Małgorzata Rydzanicz

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 10 papers. Top paper: “Variants in FLRT3 and SLC35E2B identified using exome sequencing in seven high myopia families from Central Europe”.

Variants in FLRT3 and SLC35E2B identified using exome sequencing in seven high myopia families from Central Europe

Advances in Medical Sciences(2021)10.1016/j.advms.2021.02.005

N/A

0DataRank · unranked

8 citations

Justyna A. Karolak, Tomasz Gambin, Małgorzata Rydzanicz, Agata Frajdenberg, Małgorzata Mrugacz +5 more

TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.10.007

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0DataRank · unranked

26 citations

Linda M. Reis, Davut Pehli̇van, Jonathan A. Bernstein, Michael Muriello, Erin Syverson +33 more

Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype–phenotype correlation study

Genetics in Medicine(2022)10.1016/j.gim.2022.09.007

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0DataRank · unranked

11 citations

Agostina Tardivo, Alexej Knaus, Mona Hashim, Alistair T. Pagnamenta, Kerstin Alt +39 more

A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia

Human Molecular Genetics(2022)10.1093/hmg/ddac276

N/A

0DataRank · unranked

2 citations

Magdalena Krygier, Natalia A. Szulc, Karolina Rutkowska, Joanna Kosińska, Agnieszka Pollak +6 more

A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs, and limb ataxia

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.24.489208

N/A

0DataRank · unranked

0 citations

Magdalena Krygier, Natalia A. Szulc, Karolina Rutkowska, Joanna Kosińska, Agnieszka Pollak +6 more

Long read sequencing identifies complex structural variant landscape and recurrent TERT rearrangements in mucoepidermoid carcinoma

Oral Oncology(2024)10.1016/j.oraloncology.2024.107108

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0DataRank · unranked

4 citations

Apurva D. Bhangale, Dana Al Majid, Victor Murcia Pienkowski, Małgorzata Rydzanicz, Joanna Janiszewska +16 more

Epigenomic and phenotypic characterization of DEGCAGS syndrome

European Journal of Human Genetics(2024)10.1038/s41431-024-01702-y

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0DataRank · unranked

6 citations

Denisa Weis, Ingvild Aukrust, Tzung‐Chien Hsieh, Marie Horackova, Julie Paulsen +37 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369

N/A

0DataRank · unranked

4 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 more

CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies

Science Advances(2025)10.1126/sciadv.adw3717

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0DataRank · unranked

1 citations

Erika Tavares, Katherine Bishara, Ayşegül Ozantürk, Leila Qebibo, Stephan Frangakis +25 more

A novel MAPK1 variant in a family with complex psychiatric and neurodegenerative clinical phenotype

Research Square(2025)10.21203/rs.3.rs-5881666/v1

N/A

0DataRank · unranked

0 citations

Abhishek Anil Dubey, Małgorzata Rydzanicz, Anna Barczak, Natalia Szulc, Bartłomiej Surpeta +14 more