Paweł Stankiewicz

22.7k citations

198 papers · 9.2k indexed · 2 hit papers · h-index 50

Impact in

Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Molecular Biology top 1%
- Congenital heart defects research
- Genomics and Chromatin Dynamics
- Genomics and Phylogenetic Studies

Papers in

Genetics 137
- Genomic variations and chromosomal abnormalities 112
- Genomics and Rare Diseases 33
- Genetics and Neurodevelopmental Disorders 28
Developmental Biology 6

Co-authors: James R. Lupski Sau Wai Cheung Chad A. Shaw Arthur L. Beaudet Ankita Patel Przemysław Szafrański Ian M. Campbell Carlos A. Bacino
Journals: European Journal of Human Genetics (20 papers)Human Molecular Genetics (9 papers)Human Genetics (8 papers)The American Journal of Human Genetics (7 papers)Genome Research (7 papers)
Partner nations: United States Poland Germany

In The Last Decade

Paweł Stankiewicz

191 papers receiving 8.9k citations

Hit Papers

align trajectories log scale

Structural Variation in the Human Genome and its Role in Disease 2010 · 767 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2010 Annual Review of Medicine
2002 Trends in Genetics

Peers

Countries citing papers authored by Paweł Stankiewicz

Since Specialization

Citations

This map shows the geographic impact of Paweł Stankiewicz'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 Paweł Stankiewicz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paweł Stankiewicz more than expected).

Fields of papers citing papers by Paweł Stankiewicz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paweł Stankiewicz. 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 Paweł Stankiewicz. The network helps show where Paweł Stankiewicz may publish in the future.

Co-authors

The 25 scholars most cited alongside Paweł Stankiewicz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Paweł Stankiewicz Line = papers co-authored together Paweł Stankiewicz links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
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 Genome biology ·Barbara Poszewiecka, Krzysztof Gogolewski, Justyna A. Karolak, Paweł Stankiewicz, Anna Gambin	2023	2
2	Single Cell Multiomics Identifies Cells and Genetic Networks Underlying Alveolar Capillary Dysplasia American Journal of Respiratory and Critical Care Medicine ·Minzhe Guo, Kathryn A. Wikenheiser‐Brokamp, Joseph A. Kitzmiller, Cheng Jiang, 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, Jennifer Wambach, Jeffrey A. Whitsett	2023	14
3	Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis Genes ·Katarzyna Bzdęga, Anna Kutkowska‐Kaźmierczak, Gail Deutsch, Izabela Plaskota, Marta Smyk, Magdalena Niemiec, Artur Barczyk, Ewa Obersztyn, Jan Modzelewski, Iwona Lipska, Paweł Stankiewicz, Marzena Gajęcka, Małgorzata Rydzanicz, Rafał Płoski, Tomasz Szczapa, Justyna A. Karolak	2023	0
4	Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant European Journal of Human Genetics ·Esra Yıldız Bölükbaşı, Justyna A. Karolak, Przemysław Szafrański, Tomasz Gambin, Admire Matsika, Sam McManus, Hamish S. Scott, Peer Arts, Thuong Ha, Christopher Barnett, Jonathan Rodgers, Paweł Stankiewicz	2022	2
5	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 ·Esra Yıldız Bölükbaşı, Justyna A. Karolak, Przemysław Szafrański, Tomasz Gambin, Nicholas Willard, Steven H. Abman, Csaba Galambos, John P. Kinsella, Paweł Stankiewicz	2022	4
6	Genotype–phenotype correlation in two Polish neonates with alveolar capillary dysplasia BMC Pediatrics ·Zuzanna Kozłowska, Zuzanna Owsiańska, Joanna Wróblewska, Apolonia Kałużna, Andrzej Marszałek, Yogen Singh, Bartłomiej Mroziński, Qian Liu, Justyna A. Karolak, Paweł Stankiewicz, Gail Deutsch, Marta Szymankiewicz‐Bręborowicz, Tomasz Szczapa	2020	6
7	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 ·Justyna A. Karolak, Qian Liu, Nina Guanyi Xie, Lucia R. Wu, Gustavo Rocha, Susana Fernandes, Luk Ho-Ming, Ivan F. M. Lo, David Mowat, Elizabeth K. Fiorino, Morris Edelman, Joyce E. Fox, Denise A. Hayes, David P. Witte, Ashley Parrott, Edwina J. Popek, Przemysław Szafrański, David Y. Zhang, Paweł Stankiewicz	2020	12
8	Heterozygous CTNNB1 and TBX4 variants in a patient with abnormal lung growth, pulmonary hypertension, microcephaly, and spasticity Clinical Genetics ·Justyna A. Karolak, Przemysław Szafrański, David Kilner, Chirag Patel, Bonnie Scurry, Esther Kinning, Kate Chandler, Shalini N. Jhangiani, Zeynep H. Coban Akdemir, James R. Lupski, Edwina J. Popek, Paweł Stankiewicz	2019	12
9	Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation Molecular Genetics & Genomic Medicine ·Karin Salehi Karlslätt, Maria Pettersson, Nina Jäntti, Przemysław Szafrański, Tomas Wester, Britt Husberg, Ulla Ullberg, Paweł Stankiewicz, Ann Nordgren, Johanna Lundin, Anna Lindstrand, Agneta Nordenskjöld	2019	7
10	A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures American Journal of Medical Genetics Part A ·Marta Smyk, Elizabeth Roeder, Sau Wai Cheung, Przemysław Szafrański, Paweł Stankiewicz	2015	9
11	A stable density approach to probe selection for a custom aCGH design BioTechnologia ·Tomasz Gambin, Paweł Stankiewicz, Anna Gambin	2011	1
12	TGFBR2 deletion in a 20‐month‐old female with developmental delay and microcephaly American Journal of Medical Genetics Part A ·Ian M. Campbell, Katarzyna Kołodziejska, Michael Quach, Varina L. Wolf, Sau Wai Cheung, Seema R. Lalani, Melissa B. Ramocki, Paweł Stankiewicz	2011	13
13	Structural Variation in the Human Genome and its Role in Disease Annual Review of Medicine ·Paweł Stankiewicz, James R. Lupski Hit paper breakdown →	2010	767
14	Microduplication of Xp11.23p11.3 with effects on cognition, behavior, and craniofacial development Clinical Genetics ·AW El-Hattab, Juan C. Bournat, PA Eng, JBS Wu, BA Walker, Paweł Stankiewicz, SW Cheung, Chester Brown	2010	16
15	Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss European Journal of Human Genetics ·Sandesh C. Sreenath Nagamani, Ayelet Erez, Christine M. Eng, Zhishuo Ou, Craig Chinault, Laura A. Workman, James G. Coldwell, Paweł Stankiewicz, Ankita Patel, James R. Lupski, Sau Wai Cheung	2008	39
16	Genomic Disorders Humana Press eBooks ·James R. Lupski, Paweł Stankiewicz, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2006	21
17	Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease Human Molecular Genetics ·Jennifer A. Lee, Ken Inoue, Sau Wai Cheung, Chad A. Shaw, Paweł Stankiewicz, James R. Lupski	2006	56
18	Genomic disorders : the genomic basis of disease Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)) ·James R. Lupski, Paweł Stankiewicz	2006	51
19	Sotos syndrome common deletion is mediated by directly oriented subunits within inverted Sos-REP low-copy repeats Human Molecular Genetics ·Naohiro Kurotaki, Paweł Stankiewicz, Keiko Wakui, Norio Niikawa, James R. Lupski	2005	53
20	Supernumerary marker chromosomes characterized by fluorescence in situ hybridization (FISH) Journal of Applied Genetics ·Ewa Bocian, Paweł Stankiewicz, H. Stanczak, Ewa Obersztyn, L Korniszewski, Tadeusz Mazurczak	1996	1

About Paweł Stankiewicz

Paweł Stankiewicz is a scholar working on Genetics, Developmental Biology, Molecular Biology, Plant Science and Pediatrics, Perinatology and Child Health, having authored 198 papers that have together received 9.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (112 papers), Chromosomal and Genetic Variations (63 papers), Congenital heart defects research (39 papers), Genomics and Rare Diseases (33 papers), Genetics and Neurodevelopmental Disorders (28 papers), Prenatal Screening and Diagnostics (25 papers), RNA modifications and cancer (24 papers) and Renal and related cancers (21 papers). The work is most often cited by research in Genetics (6.2k citations), Molecular Biology (5.0k citations), Pediatrics, Perinatology and Child Health (1.4k citations), Plant Science (2.2k citations) and Developmental Biology (122 citations). Paweł Stankiewicz has collaborated with scholars based in United States, Poland and Germany. Frequent co-authors include James R. Lupski, Sau Wai Cheung, Chad A. Shaw, Arthur L. Beaudet, Ankita Patel, Przemysław Szafrański, Ian M. Campbell, Carlos A. Bacino, Weimin Bi and Seema R. Lalani. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, Human Genetics, The American Journal of Human Genetics and Genome Research.

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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