Ayala Frumkin

2.8k total citations · 1 hit paper
49 papers, 2.1k citations indexed

About

Ayala Frumkin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Ayala Frumkin has authored 49 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 23 papers in Pediatrics, Perinatology and Child Health and 16 papers in Molecular Biology. Recurrent topics in Ayala Frumkin's work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (14 papers) and Calcium signaling and nucleotide metabolism (8 papers). Ayala Frumkin is often cited by papers focused on Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (14 papers) and Calcium signaling and nucleotide metabolism (8 papers). Ayala Frumkin collaborates with scholars based in Israel, United States and Germany. Ayala Frumkin's co-authors include Gideon Bach, David A. Zeevi, Abraham Fainsod, Annick Raas‐Rothschild, Ruth Bargal, Tal Burstyn‐Cohen, Nili Avidan, Avihu Klar, Marcia Zeigler and Doron Lancet and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Nature Genetics.

In The Last Decade

Ayala Frumkin

48 papers receiving 2.0k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

1996 501 citations Ayala Frumkin et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ayala Frumkin Israel	22	1.1k	647	464	330	316	49	2.1k
Valérie Fraulob France	20	2.0k 1.8×	633 1.0×	53 0.1×	73 0.2×	90 0.3×	26	2.5k
Vasiliki Kalatzis France	27	1.3k 1.2×	390 0.6×	39 0.1×	214 0.6×	676 2.1×	69	2.6k
Yiqiang Cai United States	30	3.6k 3.4×	4.2k 6.4×	90 0.2×	335 1.0×	393 1.2×	63	5.5k
Arjan P.M. de Brouwer Netherlands	30	1.6k 1.5×	923 1.4×	28 0.1×	267 0.8×	130 0.4×	77	2.4k
Yoshiko Maeda Japan	18	1.4k 1.3×	1.3k 2.0×	46 0.1×	154 0.5×	117 0.4×	41	2.5k
Tamar Ben‐Yosef Israel	30	2.2k 2.0×	426 0.7×	31 0.1×	463 1.4×	60 0.2×	82	2.8k
Terry Watnick United States	41	3.5k 3.3×	4.2k 6.4×	47 0.1×	183 0.6×	514 1.6×	78	5.3k
Maria D. Lalioti United States	30	2.7k 2.5×	1.3k 2.0×	17 0.0×	72 0.2×	161 0.5×	56	4.7k
Elke De Vuyst Belgium	18	1.8k 1.6×	153 0.2×	81 0.2×	105 0.3×	26 0.1×	23	2.0k
Hammadi Ayadi Tunisia	29	1.3k 1.2×	673 1.0×	15 0.0×	792 2.4×	46 0.1×	137	2.6k

Countries citing papers authored by Ayala Frumkin

Since Specialization

Citations

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

Fields of papers citing papers by Ayala Frumkin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ayala Frumkin

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Slovik, Maya, Shamir Zenvirt, Ilana Livyatan, et al.. (2025). High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics. Clinical Genetics. 109(3). 529–538.

Frumkin, Ayala, et al.. (2022). CRISPR/Cas9-induced gene conversion between ATAD3 paralogs. Human Genetics and Genomics Advances. 3(2). 100092–100092. 2 indexed citations

Meiner, Vardiella, Simcha Yagel, Shamir Zenvirt, et al.. (2020). Universal chromosomal microarray analysis reveals high proportion of copy‐number variants in low‐risk pregnancies. Ultrasound in Obstetrics and Gynecology. 57(5). 813–820. 29 indexed citations

Singer, Amihood, et al.. (2019). Is fetal isolated double renal collecting system an indication for chromosomal microarray?. The Journal of Maternal-Fetal & Neonatal Medicine. 34(5). 696–700. 4 indexed citations

Sagi‐Dain, Lena, Idit Maya, Tzipora C. Falik‐Zaccai, et al.. (2018). Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray results. European Journal of Obstetrics & Gynecology and Reproductive Biology. 222. 80–83. 7 indexed citations

Daum, Hagit, Israela Lerer, Ayala Frumkin, et al.. (2018). Ultrasound findings provide clues to investigate founder mutations expressed as runs of homozygosity in chromosomal microarray studies. Prenatal Diagnosis. 38(2). 135–139. 8 indexed citations

Eventov‐Friedman, Smadar, Ayala Frumkin, Benjamin Bar‐Oz, & Annick Raas‐Rothschild. (2015). Mosaic Trisomy 14 in a Newborn with Multiple Malformations: When Chromosomal Microarray is a Clue to Diagnosis.. PubMed. 17(7). 459–60. 3 indexed citations

Cinnamon, Yuval, Yaacov Barak, Avraham Shaag, et al.. (2015). Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia. Journal of Assisted Reproduction and Genetics. 32(6). 887–891. 88 indexed citations

Ta‐Shma, Asaf, Zeev Perles, Yaacov Barak, et al.. (2014). A human laterality disorder associated with a homozygous WDR16 deletion. European Journal of Human Genetics. 23(9). 1262–1265. 35 indexed citations

10.

Sheffer, Ruth, Yaacov Barak, Simon Edvardson, et al.. (2014). Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A gene. Neurogenetics. 16(1). 23–26. 10 indexed citations

11.

Rump, Patrick, Nicole de Leeuw, Anthonie J. van Essen, et al.. (2014). Central 22q11.2 deletions. American Journal of Medical Genetics Part A. 164(11). 2707–2723. 43 indexed citations

12.

Edvardson, Simon, Vito Porcelli, Chaim Jalas, et al.. (2013). Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter. Journal of Medical Genetics. 50(4). 240–245. 53 indexed citations

13.

Michelson, Marina, Chana Vinkler, Esther Leshinsky‐Silver, et al.. (2012). Delineation of the interstitial 6q25 microdeletion syndrome: Refinement of the critical causative region. American Journal of Medical Genetics Part A. 158A(6). 1395–1399. 16 indexed citations

14.

Granot‐Hershkovitz, Einat, et al.. (2011). Complex chromosomal rearrangement in a girl with psychomotor‐retardation and a de novo inversion: inv(2)(p15;q24.2). American Journal of Medical Genetics Part A. 155(8). 1825–1832. 5 indexed citations

15.

Zeevi, David A., Shaya Lev, Ayala Frumkin, Baruch Minke, & Gideon Bach. (2010). Heteromultimeric TRPML channel assemblies play a crucial role in the regulation of cell viability models and starvation-induced autophagy. Journal of Cell Science. 123(18). 3112–3124. 50 indexed citations

16.

Bach, Gideon, David A. Zeevi, Ayala Frumkin, & Aviram Kogot‐Levin. (2010). Mucolipidosis type IV and the mucolipins. Biochemical Society Transactions. 38(6). 1432–1435. 17 indexed citations

17.

Lev, Shaya, et al.. (2009). Constitutive Activity of the Human TRPML2 Channel Induces Cell Degeneration. Journal of Biological Chemistry. 285(4). 2771–2782. 38 indexed citations

18.

Zeevi, David A., Ayala Frumkin, & Gideon Bach. (2007). TRPML and lysosomal function. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1772(8). 851–858. 69 indexed citations

19.

Yelin, Ronit, et al.. (2005). Ethanol exposure affects gene expression in the embryonic organizer and reduces retinoic acid levels. Developmental Biology. 279(1). 193–204. 92 indexed citations

20.

Bargal, Ruth, Nili Avidan, Edna Ben‐Asher, et al.. (2000). Identification of the gene causing mucolipidosis type IV. Nature Genetics. 26(1). 118–122. 305 indexed citations

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.

Explore authors with similar magnitude of impact