Haike Reznik‐Wolf

1.7k total citations
39 papers, 888 citations indexed

About

Haike Reznik‐Wolf is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Haike Reznik‐Wolf has authored 39 papers receiving a total of 888 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Haike Reznik‐Wolf's work include Metabolism and Genetic Disorders (4 papers), Connective tissue disorders research (4 papers) and Hereditary Neurological Disorders (4 papers). Haike Reznik‐Wolf is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Connective tissue disorders research (4 papers) and Hereditary Neurological Disorders (4 papers). Haike Reznik‐Wolf collaborates with scholars based in Israel, United States and Germany. Haike Reznik‐Wolf's co-authors include Elon Pras, Eran Pras, Dina Marek‐Yagel, Moshe Frydman, Avi Livneh, Elon Pras, Yackov Berkun, Shai Padeh, Mordechai Pras and Uri Nir and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Haike Reznik‐Wolf

37 papers receiving 875 citations

Peers

Countries citing papers authored by Haike Reznik‐Wolf

Since Specialization

Citations

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

Fields of papers citing papers by Haike Reznik‐Wolf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Haike Reznik‐Wolf. 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 Haike Reznik‐Wolf. The network helps show where Haike Reznik‐Wolf may publish in the future.

Co-authorship network of co-authors of Haike Reznik‐Wolf

This figure shows the co-authorship network connecting the top 25 collaborators of Haike Reznik‐Wolf. A scholar is included among the top collaborators of Haike Reznik‐Wolf 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 Haike Reznik‐Wolf. Haike Reznik‐Wolf 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

#	Title	Journal	Authors	Indexed citations
1	Biallelic variants in ETV2 in a family with congenital heart defects, vertebral abnormalities and preaxial polydactyly	European Journal of Medical Genetics	Lina Basel‐Salmon, Noa Ruhrman‐Shahar et al.	7
2	Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi Jews	International Journal of Cardiology	Shimrit Oz, Hagith Yonath et al.	11
3	Clues and challenges in the diagnosis of intermittent maple syrup urine disease	European Journal of Medical Genetics	Naomi Pode‐Shakked, Stanley H. Korman et al.	13
4	Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families	Frontiers in Genetics	Lior Greenbaum, Ben Pode‐Shakked et al.	32
5	A high and equal prevalence of the Q703K variant in NLRP3 patients with autoinflammatory symptoms and ethnically matched controls.	PubMed	Merav Lidar, Yael Shinar et al.	5
6	Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin	European Journal of Paediatric Neurology	Gali Heimer, Eran Eyal et al.	37
7	Very Early In-Utero Diagnosis of Walker-Warburg Phenotype: The Cutting Edge of Technology	SHILAP Revista de lepidopterología	R. Achiron, Eldad Katorza et al.	7
8	TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability	European Journal of Paediatric Neurology	Gali Heimer, Danit Oz-Levi et al.	27
9	Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia	Human Genetics	Ifat Bar-Joseph, Elon Pras et al.	18
10	Screening of human pluripotent stem cells using CGH and FISH reveals low-grade mosaic aneuploidy and a recurrent amplification of chromosome 1q	European Journal of Human Genetics	Ayala Aviram‐Goldring, Talia Litmanovitch et al.	29
11	Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis	The American Journal of Human Genetics	Danit Oz-Levi, Bruria Ben‐Zeev et al.	106
12	Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean Fever	Arthritis Care & Research	Dina Marek‐Yagel, Yackov Berkun et al.	13
13	Clinical disease among patients heterozygous for familial mediterranean fever	Arthritis & Rheumatism	Dina Marek‐Yagel, Yackov Berkun et al.	152
14	Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome	The American Journal of Human Genetics	Moshe Frydman, Eran Pras et al.	95
15	A novelGJB6missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis	British Journal of Dermatology	Hagit Baris, Victoria Doviner et al.	16
16	Familial pure proximal renal tubular acidosis--a clinical and genetic study	Nephrology Dialysis Transplantation	Dganit Dinour, Haike Reznik‐Wolf et al.	29
17	An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis	Journal of Investigative Dermatology	Abraham Zlotogorski, Liran Horev et al.	57
18	Somatic Mutation Analysis of theAPPandPresenilin 1and2Genes in Alzheimer's Disease Brains	Journal of Neurogenetics	Haike Reznik‐Wolf, Vahram Haroutunian et al.	5
19	Germline mutational analysis of presenilin 1 and APP genes in Jewish-Israeli individuals with familial or early-onset Alzheimer disease using denaturing gradient gel electrophoresis (DGGE)	European Journal of Human Genetics	Haike Reznik‐Wolf, Herzel Shabtai et al.	8
20	A novel mutation of presenilin 1 in familial Alzheimer's disease in Israel detected by denaturing gradient gel electrophoresis	Human Genetics	Haike Reznik‐Wolf, T. A. Treves et al.	19

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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