L Korniszewski

779 total citations
26 papers, 498 citations indexed

About

L Korniszewski is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, L Korniszewski has authored 26 papers receiving a total of 498 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 13 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in L Korniszewski's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). L Korniszewski is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). L Korniszewski collaborates with scholars based in Poland, United States and Belgium. L Korniszewski's co-authors include Rafał Płoski, Ralf Kist, Ken Dewar, Dietmar Pfeifer, Agnieszka Pollak, Agata Skórka, Bruce W. Birren, Eric S. Lander, Elke Back and Paweł Krajewski and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and European Respiratory Journal.

In The Last Decade

L Korniszewski

26 papers receiving 487 citations

Peers

Countries citing papers authored by L Korniszewski

Since Specialization

Citations

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

Fields of papers citing papers by L Korniszewski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Korniszewski

This figure shows the co-authorship network connecting the top 25 collaborators of L Korniszewski. A scholar is included among the top collaborators of L Korniszewski 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 L Korniszewski. L Korniszewski 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	Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability 2013 ·Journal of Applied Genetics ·Magdalena Bartnik, Beata Nowakowska, Katarzyna Derwińska, Barbara Wiśniowiecka‐Kowalnik, (unknown), (unknown), (unknown), Tomasz Gambin, Maciej Sykulski, (unknown), L Korniszewski, Anna Kutkowska‐Kaźmierczak, Jakub Klapecki, Krzysztof Szczałuba, Chad A. Shaw, Tadeusz Mazurczak, Anna Gambin, Ewa Obersztyn, Ewa Bocian, Paweł Stankiewicz	26
2	Postlingual Hearing Loss as a Mitochondrial 3243A>G Mutation Phenotype 2012 ·PLoS ONE ·Katarzyna Iwanicka‐Pronicka, Agnieszka Pollak, Agata Skórka, Urszula Lechowicz, Magdalena Pajdowska, Mariusz Furmanek, (unknown), L Korniszewski, Henryk Skarżyńśki, Rafał Płoski	16
3	MTHFR 677T Is a Strong Determinant of the Degree of Hearing Loss Among Polish Males with Postlingual Sensorineural Hearing Impairment 2012 ·DNA and Cell Biology ·Agnieszka Pollak, Małgorzata Mueller‐Malesińska, Urszula Lechowicz, Agata Skórka, L Korniszewski, (unknown), Anna Waśkiewicz, Grażyna Broda, Katarzyna Iwanicka‐Pronicka, Monika Ołdak, Henryk Skarżyńśki, Rafał Płoski	7
4	Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter 2011 ·American Journal of Medical Genetics Part A ·Piotr Iwanowski, Barbara Panasiuk, Griet Van Buggenhout, Marina Murdolo, M. Myśliwiec, Nicole Maas, Serena Lattante, L Korniszewski, Renata Posmyk, Jacek Pilch, Stanisław Zajączek, Jean‐Pierre Fryns, Marcella Zollino, Alina T. Midro	4
5	Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic features 2010 ·Journal of Applied Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Elżbieta Zdzienicka, L Korniszewski, Jacek Zaremba	4
6	Simple and translation forms of monosomy 4p16.1↔ pter: quantitative syndrome definition and cytogenetic evaluation by FISH 2007 ·Medizinische Genetik ·Alina T. Midro, (unknown), Barbara Panasiuk, Griet Van Buggenhout, (unknown), (unknown), Thomas Eggermann, Ján Pilch, L Korniszewski, Joris Vermeesch, Jean‐Pierre Fryns, Marcella Zollino	1
7	Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardation 2007 ·American Journal of Medical Genetics Part A ·Katarzyna Borg, Beata Nowakowska, Ewa Obersztyn, Sau Wai Cheung, (unknown), L Korniszewski, Tadeusz Mazurczak, Paweł Stankiewicz, Ewa Bocian	11
8	M34T and V37I mutations in GJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance 2007 ·American Journal of Medical Genetics Part A ·Agnieszka Pollak, Agata Skórka, Małgorzata Mueller‐Malesińska, Grażyna Kostrzewa, Bartłomiej Kisiel, (unknown), Paweł Krajewski, Monika Ołdak, L Korniszewski, Henryk Skarżyńśki, Rafał Płoski	85
9	Mild Smith-Lemli-Opitz syndrome: Further delineation of 5 Polish cases and review of the literature 2007 ·European Journal of Medical Genetics ·Aleksandra Jezela‐Stanek, Elżbieta Ciara, E Małunowicz, L Korniszewski, Dorota Piekutowska‐Abramczuk, Ewa Popowska, Małgorzata Krajewska‐Walasek	14
10	Molecular background of polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome in a Polish population: novel AIRE mutations and an estimate of disease prevalence 2006 ·Clinical Genetics ·Bartosz Stolarski, Ewa Pronicka, L Korniszewski, Agnieszka Pollak, Grażyna Kostrzewa, (unknown), Paweł Włodarski, Agata Skórka, (unknown), Paweł Krajewski, Rafał Płoski	49
11	CASE REPORT Leigh disease: 9 years follow up of a Polish family harboring T8993C mitochondrial DNA mutation 2005 ·Archives of Medical Science ·Bartłomiej Kisiel, L Korniszewski, Łukasz A. Małek	1
12	Fibular aplasia with ectrodactyly—broadening the clinical spectrum 2005 ·European Journal of Medical Genetics ·(unknown), Monika Ołdak, (unknown), (unknown), L Korniszewski	2
13	Fatal primary pulmonary hypertension in a 30‐yr-old female with APECED syndrome 2003 ·European Respiratory Journal ·L Korniszewski, Marcin Kurzyna, Bartosz Stolarski, Adam Torbicki, A Smerdel, Rafał Płoski	14
14	Two familial cases with a lethal gracile bone dysplasia and intrauterine growth retardation 2003 ·American Journal of Medical Genetics Part A ·L Korniszewski, Susan Arbuckle, K. Kozlowski	4
15	Increase in the Incidence of Type 1 Diabetes Mellitus in Children in Three Cities in Poland, 1987-1999 2002 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), L Korniszewski, (unknown)	8
16	Wiedemann-Rautenstrauch (neonatal progeroid) syndrome: New case with normal telomere length in skin fibroblasts 2001 ·American Journal of Medical Genetics ·L Korniszewski, (unknown), (unknown), (unknown), (unknown), (unknown)	21
17	Campomelic Dysplasia Translocation Breakpoints Are Scattered over 1 Mb Proximal to SOX9: Evidence for an Extended Control Region 1999 ·The American Journal of Human Genetics ·Dietmar Pfeifer, Ralf Kist, Ken Dewar, (unknown), Eric S. Lander, Bruce W. Birren, L Korniszewski, Elke Back, (unknown)	153
18	Supernumerary marker chromosomes characterized by fluorescence in situ hybridization (FISH) 1996 ·Journal of Applied Genetics ·Ewa Bocian, Paweł Stankiewicz, (unknown), Ewa Obersztyn, L Korniszewski, Tadeusz Mazurczak	1
19	The influence of vitamin E on rheological parameters in high altitude mountaineers. 1990 ·PubMed ·(unknown), L Korniszewski	21
20	[Wilms' tumor and Beckwith-Wiedemann syndrome]. 1985 ·PubMed ·(unknown), (unknown), L Korniszewski	2

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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