Karine Hovanes

2.9k total citations · 1 hit paper
28 papers, 1.9k citations indexed

About

Karine Hovanes is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karine Hovanes has authored 28 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karine Hovanes's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Karine Hovanes is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Karine Hovanes collaborates with scholars based in United States, Canada and Finland. Karine Hovanes's co-authors include Marian L. Waterman, Juha Paloneva, Tatjana Milovanović, Joan Marsh, Randall F. Holcombe, Jami Mandelin, Thomas D. Bird, Leena Peltonen, Tuula Manninen and Andrea Salmaggi and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Karine Hovanes

27 papers receiving 1.9k 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.

Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype

2002 522 citations Juha Paloneva, Tuula Manninen et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karine Hovanes United States	17	978	517	447	444	262	28	1.9k
Mordechai Shohat Israel	26	1.7k 1.7×	129 0.2×	237 0.5×	540 1.2×	432 1.6×	83	2.9k
Hammadi Ayadi Tunisia	29	1.3k 1.3×	298 0.6×	349 0.8×	673 1.5×	46 0.2×	137	2.6k
Mohammed Al‐Owain Saudi Arabia	25	1.1k 1.1×	356 0.7×	110 0.2×	595 1.3×	133 0.5×	87	2.0k
Sara Rollinson United Kingdom	28	847 0.9×	131 0.3×	336 0.8×	178 0.4×	81 0.3×	50	2.3k
David R. Witt United States	17	694 0.7×	146 0.3×	107 0.2×	444 1.0×	186 0.7×	23	1.9k
Chaim Jalas United States	23	724 0.7×	99 0.2×	127 0.3×	375 0.8×	475 1.8×	60	1.7k
Mirja Somer Finland	25	1.5k 1.5×	128 0.2×	141 0.3×	816 1.8×	240 0.9×	49	2.4k
Dong Hee Choi South Korea	24	652 0.7×	449 0.9×	268 0.6×	88 0.2×	409 1.6×	72	2.4k
Sharon Zeligson Israel	19	731 0.7×	96 0.2×	82 0.2×	281 0.6×	166 0.6×	41	1.3k
Cécile Cazeneuve France	24	975 1.0×	349 0.7×	212 0.5×	115 0.3×	49 0.2×	44	1.9k

Countries citing papers authored by Karine Hovanes

Since Specialization

Citations

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

Fields of papers citing papers by Karine Hovanes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karine Hovanes

This figure shows the co-authorship network connecting the top 25 collaborators of Karine Hovanes. A scholar is included among the top collaborators of Karine Hovanes 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 Karine Hovanes. Karine Hovanes 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

Meredith, Matthew M., Natasa Dzidic, Rima Slim, et al.. (2022). The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriages. Reproductive BioMedicine Online. 45(1). 125–134. 21 indexed citations

Dawson, Angelika J., Karine Hovanes, Jing Liu, et al.. (2020). Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly. Clinical Dysmorphology. 30(2). 83–88. 3 indexed citations

Sahoo, Trilochan, et al.. (2018). ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?. Prenatal Diagnosis. 38(3). 184–189. 53 indexed citations

Nguyen, Ngoc Minh, Zhao‐Jia Ge, Ramesh Reddy, et al.. (2018). Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles. The American Journal of Human Genetics. 103(5). 740–751. 62 indexed citations

Sahoo, Trilochan, Natasa Dzidic, Michelle N. Strecker, et al.. (2017). Comprehensive Genetic Analysis of Pregnancy Loss by Chromosomal Microarrays: Outcomes, Benefits, and Challenges. Obstetrical & Gynecological Survey. 72(5). 268–270. 3 indexed citations

Sahoo, Trilochan, Natasa Dzidic, Michelle N. Strecker, et al.. (2016). Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges. Genetics in Medicine. 19(1). 83–89. 120 indexed citations

Dawson, Angelika J., et al.. (2015). PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication. SHILAP Revista de lepidopterología. 2015. 1–3. 6 indexed citations

Dasouki, Majed, Jennifer Roberts, Angela Santiago, Irfan Saadi, & Karine Hovanes. (2014). Confirmation and further delineation of the 3q26.33–3q27.2 microdeletion syndrome. European Journal of Medical Genetics. 57(2-3). 76–80. 16 indexed citations

Roberts, Jennifer, Karine Hovanes, Majed Dasouki, Ann M. Manzardo, & Merlin G. Butler. (2013). Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services. Gene. 535(1). 70–78. 80 indexed citations

10.

Dasouki, Majed, et al.. (2011). The 3q29 microdeletion syndrome: Report of three new unrelated patients and in silico “RNA binding” analysis of the 3q29 region. American Journal of Medical Genetics Part A. 155(7). 1654–1660. 12 indexed citations

11.

Dawson, Angelika J., Ingo Schroedter, Matthew D. Seftel, et al.. (2011). Inversion and deletion of 16q22 defined by array CGH, FISH, and RT-PCR in a patient with AML. Cancer Genetics. 204(6). 344–347. 10 indexed citations

12.

Parker, Elizabeth, Karine Hovanes, John Germak, Forbes D. Porter, & Deborah P. Merke. (2006). Maternal 21‐hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21‐hydroxylase deficiency and Klinefelter syndrome. American Journal of Medical Genetics Part A. 140A(20). 2236–2240. 36 indexed citations

13.

Kiialainen, Anna, Karine Hovanes, Juha Paloneva, Outi Kopra, & Leena Peltonen. (2004). Dap12 and Trem2, molecules involved in innate immunity and neurodegeneration, are co-expressed in the CNS. Neurobiology of Disease. 18(2). 314–322. 91 indexed citations

14.

Li, Tony W.H., et al.. (2003). A New β-Catenin-dependent Activation Domain in T Cell Factor. Journal of Biological Chemistry. 278(18). 16169–16175. 67 indexed citations

15.

Paloneva, Juha, Tuula Manninen, Grant P. Christman, et al.. (2002). Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype. The American Journal of Human Genetics. 71(3). 656–662. 522 indexed citations breakdown →

16.

Hovanes, Karine, et al.. (2000). The human LEF-1 gene contains a promoter preferentially active in lymphocytes and encodes multiple isoforms derived from alternative splicing. Nucleic Acids Research. 28(9). 1994–2003. 84 indexed citations

17.

Dixon, Janet, Karine Hovanes, Rita Shiang, & Michael J. Dixon. (1997). Sequence Analysis, Identification of Evolutionary Conserved Motifs and Expression Analysis of Murine tcof1 Provide Further Evidence for a Potential Function for the Gene and Its Human Homologue, TCOF1. Human Molecular Genetics. 6(5). 727–737. 68 indexed citations

18.

Porfiri, Emilio, Bonnee Rubinfeld, Iris Albert, et al.. (1997). Induction of a β-catenin-LEF-1 complex by wnt-1 and transforming mutants of β-catenin. Oncogene. 15(23). 2833–2839. 133 indexed citations

19.

Douglas, Gordon C., Jinjie Hu, Twanda L. Thirkill, et al.. (1995). Cyclohexylamine inhibits the adhesion of lymphocytic cells to human syncytiotrophoblast. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1266(3). 229–234. 3 indexed citations

20.

Douglas, Gordon C., et al.. (1994). Effect of cytokines and anti-adhesion molecule antibodies on the adhesion of lymphocytic cells to human syncytiotrophoblast. Journal of Reproductive Immunology. 27(1). 49–62. 22 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.

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