Eli Sprecher

16.0k citations

348 papers · 7.8k · h-index 47

Impact in

Cell Biology top 0.2%
- Skin and Cellular Biology Research
Dermatology top 0.2%
- Dermatology and Skin Diseases

Papers in

Cell Biology 134
- Skin and Cellular Biology Research 110
Molecular Biology 98
- Wnt/β-catenin signaling in development and cancer 33
- RNA regulation and disease 17

Co-authors: Ofer Sarig (81 shared papers)Margarita Indelman (31 shared papers)Yechiel Becker (19 shared papers)Gabriele Richard (20 shared papers)Liat Samuelov (50 shared papers)Jouni Uitto (18 shared papers)Orit Topaz (8 shared papers)Ilana Chefetz (8 shared papers)
Journals: Journal of Investigative Dermatology (43 papers)Clinical and Experimental Dermatology (36 papers)British Journal of Dermatology (32 papers)The American Journal of Human Genetics (14 papers)Journal of the American Academy of Dermatology (13 papers)
Partner nations: Israel United States Germany

In The Last Decade

Eli Sprecher

333 papers receiving 7.5k citations

Peers

Countries citing papers authored by Eli Sprecher

Since Specialization

Citations

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

Fields of papers citing papers by Eli Sprecher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Eli Sprecher, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eli Sprecher Line = papers co-authored together Eli Sprecher links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 348 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis Nature Genetics ·Orit Topaz, Daniel L. Shurman, (unknown), Margarita Indelman, Paulina Ratajczak, Mordechai Mizrachi, Ziad Khamaysi, Doron M. Behar, Dan Petronius, Vered Friedman, Israel Zelikovic, S. Raimer, Arieh Metzker, Gabriele Richard, Eli Sprecher	2004	473
2	SERKAL Syndrome: An Autosomal-Recessive Disorder Caused by a Loss-of-Function Mutation in WNT4 The American Journal of Human Genetics ·Hannah Mandel, Revital Shemer, Zvi Borochowitz, Marina Okopnik, Carlos Knopf, Margarita Indelman, Arie Drugan, Dov Tiosano, Ruth Gershoni‐Baruch, Mordechai Choder, Eli Sprecher	2008	191
3	Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14 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	2012	172
4	Autosomal Recessive Ichthyosis with Hypotrichosis Caused by a Mutation in ST14, Encoding Type II Transmembrane Serine Protease Matriptase The American Journal of Human Genetics ·Lina Basel‐Vanagaite, Revital Attia, Akemi Ishida‐Yamamoto, Limor Rainshtein, Dan Ben Amitai, Raziel Lurie, Metsada Pasmanik‐Chor, Margarita Indelman, Alex Zvulunov, Shirley Saban, Nurit Magal, Eli Sprecher, Mordechai Shohat	2007	148
5	A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma The American Journal of Human Genetics ·Eli Sprecher, Akemi Ishida‐Yamamoto, Mordechai Mizrahi-Koren, Debora Rapaport, Dorit Goldsher, Margarita Indelman, Orit Topaz, Ilana Chefetz, (unknown), Timothy J. O’Brien, Dani Bercovich, Stavit A. Shalev, Dan Geiger, (unknown), Mia Horowitz, Hanna Mandel	2005	143
6	Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin Nature Genetics ·Eli Sprecher, (unknown), Gabriele Richard, Raziel Lurie, Stavit A. Shalev, Dan Petronius, Adel Shalata, Yefim Anbinder, Rina Leibu, Ido Perlman, Nadine Cohen, Raymonde Szargel	2001	131
7	Association Between Vaccination With BNT162b2 and Incidence of Symptomatic and Asymptomatic SARS-CoV-2 Infections Among Health Care Workers JAMA ·Yoel Angel, Avishay Spitzer, Oryan Henig, Esther Saiag, Eli Sprecher, Hagit Padova, Ronen Ben‐Ami	2021	128
8	The Spectrum of Pathogenic Mutations in SPINK5 in 19 Families with Netherton Syndrome: Implications for Mutation Detection and First Case of Prenatal Diagnosis Journal of Investigative Dermatology ·Eli Sprecher, Shivan Amin, Karl Nielsen, Ellen G Pfendner, Jouni Uitto, Gabriele Richard, Stéphane Chavanas, John J. DiGiovanna, Julie Prendiville, Robert A. Silverman, Nancy B. Esterly, Mary K. Spraker, Ed Guelig, Margharita Larralde de Luna, Mary L. Williams, Bruce A. Buehler, Elaine C. Siegfried, Lionel Van Maldergem, Sherri J. Bale, Alain Hovnanian	2001	124
9	Desmoglein-1/Erbin interaction suppresses ERK activation to support epidermal differentiation Journal of Clinical Investigation ·Robert M. Harmon, Cory L. Simpson, Jodi Johnson, Jennifer L. Koetsier, Adi D. Dubash, Nicole A. Najor, Ofer Sarig, Eli Sprecher, Kathleen J. Green	2013	108
10	A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis The American Journal of Human Genetics ·Orit Topaz, Margarita Indelman, Ilana Chefetz, Dan Geiger, Aryeh Metzker, Yoram Altschuler, Mordechai Choder, Dani Bercovich, Jouni Uitto, (unknown), Gabriele Richard, Eli Sprecher	2006	106
11	A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification Human Genetics ·Ilana Chefetz, Raoul Heller, Assimina Galli‐Τsinopoulou, Gabriele Richard, Bernd Wollnik, Margarita Indelman, Friederike Koerber, Orit Topaz, (unknown), Eli Sprecher, Eckhard Schöenau	2005	101
12	Mechanisms Causing Loss of Keratinocyte Cohesion in Pemphigus Journal of Investigative Dermatology ·Volker Spindler, Rüdiger Eming, Enno Schmidt, Masayuki Amagai, Sergei A. Grando, Marcel F. Jonkman, Andrew P. Kowalczyk, Eliane J. Müller, Aimee Payne, Carlo Pincelli, Animesh A. Sinha, Eli Sprecher, Detlef Zillikens, Michael Hertl, Jens Waschke	2017	96
13	Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix Journal of Investigative Dermatology ·Eli Sprecher, Christopher J. Miller, Gabriele Richard, Akemi Ishida‐Yamamoto, Oren M. Becker, Lyuben N. Marekov, Peter M. Steinert, Kenneth H. Neldner	2001	93
14	Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders Journal of Molecular Medicine ·Yaacov Frishberg, Orit Topaz, (unknown), Doron M. Behar, Drora Fisher, Derek Gordon, Gabriele Richard, Eli Sprecher	2004	92
15	Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14 The American Journal of Human Genetics ·Jennie Lugassy, Peter Itin, Akemi Ishida‐Yamamoto, Kristen E. Holland, Susan Huson, Dan Geiger, Hans Christian Hennies, Margarita Indelman, Dani Bercovich, Jouni Uitto, (unknown), John A. McGrath, Gabriele Richard, Eli Sprecher	2006	91
16	Molecular Analysis of 250 Patients with Autosomal Recessive Congenital Ichthyosis: Evidence for Mutation Hotspots in ALOXE3 and Allelic Heterogeneity in ALOX12B Journal of Investigative Dermatology ·Katja‐Martina Eckl, Silvia de Juanes, Janine Kurtenbach, Marc Nätebus, Jenny Lugassy, Vinzenz Oji, Heiko Traupe, Marie-Luise Preil, Francisco Martı́nez, Josef Smolle, Avikam Harel, Peter Krieg, Eli Sprecher, Hans Christian Hennies	2009	86
17	Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin Journal of Allergy and Clinical Immunology ·Maeve A. McAleer, Elizabeth Pöhler, Frances J.D. Smith, Neil Wilson, Christian Cole, Stuart A. MacGowan, Jennifer L. Koetsier, Lisa M. Godsel, Robert M. Harmon, Robert Gruber, Debra Crumrine, Peter M. Elias, Michael McDermott, Karina Butler, Annemarie Broderick, Ofer Sarig, Eli Sprecher, Kathleen J. Green, W.H. Irwin McLean, Alan D. Irvine	2015	86
18	Effect of Aging on Epidermal Dendritic Cell Populations in C57BL/6J Mice Journal of Investigative Dermatology ·Eli Sprecher, Yechiel Becker, Georg Kraal, Elaine J. Hall, David G. Harrison, Leonard D. Shultz	1990	78
19	P-Cadherin Regulates Human Hair Growth and Cycling via Canonical Wnt Signaling and Transforming Growth Factor-β2 Journal of Investigative Dermatology ·Liat Samuelov, Eli Sprecher, Daisuke Tsuruta, Tamás Bı́ró, Jennifer E. Kloepper, Ralf Paus	2012	70
20	Proximity Ligation Assay for Detecting Protein‐Protein Interactions and Protein Modifications in Cells and Tissues in Situ Current Protocols in Cell Biology ·Marihan Hegazy, Eran Cohen‐Barak, Jennifer L. Koetsier, Nicole A. Najor, Constadina Arvanitis, Eli Sprecher, Kathleen J. Green, Lisa M. Godsel	2020	70

About Eli Sprecher

Eli Sprecher is a scholar working on Cell Biology, Molecular Biology, Dermatology, Genetics and Pathology and Forensic Medicine, having authored 348 papers that have together received 7.8k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (110 papers), Autoimmune Bullous Skin Diseases (38 papers), Hair Growth and Disorders (34 papers), Wnt/β-catenin signaling in development and cancer (33 papers), Genetic and rare skin diseases. (25 papers), Dermatological and Skeletal Disorders (19 papers), Immunotherapy and Immune Responses (17 papers) and RNA regulation and disease (17 papers). The work is most often cited by research in Cell Biology (2.3k citations), Dermatology (1.1k citations), Urology (723 citations), Nephrology (752 citations) and Genetics (1.5k citations). Eli Sprecher has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Ofer Sarig, Margarita Indelman, Yechiel Becker, Gabriele Richard, Liat Samuelov, Jouni Uitto, Orit Topaz, Ilana Chefetz, Akemi Ishida‐Yamamoto and Dana Fuchs‐Telem. Their work appears in journals such as Journal of Investigative Dermatology, Clinical and Experimental Dermatology, British Journal of Dermatology, The American Journal of Human Genetics and Journal of the American Academy of Dermatology.

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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Eli Sprecher

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