Alina Kurolap

1.8k total citations
42 papers, 399 citations indexed

About

Alina Kurolap is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Alina Kurolap has authored 42 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Alina Kurolap's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Mitochondrial Function and Pathology (6 papers). Alina Kurolap is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Mitochondrial Function and Pathology (6 papers). Alina Kurolap collaborates with scholars based in Israel, United States and Spain. Alina Kurolap's co-authors include Adi Mory, Hagit Baris Feldman, Ruth Gershoni‐Baruch, Efrat Dagan, Tova Hershkovitz, Tamar Paperna, Maria Nassar, Ilana Schlesinger, Hanna Mandel and Hagit Baris and has published in prestigious journals such as New England Journal of Medicine, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Alina Kurolap

37 papers receiving 395 citations

Peers

Countries citing papers authored by Alina Kurolap

Since Specialization

Citations

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

Fields of papers citing papers by Alina Kurolap

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alina Kurolap

This figure shows the co-authorship network connecting the top 25 collaborators of Alina Kurolap. A scholar is included among the top collaborators of Alina Kurolap 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 Alina Kurolap. Alina Kurolap 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	Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome 2025 ·Journal of Genetics ·Uri Hamiel, Alina Kurolap, (unknown), Adi Mory, Anat Bar Shira, Hagit Baris Feldman, Daphna Marom	0
2	Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening 2025 ·npj Digital Medicine ·Yuval Yaron, (unknown), Michal Berkenstadt, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Doron M. Behar, Elon Pras, Adi Reches, Alina Kurolap, Hagit Baris Feldman	0
3	PUF60 loss‐of‐function with normal cognition should be considered in the differential diagnosis of Klippel–Feil syndrome 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Alina Kurolap, Hagit Baris Feldman	0
4	SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance 2023 ·Prenatal Diagnosis ·(unknown), Alina Kurolap, Adi Mory, Karina Krajden Haratz, Dvora Kidron, G. Malinger, Hagit Baris Feldman, Yuval Yaron	3
5	A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescue 2023 ·Molecular Genetics and Metabolism ·Alina Kurolap, (unknown), (unknown), Isaiah D. Wexler, (unknown), Adi Mory, Ortal Barel, Shlomo Almashanu, Hagit Baris Feldman	1
6	Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharing 2022 ·Prenatal Diagnosis ·Alina Kurolap, Adi Mory, (unknown), Karina Krajden Haratz, G. Malinger, R. Birnbaum, Hagit Baris Feldman, Yuval Yaron	3
7	Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing 2022 ·Prenatal Diagnosis ·(unknown), (unknown), Yoav Yinon, (unknown), Alina Kurolap, Yuval Yaron, Hagit Baris Feldman	1
8	Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies 2022 ·Ultrasound in Obstetrics and Gynecology ·Yuval Yaron, (unknown), Adi Mory, (unknown), Alina Kurolap, Anat Bar Shira, (unknown), Daphna Marom, (unknown), Hagit Baris Feldman, G. Malinger, Karina Krajden Haratz, Adi Reches	48
9	Unique Ataxia-Oculomotor Apraxia 2 (AOA2) in Israel with Novel Variants, Atypical Late Presentation, and Possible Identification of a Poison Exon 2022 ·Journal of Molecular Neuroscience ·(unknown), Alina Kurolap, Israela Lerer, Judith Dagan, (unknown), Adi Mory, Yael Wilnai, (unknown), Nir Giladi, Tanya Gurevich, Vardiella Meiner, Alexander Lossos, Hagit Baris Feldman	2
10	CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a−) variant 2022 ·Human Genetics ·Alina Kurolap, David Hagin, Tal Freund, Sigal Fishman, (unknown), Eli Brazowski, Josepha Yeshaya, Tova Naiman, Elon Pras, Jacob N. Ablin, Hagit Baris Feldman	5
11	A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly 2021 ·American Journal of Medical Genetics Part A ·(unknown), Alina German, Amir Peleg, Claudia Gonzaga‐Jauregui, Tamar Paperna, Nina Ekhilevitch, Alina Kurolap, Hagit Baris Feldman, Lena Sagi‐Dain	0
12	A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4 2019 ·Journal of Human Genetics ·Tova Hershkovitz, Alina Kurolap, Claudia Gonzaga‐Jauregui, Tamar Paperna, Adi Mory, Sarah E. Wolf, John D. Overton, Alan R. Shuldiner, Ann Saada, Hanna Mandel, Hagit Baris Feldman	21
13	A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature 2019 ·American Journal of Medical Genetics Part A ·Lena Sagi‐Dain, Alina Kurolap, Anat Ilivitzki, Adi Mory, Tamar Paperna, (unknown), Claudia Gonzaga‐Jauregui, Amir Peleg, Hagit Baris Feldman	8
14	Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population 2019 ·European Journal of Medical Genetics ·Karin Weiss, Nina Ekhilevitch, Lior Cohen, (unknown), Rachel Bello, Ariel F. Martinez, Yarin Hadid, Liran I. Shlush, Alina Kurolap, Tamar Paperna, Adi Mory, Hagit Baris, Maximilian Muenke	6
15	Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine 2016 ·The American Journal of Human Genetics ·Alina Kurolap, (unknown), Tova Hershkovitz, (unknown), Adi Mory, Tamar Paperna, Ewald Hannappel, Galit Tal, (unknown), (unknown), Muhammad Mahajnah, Anat Ilivitzki, Dov Hershkovitz, Nina Ekhilevitch, Hanna Mandel, Volker Eulenburg, Hagit Baris	25
16	A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema 2015 ·Lymphatic Research and Biology ·(unknown), Alina Kurolap, Efrat Dagan, Adi Mory, Ruth Gershoni‐Baruch	8
17	The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews 2015 ·Parkinsonism & Related Disorders ·Efrat Dagan, Ilana Schlesinger, (unknown), Adi Mory, Maria Nassar, Alina Kurolap, (unknown), Ruth Gershoni‐Baruch	44
18	Kohlschutter-Tonz Syndrome: Clinical and Genetic Insights Gained From 16 Cases Deriving From a Close-Knit Village in Northern Israel 2014 ·Pediatric Neurology ·Adi Mory, Efrat Dagan, (unknown), Hanna Mandel, Barbara Illi, (unknown), Alina Kurolap, (unknown), Enza Maria Valente, Serge Amselem, Ruth Gershoni‐Baruch	16
19	“I Do Not Want My Baby to Suffer as I Did”; Prenatal and Preimplantation Genetic Diagnosis for BRCA1/2 Mutations: A Case Report and Genetic Counseling Considerations 2014 ·Genetic Testing and Molecular Biomarkers ·Efrat Dagan, Ruth Gershoni‐Baruch, Alina Kurolap, Yael Goldberg, Georgeta Fried	3
20	A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred 2013 ·European Journal of Human Genetics ·Adi Mory, Francesc X. Ruiz, Efrat Dagan, (unknown), Alina Kurolap, Xavier Parés, Jaume Farrés, Ruth Gershoni‐Baruch	22

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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