Dorota Monies

5.2k total citations
48 papers, 1.3k citations indexed

About

Dorota Monies is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Dorota Monies has authored 48 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 24 papers in Molecular Biology and 8 papers in Immunology. Recurrent topics in Dorota Monies's work include Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Muscle Physiology and Disorders (4 papers). Dorota Monies is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Muscle Physiology and Disorders (4 papers). Dorota Monies collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Dorota Monies's co-authors include Brian F. Meyer, Mohamed Abouelhoda, Nada Al Tassan, Fowzan S. Alkuraya, Banan Al‐Younes, Mohamed El-Kalioby, Salma M. Wakil, Ewa Goljan, Saeed Bohlega and Jameela Shinwari and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Dorota Monies

48 papers receiving 1.2k citations

Peers

Countries citing papers authored by Dorota Monies

Since Specialization

Citations

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

Fields of papers citing papers by Dorota Monies

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorota Monies

This figure shows the co-authorship network connecting the top 25 collaborators of Dorota Monies. A scholar is included among the top collaborators of Dorota Monies 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 Dorota Monies. Dorota Monies 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	Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population 2024 ·Human Genomics ·Ewa Goljan, (unknown), Asma I. Tahir, Mohamed El-Kalioby, Brian F. Meyer, Dorota Monies	2
2	Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders 2023 ·Parkinsonism & Related Disorders ·Saeed Bohlega, (unknown), (unknown), Francisco J. Guzmán‐Vega, (unknown), (unknown), (unknown), (unknown), Dorota Monies, Stefan T. Arold	2
3	Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia 2022 ·Frontiers in Neuroscience ·(unknown), (unknown), Edward Cupler, Hindi Al‐Hindi, (unknown), (unknown), Dorota Monies, (unknown), (unknown), Brian F. Meyer, Saeed Bohlega	8
4	PLACK syndrome is potentially treatable with intralipids 2021 ·Clinical Genetics ·(unknown), Ali Almehaidib, Yousef Binamer, Dorota Monies, Khalid A. Alsaleem, Wajeeh Aldekhail, Fowzan S. Alkuraya, (unknown)	5
5	Molecular classification of blood and bleeding disorder genes 2021 ·npj Genomic Medicine ·Batoul Baz, Mohamed Abouelhoda, Tarek Owaidah, Majed Dasouki, Dorota Monies, Nada Al Tassan	2
6	Recessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification 2019 ·The American Journal of Human Genetics ·Dorota Monies, Cathrine Broberg Vågbø, Mohammad Al-Owain, (unknown), Fowzan S. Alkuraya	40
7	Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders 2019 ·Parkinsonism & Related Disorders ·Saeed Bohlega, Hussam Abou‐Al‐Shaar, (unknown), (unknown), (unknown), Brian F. Meyer, Dorota Monies, Edward Cupler, Amr Al‐Saif	20
8	Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients 2019 ·npj Genomic Medicine ·Tarek Owaidah, (unknown), Batoul Baz, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Nouf S. Al‐Numair, (unknown), (unknown), (unknown), Dorota Monies, (unknown), Nada Al Tassan	10
9	High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots 2018 ·Frontiers in Immunology ·Hamoud Al‐Mousa, (unknown), (unknown), (unknown), Mohamed Abouelhoda, (unknown), Dorota Monies, Brian F. Meyer, Abbas Hawwari, Majed Dasouki	54
10	De novo truncating variants in WHSC1 recapitulate the Wolf–Hirschhorn (4p16.3 microdeletion) syndrome phenotype 2018 ·Genetics in Medicine ·Nada Derar, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Dorota Monies, Mohamed Abouelhoda, Brian F. Meyer, Nabil Moghrabi, Fowzan S. Alkuraya	21
11	Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling 2018 ·BMC Medical Genetics ·(unknown), Minjing Zou, Roua A. Al‐Rijjal, Dorota Monies, Brian F. Meyer, Yufei Shi	1
12	Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families 2017 ·Scientific Reports ·Bashayer Al‐Mubarak, Mohamed Abouelhoda, (unknown), Hesham Aldhalaan, Mohammed S. Al‐Dosari, Michael Nester, (unknown), Mohamed El-Kalioby, Ewa Goljan, (unknown), Shazia Subhani, Asma I. Tahir, (unknown), (unknown), (unknown), (unknown), Jameela Shinwari, Dorota Monies, Nada Al Tassan	66
13	Genetic profiling of children with advanced cholestatic liver disease 2016 ·Clinical Genetics ·(unknown), John A. Burkholder, Dieter C. Bröering, Mohamed Abouelhoda, Tariq Faquih, Mohamed El-Kalioby, Shazia Subhani, Ewa Goljan, (unknown), Dorota Monies, Nejat Mazhar, (unknown), (unknown), Nada Al Tassan, Fowzan S. Alkuraya	30
14	Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden 2016 ·Genetics in Medicine ·Mohamed Abouelhoda, (unknown), Mohamed El-Kalioby, Nisha Patel, Hanan E. Shamseldin, Dorota Monies, Nada Al Tassan, Khushnooda Ramzan, Faiqa Imtiaz, Ranad Shaheen, Fowzan S. Alkuraya	67
15	Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract 2016 ·Human Genetics ·Nisha Patel, Deepti Anand, Dorota Monies, Sateesh Maddirevula, Arif O. Khan, Talal Algoufi, Mohammed Al‐Owain, Eissa Faqeih, Muneera Alshammari, (unknown), Hadeel Alsharif, (unknown), Hessa S. Alsaif, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, (unknown), Mohammed A. Aldahmesh, Salil A. Lachke, Fowzan S. Alkuraya	64
16	A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report 2016 ·BMC Neurology ·(unknown), Magdalena Badura‐Stronka, (unknown), (unknown), Barbara Steinborn, Anna Latos‐Bieleńska, Dorota Monies	28
17	A null mutation in TNIK defines a novel locus for intellectual disability 2016 ·Human Genetics ·Shams Anazi, Hanan E. Shamseldin, Dhekra Alnaqeb, Mohamed Abouelhoda, Dorota Monies, Mustafa A. Salih, Khalid Al‐Rubeaan, Fowzan S. Alkuraya	22
18	Exome-based case–control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy 2015 ·Human Genetics ·Corina Shtir, Mohammed A. Aldahmesh, Saad Al-Dahmash, Emad B. Abboud, Hisham Alkuraya, Marwan A. Abouammoh, (unknown), (unknown), (unknown), Banan Al‐Younes, (unknown), (unknown), (unknown), (unknown), Mais Hashem, Mohamed Abouelhoda, Dorota Monies, Fowzan S. Alkuraya	35
19	Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency 2014 ·PMC ·Ravikumar Balasubramanian, Jin‐Ho Choi, Ludmila Francescatto, Jason R. Willer, Edward R. Horton, (unknown), Konstantina M. Stanković, Lacey Plummer, Cassandra Buck, Richard Quinton, Todd D. Nebesio, Verónica Mericq, Paulina M. Merino, Brian F. Meyer, Dorota Monies, James F. Gusella, (unknown), Nicholas Katsanis, William F. Crowley	2
20	A novel deletion of theMEN1gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype 2011 ·Clinical Endocrinology ·Hussein Raef, Minjing Zou, Essa Y. Baitei, Roua A. Al‐Rijjal, Namik Kaya, Mohamed H. Al‐Hamed, Dorota Monies, (unknown), Hindi Al‐Hindi, Mohammed Hussien Alghamdi, Brian F. Meyer, Yufei Shi	29

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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