Ben Pode‐Shakked

2.1k citations

55 papers · 670 · h-index 16

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Genetics
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders

Papers in

Molecular Biology 25
- Congenital heart defects research 4
- RNA regulation and disease 4
- Biochemical and Molecular Research 3
Genetics 14
- Connective tissue disorders research 5
- Genomics and Rare Diseases 5

Co-authors: Yair Anikster (29 shared papers)Ortal Barel (18 shared papers)Annick Raas‐Rothschild (20 shared papers)Asaf Vivante (9 shared papers)Naomi Pode‐Shakked (7 shared papers)Dina Marek‐Yagel (13 shared papers)Elon Pras (6 shared papers)Nechama Shalva (5 shared papers)
Journals: European Journal of Medical Genetics (9 papers)Pediatric Nephrology (3 papers)Clinical Genetics (3 papers)Frontiers in Genetics (3 papers)Molecular Genetics and Metabolism (3 papers)
Partner nations: Israel United States Türkiye

In The Last Decade

Ben Pode‐Shakked

51 papers receiving 656 citations

Peers

Countries citing papers authored by Ben Pode‐Shakked

Since Specialization

Citations

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

Fields of papers citing papers by Ben Pode‐Shakked

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ben Pode‐Shakked. 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 Ben Pode‐Shakked. The network helps show where Ben Pode‐Shakked may publish in the future.

Co-authors

The 25 scholars most cited alongside Ben Pode‐Shakked, 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 Ben Pode‐Shakked Line = papers co-authored together Ben Pode‐Shakked 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 55 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Dominant Negative Heterozygous G87R Mutation in the Zinc Transporter, ZnT-2 (SLC30A2), Results in Transient Neonatal Zinc Deficiency Journal of Biological Chemistry ·Inbal Lasry, Young Ah Seo, Hadas Ityel, Nechama Shalva, Ben Pode‐Shakked, Fabian Glaser, Bluma Berman, Igor N. Berezovsky, Alexander Goncearenco, Aharon Klar, Jacob Levy, Yair Anikster, Shannon L. Kelleher, Yehuda G. Assaraf	2012	80
2	Dissecting Stages of Human Kidney Development and Tumorigenesis with Surface Markers Affords Simple Prospective Purification of Nephron Stem Cells Scientific Reports ·Naomi Pode‐Shakked, Oren Pleniceanu, Rotem Gershon, Rachel Shukrun, Itamar Kanter, Efrat Bucris, Ben Pode‐Shakked, Gal Tam, Hadar Tam, Revital Caspi, Sara Pri‐Chen, Einav Vax, Guy Katz, Dorit Omer, Orit Harari‐Steinberg, Tomer Kalisky, Benjamin Dekel	2016	43
3	Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations European Journal of Human Genetics ·Joshi Stephen, Thierry Vilboux, Yael Haberman, Hadass Pri‐Chen, Ben Pode‐Shakked, Sina Mazaheri, Dina Marek‐Yagel, Ortal Barel, Ayelet Di Segni, Eran Eyal, Goni Hout‐Siloni, Avishay Lahad, Tzippora Shalem, Gideon Rechavi, May Christine V. Malicdan, Batia Weiss, William A. Gahl, Yair Anikster	2016	40
4	Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children Pediatric Nephrology ·Asaf Vivante, Orna Staretz Chacham, Shirlee Shril, Ruth Schreiber, Shrikant Mane, Ben Pode‐Shakked, Neveen A. Soliman, Irene Koneth, Mario Schiffer, Yair Anikster, Friedhelm Hildebrandt	2019	33
5	Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families Frontiers in Genetics ·Lior Greenbaum, Ben Pode‐Shakked, Shlomit Eisenberg‐Barzilai, Michal Dicastro-Keidar, Anat Bar-Ziv, Nurit Goldstein, Haike Reznik‐Wolf, Hana Poran, Amihai Rigbi, Ortal Barel, Aida M. Bertoli‐Avella, Peter Bauer, Miriam Regev, Annick Raas‐Rothschild, Elon Pras, Michal Berkenstadt	2019	32
6	Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases Pediatric Nephrology ·Asaf Vivante, Hadas Ityel, Ben Pode‐Shakked, Jing Chen, Shirlee Shril, Amelie T. van der Ven, Nina Mann, Johanna Magdalena Schmidt, Reeval Segel, Adi Aran, Avraham Zeharia, Orna Staretz‐Chacham, Omer Bar‐Yosef, Annick Raas‐Rothschild, Yuval E. Landau, Richard P. Lifton, Yair Anikster, (unknown)	2017	28
7	Expanding the molecular diversity and phenotypic spectrum of glycerol 3‐phosphate dehydrogenase 1 deficiency Journal of Inherited Metabolic Disease ·Carlo Dionisi‐Vici, Eyal Shteyer, Marcello Niceta, Cristiano Rizzo, Ben Pode‐Shakked, Giovanni Chillemi, Alessandro Bruselles, Michela Semeraro, Ortal Barel, Eran Eyal, Nitzan Kol, Yael Haberman, Avishai Lahad, Francesca Diomedi‐Camassei, Dina Marek‐Yagel, Gideon Rechavi, Marco Tartaglia, Yair Anikster	2016	25
8	Costeff syndrome: clinical features and natural history Journal of Neurology ·Gilad Yahalom, Yair Anikster, Ruth Huna-Baron, Chen Hoffmann, Lubov Blumkin, Dorit Lev, Rakefet Tsabari, Zeev Nitsan, Sheera F. Lerman, Bruria Ben‐Zeev, Ben Pode‐Shakked, Shira Sofer, Avraham Schweiger, Tally Lerman‐Sagie, Sharon Hassin‐Baer	2014	25
9	Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone‐mediated tubulinopathy Clinical Genetics ·Ben Pode‐Shakked, Hila Barash, Limor Ziv, Karen W. Gripp, Elisabetta Flex, Ortal Barel, Karinne Spirandelli Carvalho, Mena Scavina, Giovanni Chillemi, Marcello Niceta, Eran Eyal, Nitzan Kol, Bruria Ben‐Zeev, Omer Bar‐Yosef, Dina Marek‐Yagel, Enrico Bertini, Angela L. Duker, Yair Anikster, Marco Tartaglia, Annick Raas‐Rothschild	2016	23
10	BRPF1‐associated intellectual disability, ptosis, and facial dysmorphism in a multiplex family Molecular Genetics & Genomic Medicine ·Naomi Pode‐Shakked, Ortal Barel, Ben Pode‐Shakked, Aviva Eliyahu, Amihood Singer, Omri Nayshool, Nitzan Kol, Annick Raas‐Rothschild, Elon Pras, Mordechai Shohat	2019	22
11	Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome The American Journal of Human Genetics ·Asaf Ta‐Shma, Tahir Naeem Khan, Asaf Vivante, Jason R. Willer, Pavle Matak, Chaim Jalas, Ben Pode‐Shakked, Yishay Salem, Yair Anikster, Friedhelm Hildebrandt, Nicholas Katsanis, Orly Elpeleg, Erica E. Davis	2017	21
12	Prenatal diagnosis of 17q12 deletion syndrome: from fetal hyperechogenic kidneys to high risk for autism Prenatal Diagnosis ·Y. Gilboa, Sharon Perlman, Naomi Pode‐Shakked, Ben Pode‐Shakked, Alon Shrim, Einat Azaria-Lahav, Benjamin Dekel, Hagith Yonath, Michal Berkenstadt, R. Achiron	2016	21
13	Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia Human Genetics ·Ifat Bar-Joseph, Elon Pras, Haike Reznik‐Wolf, Dina Marek‐Yagel, Almogit Abu-Horvitz, Maya Dushnitzky, Nurit Goldstein, Shlomit Rienstein, Michal Dekel, Ben Pode‐Shakked, J Zlotnik, Anelia Benarrosh, Philippe Gillery, N Höfliger, Christiane Auray‐Blais, Roselyne Garnotel, Yair Anikster	2012	20
14	Man made disease: Clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse study Molecular Genetics and Metabolism ·Ben Pode‐Shakked, Lilach Shemer-Meiri, Alon Harmelin, Noa Stettner, Ori Brenner, Smadar Abraham, Gerard Schwartz, Yair Anikster	2013	19
15	The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase Deficiency Nutrients ·Orna Staretz‐Chacham, Ben Pode‐Shakked, Eyal Kristal, Smadar Abraham, Keren Porper, Ohad Wormser, Ilan Shelef, Yair Anikster	2021	17
16	Novel homozygous ENPP1 mutation causes generalized arterial calcifications of infancy, thrombocytopenia, and cardiovascular and central nervous system syndrome American Journal of Medical Genetics Part A ·Orna Staretz‐Chacham, Rachel Shukrun, Ortal Barel, Ben Pode‐Shakked, Oren Pleniceanu, Yair Anikster, Nechama Shalva, Carlos R. Ferreira, Admit Ben‐Haim Kadosh, Justin Richardson, Shrikant Mane, Friedhelm Hildebrandt, Asaf Vivante	2019	16
17	Clues and challenges in the diagnosis of intermittent maple syrup urine disease European Journal of Medical Genetics ·Naomi Pode‐Shakked, Stanley H. Korman, Ben Pode‐Shakked, Yuval E. Landau, Katya Kneller, Smadar Abraham, Avraham Shaag, Igor Ulanovsky, Suha Daas, Talya Saraf‐Levy, Haike Reznik‐Wolf, Asaf Vivante, Elon Pras, Shlomo Almashanu, Yair Anikster	2020	15
18	Bitterness of Glucose/Galactose Journal of Pediatric Gastroenterology and Nutrition ·Ben Pode‐Shakked, Orit Reish, Ayşe Çiğdem Aktuğlu Zeybek, Dafna Kesselman, Benjamin Dekel, Yoram Bujanover, Yair Anikster	2013	14
19	Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature BMC Medical Genetics ·Ben Pode‐Shakked, Asaf Vivante, Ortal Barel, Shai Padeh, Dina Marek‐Yagel, Alvit Veber, Shachar Abudi, Aviva Eliyahu, Irit Tirosh, Shiri Shpilman, Shirlee Shril, Friedhelm Hildebrandt, Mordechai Shohat, Yair Anikster	2019	13
20	Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay Frontiers in Pediatrics ·Aviva Eliyahu, Ortal Barel, Lior Greenbaum, Gal Zaks Hoffer, Yael Goldberg, Annick Raas‐Rothschild, Amihood Singer, Ifat Bar-Joseph, Vered Kunik, Elisheva Javasky, Orna Staretz‐Chacham, Naomi Pode‐Shakked, Lily Bazak, Noa Ruhrman‐Shahar, Elon Pras, Moshe Frydman, Mordechai Shohat, Ben Pode‐Shakked	2022	12

About Ben Pode‐Shakked

Ben Pode‐Shakked is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Biochemistry and Surgery, having authored 55 papers that have together received 670 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (7 papers), Lysosomal Storage Disorders Research (6 papers), Connective tissue disorders research (5 papers), Genomics and Rare Diseases (5 papers), Congenital heart defects research (4 papers), RNA regulation and disease (4 papers), Amino Acid Enzymes and Metabolism (4 papers) and Biochemical and Molecular Research (3 papers). The work is most often cited by research in Clinical Biochemistry (94 citations), Genetics (153 citations), Biochemistry (39 citations), Nutrition and Dietetics (79 citations) and Molecular Biology (303 citations). Ben Pode‐Shakked has collaborated with scholars based in Israel, United States and Türkiye. Frequent co-authors include Yair Anikster, Ortal Barel, Annick Raas‐Rothschild, Asaf Vivante, Naomi Pode‐Shakked, Dina Marek‐Yagel, Elon Pras, Nechama Shalva, Benjamin Dekel and Nitzan Kol. Their work appears in journals such as European Journal of Medical Genetics, Pediatric Nephrology, Clinical Genetics, Frontiers in Genetics and Molecular Genetics and Metabolism.

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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Ben Pode‐Shakked

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About Ben Pode‐Shakked

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