Dana Fuchs‐Telem

1.2k citations

20 papers · 728 indexed · h-index 15

Co-authors: Ofer Sarig Eli Sprecher Janna Nousbeck Shirli Israeli Ann Saada Jouni Uitto Shmuel Arnon Anne Lombès
Topics: Skin and Cellular Biology Research (8 papers)Wnt/β-catenin signaling in development and cancer (6 papers)Mesenchymal stem cell research (3 papers)
Cited by: Dermatology Cell Biology Clinical Biochemistry
Journals: Blood Scientific Reports The American Journal of Human Genetics
Partner nations: Israel United States Japan

In The Last Decade

Dana Fuchs‐Telem

20 papers receiving 713 citations

Peers

Countries citing papers authored by Dana Fuchs‐Telem

Since Specialization

Citations

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

Fields of papers citing papers by Dana Fuchs‐Telem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dana Fuchs‐Telem. 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 Dana Fuchs‐Telem. The network helps show where Dana Fuchs‐Telem may publish in the future.

Co-authorship network of co-authors of Dana Fuchs‐Telem

This figure shows the co-authorship network connecting the top 25 collaborators of Dana Fuchs‐Telem. A scholar is included among the top collaborators of Dana Fuchs‐Telem 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 Dana Fuchs‐Telem. Dana Fuchs‐Telem 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	Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis 2021 ·Experimental Dermatology ·Liat Samuelov,Ron Bochner,(unknown),(unknown),(unknown),Janna Nousbeck,Aviad Keren,Dana Fuchs‐Telem,Ofer Sarig,Amos Gilhar,Eli Sprecher	17
2	Human Placental-Derived Adherent Stromal Cells Co-Induced with TNF-α and IFN-γ Inhibit Triple-Negative Breast Cancer in Nude Mouse Xenograft Models 2018 ·Scientific Reports ·(unknown),Niva Shraga‐Heled,(unknown),(unknown),Dana Fuchs‐Telem,(unknown),Zami Aberman,Racheli Ofir	18
3	Human placental-derived adherent stromal cells co-induced with TNF-α and IFN-γ inhibit triple-negative breast cancer in nude mouse xenograft models 2018 ·Cytotherapy ·(unknown),Niva Shraga‐Heled,(unknown),(unknown),Dana Fuchs‐Telem,(unknown),Zami Aberman,Racheli Ofir	1
4	Intramuscular Administration of Placenta-Derived Stromal Cells Enhances Survival of Rhesus Macaque Monkeys Exposed to Total Body Irradiation 2017 ·Blood ·Noa Sher,(unknown),Dana Fuchs‐Telem,(unknown),Simon Authier,Polly Y. Chang,Alexis Ascah,James Bakke,Janet Gahagen,Racheli Ofir	1
5	Placenta-derived PLX-PAD mesenchymal-like stromal cells are efficacious in rescuing blood flow in hind limb ischemia mouse model by a dose- and site-dependent mechanism of action 2017 ·Cytotherapy ·(unknown),(unknown),Dana Fuchs‐Telem,Lena Pinzur,(unknown),Zami Aberman,Noa Sher,Racheli Ofir	28
6	RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR‐203 and p63 2015 ·Experimental Dermatology ·(unknown),Liat Samuelov,Ofer Sarig,Dan Vodo,Albrecht Bindereif,Moien Kanaan,Uri Gat,Dana Fuchs‐Telem,Noam Shomron,(unknown),Metsada Pasmanik‐Chor,(unknown),Eyal Winkler,(unknown),Isabelle Petit,Daniel Aberdam,Ralf Paus,Eli Sprecher,Janna Nousbeck	16
7	New intragenic and promoter region deletion mutations inFERMT1underscore genetic homogeneity in Kindler syndrome 2014 ·Clinical and Experimental Dermatology ·Dana Fuchs‐Telem,Janna Nousbeck,(unknown),John A. McGrath,Ofer Sarig,Eli Sprecher	12
8	Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site inKRT9 2013 ·Clinical and Experimental Dermatology ·Dana Fuchs‐Telem,Gilly Padalon‐Brauch,Ofer Sarig,Eli Sprecher	5
9	Cole Disease Results from Mutations in ENPP1 2013 ·The American Journal of Human Genetics ·Ori Eytan,Fanny Morice‐Picard,Ofer Sarig,Khaled Ezzedine,Ofer Isakov,Qiaoli Li,Akemi Ishida‐Yamamoto,Noam Shomron,(unknown),Dana Fuchs‐Telem,Noam Adir,Jouni Uitto,Seth J. Orlow,Alain Taı̈eb,Eli Sprecher	36
10	The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12 2013 ·Experimental Dermatology ·(unknown),Dana Fuchs‐Telem,Shirli Israeli,Ofer Sarig,Gilly Padalon‐Brauch,Richard N. Bergman,Margarita Indelman,Eli Sprecher,Janna Nousbeck	8
11	Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3‐Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh‐Like Syndrome) caused by novel mutations in SERAC1 2013 ·American Journal of Medical Genetics Part A ·Ofer Sarig,Dorit Goldsher,Janna Nousbeck,Dana Fuchs‐Telem,(unknown),Theodore C. Iancu,Irena Manov,Ann Saada,Eli Sprecher,Hanna Mandel	32
12	Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population 2013 ·Clinical and Experimental Dermatology ·Shirli Israeli,Ilan Goldberg,Dana Fuchs‐Telem,Richard N. Bergman,(unknown),(unknown),Avikam Harel,(unknown),Ofer Sarig,Eli Sprecher	29
13	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Syndrome Is Caused by a POC1A Mutation 2012 ·The American Journal of Human Genetics ·Ofer Sarig,(unknown),Debora Rapaport,Akemi Ishida‐Yamamoto,Dana Fuchs‐Telem,Qiaoli Li,(unknown),Ronen Spiegel,Janna Nousbeck,Shirli Israeli,(unknown),Gilly Padalon‐Brauch,Jouni Uitto,Mia Horowitz,Stavit A. Shalev,Eli Sprecher	53
14	Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14 2012 ·The American Journal of Human Genetics ·Dana Fuchs‐Telem,Ofer Sarig,Maurice A. M. Van Steensel,Ofer Isakov,Shirli Israeli,Janna Nousbeck,Katharina Richard,Véronique Winnepenninckx,Marigje Vernooij,Noam Shomron,Jouni Uitto,Philip Fleckman,Gabriele Richard,Eli Sprecher	161
15	A Mutation in a Skin-Specific Isoform of SMARCAD1 Causes Autosomal-Dominant Adermatoglyphia 2011 ·The American Journal of Human Genetics ·Janna Nousbeck,Bettina Burger,Dana Fuchs‐Telem,Mor Pavlovsky,(unknown),Ofer Sarig,Peter Itin,Eli Sprecher	32
16	Erythrokeratoderma variabilis caused by a recessive mutation in GJB3 2011 ·Clinical and Experimental Dermatology ·Dana Fuchs‐Telem,(unknown),B. Mevorah,Idit Shirazi,Ofer Sarig,Eli Sprecher	19
17	An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous family 2011 ·British Journal of Dermatology ·Liat Samuelov,Dana Fuchs‐Telem,Ofer Sarig,Eli Sprecher	17
18	A Mutation in LIPN, Encoding Epidermal Lipase N, Causes a Late-Onset Form of Autosomal-Recessive Congenital Ichthyosis 2011 ·The American Journal of Human Genetics ·Shirli Israeli,Ziad Khamaysi,Dana Fuchs‐Telem,Janna Nousbeck,Richard N. Bergman,Ofer Sarig,Eli Sprecher	53
19	CEDNIK syndrome results from loss-of-function mutations in SNAP29 2010 ·British Journal of Dermatology ·Dana Fuchs‐Telem,Helen Stewart,David Rapaport,Janna Nousbeck,Andrea Gat,(unknown),(unknown),Steffen Emmert,Katja‐Martina Eckl,(unknown),Ofer Sarig,Dorith Goldsher,(unknown),Akemi Ishida‐Yamamoto,Mia Horowitz,Eli Sprecher	64
20	Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation 2007 ·Journal of Medical Genetics ·Ann Saada,Avraham Shaag,Shmuel Arnon,T Dolfin,(unknown),Dana Fuchs‐Telem,Anne Lombès,Orly Elpeleg	126

About Dana Fuchs‐Telem

Dana Fuchs‐Telem is a scholar working on Cell Biology, Genetics and Molecular Biology, having authored 20 papers that have together received 728 indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (8 papers), Wnt/β-catenin signaling in development and cancer (6 papers) and Mesenchymal stem cell research (3 papers). The work is most often cited by research in Dermatology (110 citations), Cell Biology (197 citations) and Clinical Biochemistry (72 citations). Dana Fuchs‐Telem has collaborated with scholars based in Israel, United States and Japan. Frequent co-authors include Ofer Sarig, Eli Sprecher, Janna Nousbeck, Shirli Israeli, Ann Saada, Jouni Uitto, Shmuel Arnon, Anne Lombès, Orly Elpeleg and Avraham Shaag. Their work appears in journals such as Blood, Scientific Reports and The American Journal of Human Genetics.

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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