Dina Marek‐Yagel

2.5k citations

26 papers · 507 indexed · h-index 12

Co-authors: Haike Reznik‐Wolf Shai Padeh Avi Livneh Elon Pras Yackov Berkun Mordechai Pras Yair Anikster Ortal Barel
Topics: Mitochondrial Function and Pathology (5 papers)Metabolism and Genetic Disorders (4 papers)Amino Acid Enzymes and Metabolism (3 papers)
Cited by: Clinical Biochemistry Biochemistry Immunology
Journals: Digestive Diseases and Sciences Human Mutation Human Genetics
Partner nations: Israel United States Netherlands

In The Last Decade

Dina Marek‐Yagel

24 papers receiving 501 citations

Peers

Countries citing papers authored by Dina Marek‐Yagel

Since Specialization

Citations

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

Fields of papers citing papers by Dina Marek‐Yagel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dina Marek‐Yagel. 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 Dina Marek‐Yagel. The network helps show where Dina Marek‐Yagel may publish in the future.

Co-authorship network of co-authors of Dina Marek‐Yagel

This figure shows the co-authorship network connecting the top 25 collaborators of Dina Marek‐Yagel. A scholar is included among the top collaborators of Dina Marek‐Yagel 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 Dina Marek‐Yagel. Dina Marek‐Yagel 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	N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder 2025 ·European Journal of Human Genetics ·(unknown),Nurit Assia Batzir,(unknown),(unknown),Julián Nevado,Jair Tenorio,Pablo Lapunzina,(unknown),(unknown),(unknown),Sharon Aharoni,(unknown),Lina Basel‐Salmon,Naama Orenstein,Yakov Fellig,Shay Ben‐Shachar,Dina Marek‐Yagel,Víctor L. Ruiz‐Pérez	0
2	Biallelic MED29 variants cause pontocerebellar hypoplasia with cataracts 2025 ·European Journal of Human Genetics ·(unknown),Geeske M. van Woerden,Limor Ziv,Dina Marek‐Yagel,(unknown),(unknown),Ortal Barel,Nechama Shalva,(unknown),Yair Anikster,(unknown),(unknown),Shai Marcu,Andreea Nissenkorn,(unknown),Steven A. Kushner,Bruria Ben Zeev,Gali Heimer	0
3	Biallelic PIGM Coding Variant Causes Intractable Epilepsy and Intellectual Disability Without Thrombotic Events 2024 ·Clinical Genetics ·Gali Heimer,Ben Pode‐Shakked,Dina Marek‐Yagel,Helly Vernitsky,Michal Tzadok,Ortal Barel,Eran Eyal,Bruria Ben Zeev,Gil Atzmon,Yair Anikster	1
4	Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy 2022 ·Human Genetics ·Dina Marek‐Yagel,(unknown),Ben Pode‐Shakked,Cara Dunne,Ellen Crushell,(unknown),Michael McDermott,Maureen J. O’Sullivan,(unknown),Mansa Krishnamurthy,James M. Wells,Yair Anikster,Billy Bourke	1
5	Oculocutaneous albinism and bleeding diathesis due to a novel deletion in the HPS3 gene 2022 ·Frontiers in Genetics ·Dina Marek‐Yagel,(unknown),(unknown),(unknown),Nechama Shalva,(unknown),Ben Pode‐Shakked,May Christine V. Malicdan,Yair Anikster	2
6	Biallelic variants in ETV2 in a family with congenital heart defects, vertebral abnormalities and preaxial polydactyly 2021 ·European Journal of Medical Genetics ·Lina Basel‐Salmon,Noa Ruhrman‐Shahar,Ortal Barel,(unknown),Dina Marek‐Yagel,(unknown),Lily Bazak,Ran Svirsky,Haike Reznik‐Wolf,Gabriel Lidzbarsky,Mordechai Shohat	7
7	Four patients with D-bifunctional protein (DBP) deficiency: Expanding the phenotypic spectrum of a highly variable disease 2020 ·Molecular Genetics and Metabolism Reports ·Yuval E. Landau,Gali Heimer,Ortal Barel,Nechama Shalva,Dina Marek‐Yagel,(unknown),(unknown),(unknown),Andreea Nissenkorn,Bruria Ben‐Zeev,Yair Anikster	13
8	A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds 2020 ·American Journal of Medical Genetics Part A ·Dina Marek‐Yagel,(unknown),Ortal Barel,Amir Vardi,David Mishali,Uriel Katz,Yishay Salem,(unknown),(unknown),Nitzan Kol,Annick Raas‐Rothschild,Gideon Rechavi,Yair Anikster,Ben Pode‐Shakked	3
9	Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature 2019 ·BMC Medical Genetics ·Ben Pode‐Shakked,Asaf Vivante,Ortal Barel,Shai Padeh,Dina Marek‐Yagel,(unknown),(unknown),Aviva Eliyahu,Irit Tirosh,(unknown),Shirlee Shril,Friedhelm Hildebrandt,Mordechai Shohat,Yair Anikster	13
10	Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric Syndrome 2018 ·Digestive Diseases and Sciences ·(unknown),Ortal Barel,(unknown),Michael Schvimer,(unknown),Michael Field,Jodie Ouahed,Dina Marek‐Yagel,Lael Werner,Yael Haberman,Avishay Lahad,Yair Anikster,Gideon Rechavi,Iris Barshack,Joshua McElwee,Joseph Maranville,Raz Somech,Scott B. Snapper,Batia Weiss,Dror S. Shouval	8
11	Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin 2017 ·European Journal of Paediatric Neurology ·Gali Heimer,Eran Eyal,Xiaolin Zhu,Elizabeth K. Ruzzo,Dina Marek‐Yagel,Doron Sagiv,Yair Anikster,Haike Reznik‐Wolf,Eran Pras,(unknown),Doron Lancet,Bruria Ben‐Zeev,Andreea Nissenkorn	37
12	Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations 2016 ·European Journal of Human Genetics ·Joshi Stephen,Thierry Vilboux,Yael Haberman,(unknown),Ben Pode‐Shakked,(unknown),Dina Marek‐Yagel,Ortal Barel,Ayelet Di Segni,Eran Eyal,(unknown),Avishay Lahad,(unknown),Gideon Rechavi,May Christine V. Malicdan,Batia Weiss,William A. Gahl,Yair Anikster	34
13	Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone‐mediated tubulinopathy 2016 ·Clinical Genetics ·Ben Pode‐Shakked,Hila Barash,Limor Ziv,Karen W. Gripp,Elisabetta Flex,Ortal Barel,(unknown),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	22
14	A novel mutation in the C7orf11 gene causes nonphotosensitive trichothiodystrophy in a multiplex highly consanguineous kindred 2015 ·European Journal of Medical Genetics ·Ben Pode‐Shakked,Dina Marek‐Yagel,Shoshana Greenberger,Naomi Pode‐Shakked,Elon Pras,Aviv Barzilai,(unknown),Yechezkel Sidi,Yair Anikster	5
15	Glutaric Aciduria type I and acute renal failure — Coincidence or causality? 2014 ·Molecular Genetics and Metabolism Reports ·Ben Pode‐Shakked,Dina Marek‐Yagel,Marina Rubinshtein,Itai M. Pessach,Gideon Paret,Alexander Volkov,Yair Anikster,Danny Lotan	7
16	Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia 2012 ·Human Genetics ·Ifat Bar-Joseph,Elon Pras,Haike Reznik‐Wolf,Dina Marek‐Yagel,(unknown),(unknown),(unknown),Shlomit Rienstein,Michal Dekel,Ben Pode‐Shakked,(unknown),(unknown),Philippe Gillery,(unknown),Christiane Auray‐Blais,Roselyne Garnotel,Yair Anikster	18
17	X inactivation testing for identifying a non-syndromic X-linked mental retardation gene 2011 ·Journal of Applied Genetics ·Hagith Yonath,Dina Marek‐Yagel,(unknown),(unknown),Hagit Baris,Mordechai Shohat,Moshe Frydman,Elon Pras	4
18	Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean Fever 2010 ·Arthritis Care & Research ·Dina Marek‐Yagel,Yackov Berkun,Shai Padeh,Merav Lidar,Yael Shinar,Ifat Bar-Joseph,Haike Reznik‐Wolf,Pnina Langevitz,Avi Livneh,Elon Pras	13
19	A Novel Mutation in theHCN4Gene Causes Symptomatic Sinus Bradycardia in Moroccan Jews 2010 ·Journal of Cardiovascular Electrophysiology ·Avishag Laish‐Farkash,Michael Glikson,(unknown),Dina Marek‐Yagel,Elon Pras,Nathan Dascal,Charles Antzelevitch,Eyal Nof,(unknown),Michael Eldar,David Luria	47
20	Clinical disease among patients heterozygous for familial mediterranean fever 2009 ·Arthritis & Rheumatism ·Dina Marek‐Yagel,Yackov Berkun,Shai Padeh,(unknown),Haike Reznik‐Wolf,Avi Livneh,Mordechai Pras,Elon Pras	152

About Dina Marek‐Yagel

Dina Marek‐Yagel is a scholar working on Clinical Biochemistry, Biochemistry and Gastroenterology, having authored 26 papers that have together received 507 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). The work is most often cited by research in Clinical Biochemistry (63 citations), Biochemistry (50 citations) and Immunology (122 citations). Dina Marek‐Yagel has collaborated with scholars based in Israel, United States and Netherlands. Frequent co-authors include Haike Reznik‐Wolf, Shai Padeh, Avi Livneh, Elon Pras, Yackov Berkun, Mordechai Pras, Yair Anikster, Ortal Barel, Gali Heimer and Eran Eyal. Their work appears in journals such as Digestive Diseases and Sciences, Human Mutation and 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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