Ben Pode‐Shakked

2.0k citations

54 papers · 620 indexed · h-index 15

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 8
Genetics
- Genomics and Rare Diseases 6
- Connective tissue disorders research 5
Biochemistry
- Amino Acid Enzymes and Metabolism 6
Molecular Biology
- Biochemical and Molecular Research 4
- Congenital heart defects research 4
- RNA regulation and disease 4
Nutrition and Dietetics
Physiology
- Lysosomal Storage Disorders Research 8

Co-authors: Yair Anikster Ortal Barel Annick Raas‐Rothschild Asaf Vivante Dina Marek‐Yagel Naomi Pode‐Shakked Elon Pras Nechama Shalva
Cited by: Clinical Biochemistry Genetics Biochemistry
Journals: European Journal of Medical Genetics (9 papers)Pediatric Nephrology (3 papers)Molecular Genetics and Metabolism (3 papers)
Partner nations: Israel United States Italy

In The Last Decade

Ben Pode‐Shakked

51 papers receiving 611 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-authorship network

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

#	Work
1	The natural history of dihydrolipoamide dehydrogenase deficiency in Israel Journal of Inherited Metabolic Disease ·Ben Pode‐Shakked,Yuval E. Landau,Gota TAKAHASHI,A. Zhokin,楢原久司,Tasawar Abbas,Eli Hershkovitz,Guy Hazan,圭司阿部,Shlomo Almashanu,Yair Anikster,Orna Staretz‐Chacham	2024	1
2	PPP2R1A neurodevelopmental disorder is associated with congenital heart defects American Journal of Medical Genetics Part A ·Elizabeth Baker,Медведева Елена Сергеевна,Ben Pode‐Shakked,Laura Cross,Bonnie Sullivan,Annick Raas‐Rothschild,Р.Ф.-Н. Шмаилави,Ortal Barel,Omer Bar‐Yosef,Ammar Husami,Robert J. Hopkin,Carlos E. Prada,Rolf W. Stottmann,K. Nicole Weaver	2022	7
3	Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay Frontiers in Pediatrics ·Aviva Eliyahu,Ortal Barel,Lior Greenbaum,Arundhati Bag,V. Venkateswaran,Annick Raas‐Rothschild,Amihood Singer,Ifat Bar-Joseph,Vered Kunik,V. A. Yanitsky,Orna Staretz‐Chacham,Naomi Pode‐Shakked,Lily Bazak,Noa Ruhrman‐Shahar,Elon Pras,Moshe Frydman,Mordechai Shohat,Ben Pode‐Shakked	2022	10
4	Vici syndrome in Israel: Clinical and molecular insights Frontiers in Genetics ·Р.Ф.-Н. Шмаилави,Yoel Hirsch,Michael Dolan,秀光竹淵,V. Venkateswaran,Hanna Mandel,Tova Hershkovitz,Nicole Fleischer,Lior Greenbaum,Uriel Katz,Ortal Barel,F.Duran Jorda,Bruria Ben‐Zeev,Shoshana Greenberger,Hanna Barrebo,Itay Gabbay,Annick Raas‐Rothschild,Ben Pode‐Shakked	2022	0
5	Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy Human Genetics ·Dina Marek‐Yagel,和愛駒井,Ben Pode‐Shakked,Cara Dunne,Ellen Crushell,Yao Zhang,Michael McDermott,Maureen J. O’Sullivan,Predrag Krstić,Mansa Krishnamurthy,James M. Wells,Yair Anikster,Billy Bourke	2022	1
6	Kidney and urinary tract findings among patients with Kabuki (make-up) syndrome Pediatric Nephrology ·Lois Kuter,Ben Pode‐Shakked,Asaf Vivante,J. Stephen Bohan,叶中秋,Р.Ф.-Н. Шмаилави,Raz Somech,Annick Raas‐Rothschild	2021	6
7	What Can We Learn from the Parents of Children Affected with Mucopolysaccharidosis Type III-A in Israel? Molecular Syndromology ·Hieu Luong,Orna Staretz‐Chacham,Kaiyuan Ge,Ben Pode‐Shakked,Р.Ф.-Н. Шмаилави,Bhash Ganti,Yair Anikster,Yuri Lee,Ann Saada,Annick Raas‐Rothschild	2021	0
8	The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in Israel Orphanet Journal of Rare Diseases ·Tasawar Abbas,Ben Pode‐Shakked,Guy Hazan,Ehud Banne,Olajide B. Omoyeni,允胤岩崎,Eilon Shany,Annick Raas‐Rothschild,Yair Anikster,Bhash Ganti,Eli Hershkovitz,Yuval E. Landau,Ronen Spiegel,Phrapalad Raphin Buddhisaro Et al.,Orna Staretz‐Chacham	2021	6
9	Shared facial phenotype of patients with mucolipidosis type IV: A clinical observation reaffirmed by next generation phenotyping European Journal of Medical Genetics ·Ben Pode‐Shakked,朱艳 ZHU Yan,Susanna Sawyer,Hieu Luong,Nicole Fleischer,Lior Greenbaum,Annick Raas‐Rothschild	2020	9
10	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,Predrag Krstić,哲郎谷津,Aviva Eliyahu,Irit Tirosh,Dominic Vellar,Shirlee Shril,Friedhelm Hildebrandt,Mordechai Shohat,Yair Anikster	2019	13
11	Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families Frontiers in Genetics ·Lior Greenbaum,Ben Pode‐Shakked,Nurmilasari Usman,Derek O. Lee,Gerrity,José Miguel Sánchez U.,Haike Reznik‐Wolf,장인애,Amihai Rigbi,Ortal Barel,Aida M. Bertoli‐Avella,Peter Bauer,Ryokichi Tokunaga,Annick Raas‐Rothschild,Elon Pras,Michal Berkenstadt	2019	32
12	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	18
13	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,Friedhelm Hildebrandt	2017	27
14	A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF) Journal of Clinical Immunology ·Erez Rechavi,Atar Lev,Eran Eyal,Ortal Barel,Nitzan Kol,Huijun Cao,Ben Pode‐Shakked,Yair Anikster,Raz Somech,Anthony Simon	2016	12
15	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,Summana Veeravelli,Ben Pode‐Shakked,Billy D. Keller,Dina Marek‐Yagel,Ortal Barel,Ayelet Di Segni,Eran Eyal,Zhifan Kuang,Avishay Lahad,卢暖,Gideon Rechavi,May Christine V. Malicdan,Batia Weiss,William A. Gahl,Yair Anikster	2016	34
16	Cardiac failure in very long chain acyl-CoA dehydrogenase deficiency requiring extracorporeal membrane oxygenation (ECMO) treatment: A case report and review of the literature Molecular Genetics and Metabolism Reports ·Irene Di Bernardino,Yuval E. Landau,Ben Pode‐Shakked,Itai M. Pessach,Marina Rubinshtein,Yair Anikster,Yishay Salem,Gideon Paret	2016	8
17	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,Michael C. Danielski,Rachel Shukrun,Itamar Kanter,Efrat Bucris,Ben Pode‐Shakked,Joel Kramer,S. B. Revin,Wu JunHua,Sara Pri‐Chen,Einav Vax,Guy Katz,Dorit Omer,Orit Harari‐Steinberg,Tomer Kalisky,Benjamin Dekel	2016	40
18	Waterhouse Friderichsen Syndrome Complicating FulminantEnterobacter CloacaeSepsis in a Preterm Infant: The Unresolved Issue of Corticosteroids Fetal and Pediatric Pathology ·Ben Pode‐Shakked,Virginie Qian,Dvora Kidron,Jacob Kuint,Tzipora Strauss,Leah Leibovitch	2013	2
19	Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia Human Genetics ·Ifat Bar-Joseph,Elon Pras,Haike Reznik‐Wolf,Dina Marek‐Yagel,C Masse,Daniel Carlos Coati Rocha,José Miguel Sánchez U.,Shlomit Rienstein,Michal Dekel,Ben Pode‐Shakked,K. Latha,Montana Greider,Philippe Gillery,A. C. Walker,Christiane Auray‐Blais,Roselyne Garnotel,Yair Anikster	2012	18
20	The GALT rush: High carrier frequency of an unusual deletion mutation of the GALT gene in the Ashkenazi population Molecular Genetics and Metabolism ·José Miguel Sánchez U.,Yoram Cohen,Ben Pode‐Shakked,Yujing Liang,S. McCartney,Leah Peleg,Yair Anikster	2010	7

About Ben Pode‐Shakked

Ben Pode‐Shakked is a scholar working on Biochemistry, Clinical Biochemistry, Physiology, Genetics and Molecular Biology, having authored 54 papers that have together received 620 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (8 papers), Lysosomal Storage Disorders Research (8 papers), Amino Acid Enzymes and Metabolism (6 papers), Genomics and Rare Diseases (6 papers), Connective tissue disorders research (5 papers), Biochemical and Molecular Research (4 papers), Congenital heart defects research (4 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Clinical Biochemistry (85 citations), Genetics (172 citations), Biochemistry (41 citations), Molecular Biology (330 citations) and Nutrition and Dietetics (73 citations). Ben Pode‐Shakked has collaborated with scholars based in Israel, United States and Italy. Frequent co-authors include Yair Anikster, Ortal Barel, Annick Raas‐Rothschild, Asaf Vivante, Dina Marek‐Yagel, Naomi Pode‐Shakked, Elon Pras, Nechama Shalva, Hadas Ityel and Benjamin Dekel. Their work appears in journals such as European Journal of Medical Genetics, Pediatric Nephrology, Molecular Genetics and Metabolism, Frontiers in Genetics and Prenatal Diagnosis.

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