Josepha Yeshaya

643 total citations
18 papers, 455 citations indexed

About

Josepha Yeshaya is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Josepha Yeshaya has authored 18 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Josepha Yeshaya's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Congenital heart defects research (4 papers). Josepha Yeshaya is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Congenital heart defects research (4 papers). Josepha Yeshaya collaborates with scholars based in Israel and United States. Josepha Yeshaya's co-authors include Mordechai Shohat, Idit Maya, Sarit Kahana, Lina Basel‐Vanagaite, Shiri Yacobson, Reuven Sharony, Tamar Tenne, Merav Burg, Ada H. Zohar and Abraham Weizman and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

Josepha Yeshaya

18 papers receiving 423 citations

Peers

Countries citing papers authored by Josepha Yeshaya

Since Specialization

Citations

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

Fields of papers citing papers by Josepha Yeshaya

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josepha Yeshaya

This figure shows the co-authorship network connecting the top 25 collaborators of Josepha Yeshaya. A scholar is included among the top collaborators of Josepha Yeshaya 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 Josepha Yeshaya. Josepha Yeshaya is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Expanded targeted preconception screening panel in Israel: findings and insights 2024 ·Journal of Medical Genetics ·Adi Reches, (unknown), (unknown), Josepha Yeshaya, (unknown), (unknown), T.E. Hallas, (unknown), Alina Kurolap, Michal Berkenstadt, (unknown), (unknown), (unknown), Haike Reznik‐Wolf, Doron M. Behar, Yuval Yaron, Elon Pras, Hagit Baris Feldman	3
2	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
3	When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations 2017 ·Genetics in Medicine ·Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, (unknown), (unknown), Yael Goldberg, (unknown), Lina Basel‐Salmon, Mordechai Shohat	46
4	Cut‐off value of nuchal translucency as indication for chromosomal microarray analysis 2017 ·Ultrasound in Obstetrics and Gynecology ·Idit Maya, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, (unknown), (unknown), M Shohat, Lina Basel‐Vanagaite, Reuven Sharony	46
5	Cytogenetic analysis in fetuses with late onset abnormal sonographic findings 2017 ·Journal of Perinatal Medicine ·Ron Bardin, Eran Hadar, (unknown), Rinat Gabbay‐Benziv, Israel Meizner, Sarit Kahana, Josepha Yeshaya, Shiri Yacobson, (unknown), (unknown), Lina Basel‐Vanagaite, Idit Maya	15
6	Chromosomal microarray analysis in fetuses with aberrant right subclavian artery 2016 ·Ultrasound in Obstetrics and Gynecology ·Idit Maya, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Shiri Yacobson, (unknown), (unknown), (unknown), Eyal Reinstein, Lina Basel‐Vanagaite, Reuven Sharony	36
7	A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysis 2015 ·European Journal of Paediatric Neurology ·Aviva Mimouni-Bloch, Josepha Yeshaya, Sarit Kahana, Idit Maya, Lina Basel‐Vanagaite	27
8	Acute promyelocytic leukemia with isochromosome 17q and cryptic PML-RARA successfully treated with all-trans retinoic acid and arsenic trioxide 2015 ·Cancer Genetics ·Daniel Shepshelovich, (unknown), (unknown), Alina Klein, Eli Muchtar, Josepha Yeshaya, Adina Aviram, Esther Rabizadeh, Pia Raanani	10
9	Abnormal brain magnetic resonance imaging in two patients with Smith–Magenis syndrome 2014 ·American Journal of Medical Genetics Part A ·Idit Maya, Chana Vinkler, Osnat Konen, Liora Kornreich, Tamar Steinberg, Josepha Yeshaya, (unknown), Mordechai Shohat, Dorit Lev, Hagit Baris	23
10	Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA 2009 ·Molecular Cytogenetics ·Josepha Yeshaya, (unknown), (unknown), Jane E. Freedman, Mordechai Shohat, Lydia Avivi	6
11	On the Classification of a Small Imbalanced Cytogenetic Image Database 2007 ·IEEE/ACM Transactions on Computational Biology and Bioinformatics ·Boaz Lerner, Josepha Yeshaya, (unknown)	16
12	Segmentation and Classification of Dot and Non-Dot-Like Fluorescencein situHybridization Signals for Automated Detection of Cytogenetic Abnormalities 2007 ·IEEE Transactions on Information Technology in Biomedicine ·Boaz Lerner, (unknown), Josepha Yeshaya	10
13	Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome 2006 ·The International Journal of Neuropsychopharmacology ·Doron Gothelf, Elena Michaelovsky, Amos Frisch, Ada H. Zohar, (unknown), Merav Burg, Ayala Aviram‐Goldring, Moshe Frydman, Josepha Yeshaya, Mordechai Shohat, Michael Korostishevsky, Alan Apter, Abraham Weizman	55
14	Obsessive‐compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome 2003 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Doron Gothelf, (unknown), Ada H. Zohar, Merav Burg, (unknown), Moshe Frydman, Mordechai Shohat, Dov Inbar, Ayala Aviram‐Goldring, Josepha Yeshaya, Tamar Steinberg, Yehuda Finkelstein, Amos Frisch, Abraham Weizman, Alan Apter	114
15	Phenotypic expression of tissue mosaicism in a 45,X/46,X,dicY(q11.2) female 2001 ·American Journal of Medical Genetics ·(unknown), Arieh Kauschansky, Josepha Yeshaya, Jane E. Freedman, Uriel Barkai, Ana Tobar, Elimelech Okon, (unknown), Mordechai Shohat, Cyril Legum	6
16	FISH-detected delay in replication timing of mutated FMR1 alleles on both active and inactive X-chromosomes 1999 ·Human Genetics ·Josepha Yeshaya, R. Shalgi, Mordechai Shohat, Lydia Avivi	16
17	FISH-detected delay in replication timing of mutated FMR1 alleles on both active and inactive X-chromosomes 1999 ·Human Genetics ·Josepha Yeshaya, (unknown), (unknown), Lydia Avivi	5
18	Replication timing of the various FMR1 alleles detected by FISH: inferences regarding their transcriptional status 1998 ·Human Genetics ·Josepha Yeshaya, R. Shalgi, Mordechai Shohat, Lydia Avivi	16

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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