathological, and Molecular Diagnostics in Lethal Lung Developmental Disorders 2019 ·American Journal of Respiratory and Critical Care Medicine ·Marie Vincent,Justyna A. Karolak,Gail Deutsch,Tomasz Gambin,Edwina J. Popek,Bertrand Isidor,Przemysław Szafrański,Cédric Le Caignec,Paweł Stankiewicz	44
16	Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype 2019 ·Human Genetics ·Przemysław Szafrański,Qian Liu,Justyna A. Karolak,Xiaofei Song,Nicole de Leeuw,Brigitte H. W. Faas,(unknown),Petr Janků,Marta Ježová,(unknown),Kathleen Gibbs,Lea F. Surrey,(unknown),Denis Bérubé,Luc L. Oligny,Jacques L. Michaud,Edwina J. Popek,Paweł Stankiewicz	16
17	Novel parent-of-origin-specific differentially methylated loci on chromosome 16 2019 ·Clinical Epigenetics ·(unknown),Przemysław Szafrański,Harry Lesmana,Robert J. Hopkin,Aaron Hamvas,Jennifer Wambach,Marwan Shinawi,Gladys Zapata,Claudia M.B. Carvalho,Qian Liu,Justyna A. Karolak,James R. Lupski,Neil A. Hanchard,Paweł Stankiewicz	14
18	Collagen synthesis disruption and downregulation of core elements of TGF-β, Hippo, and Wnt pathways in keratoconus corneas 2017 ·European Journal of Human Genetics ·Michał Kabza,Justyna A. Karolak,Małgorzata Rydzanicz,Michał Wojciech Szcześniak,Dorota Nowak,(unknown),Piotr Polakowski,Rafał Płoski,Jacek P. Szaflik,Marzena Gajęcka	82
19	Molecular Screening of Keratoconus Susceptibility Sequence Variants inVSX1, TGFBI, DOCK9, STK24, andIPO5Genes in Polish Patients and NovelTGFBIVariant Identification 2014 ·Ophthalmic Genetics ·Justyna A. Karolak,Piotr Polakowski,Jerzy Szaflik,Jacek P. Szaflik,Marzena Gajęcka	33
20	Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus 2011 ·European Journal of Human Genetics ·(unknown),Justyna A. Karolak,Dorota Nowak,Piotr Polakowski,Jose A. Pitarque,Andrea Molinari,Małgorzata Rydzanicz,Bassem A. Bejjani,Jianbo Yue,Jacek P. Szaflik,Marzena Gajęcka	63

About Justyna A. Karolak

Justyna A. Karolak is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Molecular Biology, having authored 48 papers that have together received 771 indexed citations. Recurring topics across this work include Corneal surgery and disorders (17 papers), Corneal Surgery and Treatments (14 papers) and Renal and related cancers (10 papers). The work is most often cited by research in Ophthalmology (214 citations), Radiology, Nuclear Medicine and Imaging (412 citations) and Public Health, Environmental and Occupational Health (190 citations). Justyna A. Karolak has collaborated with scholars based in Poland, United States and Ecuador. Frequent co-authors include Marzena Gajęcka, Małgorzata Rydzanicz, Jacek P. Szaflik, Dorota Nowak, Paweł Stankiewicz, Piotr Polakowski, Tomasz Gambin, Jose A. Pitarque, Przemysław Szafrański and Michał Kabza. Their work appears in journals such as American Journal of Respiratory and Critical Care Medicine, Scientific Reports and Genome biology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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