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 — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Haike Reznik‐Wolf Israel 15 554 171 128 118 101 39 888
Rıza Köksal Özgül Türkiye 17 457 0.8× 194 1.1× 90 0.7× 121 1.0× 72 0.7× 69 873
Oscar Suzuki United States 15 539 1.0× 109 0.6× 45 0.4× 100 0.8× 72 0.7× 25 817
Anna Maria Barbieri Italy 17 599 1.1× 336 2.0× 47 0.4× 65 0.6× 30 0.3× 37 1.1k
Shivakumar Vasanth United States 17 611 1.1× 486 2.8× 77 0.6× 83 0.7× 196 1.9× 28 1.1k
Pieter Faber United States 15 1.0k 1.9× 190 1.1× 200 1.6× 125 1.1× 31 0.3× 22 1.6k
Yves Sznajer Belgium 19 623 1.1× 373 2.2× 117 0.9× 134 1.1× 39 0.4× 50 1.1k
Satsuki Matsushima Japan 19 536 1.0× 134 0.8× 30 0.2× 279 2.4× 26 0.3× 38 1.0k
Bruno Copin France 14 452 0.8× 260 1.5× 71 0.6× 162 1.4× 376 3.7× 23 922
Louise Ocaka United Kingdom 19 729 1.3× 420 2.5× 86 0.7× 107 0.9× 357 3.5× 30 1.2k
Shuhei Nishiyama Japan 21 333 0.6× 71 0.4× 227 1.8× 23 0.2× 77 0.8× 65 1.8k

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

20 of 20 papers shown
1.
Basel‐Salmon, Lina, Noa Ruhrman‐Shahar, Ortal Barel, et al.. (2021). Biallelic variants in ETV2 in a family with congenital heart defects, vertebral abnormalities and preaxial polydactyly. European Journal of Medical Genetics. 64(2). 104124–104124. 7 indexed citations
2.
Oz, Shimrit, Hagith Yonath, Efrat Ofek, et al.. (2020). Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi Jews. International Journal of Cardiology. 317. 133–138. 11 indexed citations
3.
Pode‐Shakked, Naomi, Stanley H. Korman, Ben Pode‐Shakked, et al.. (2020). Clues and challenges in the diagnosis of intermittent maple syrup urine disease. European Journal of Medical Genetics. 63(6). 103901–103901. 13 indexed citations
4.
Greenbaum, Lior, Ben Pode‐Shakked, Haike Reznik‐Wolf, et al.. (2019). Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families. Frontiers in Genetics. 10. 425–425. 32 indexed citations
5.
Lidar, Merav, Yael Shinar, Haike Reznik‐Wolf, et al.. (2018). A high and equal prevalence of the Q703K variant in NLRP3 patients with autoinflammatory symptoms and ethnically matched controls.. PubMed. 35 Suppl 108(6). 82–85. 5 indexed citations
6.
Heimer, Gali, Eran Eyal, Xiaolin Zhu, et al.. (2017). Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin. European Journal of Paediatric Neurology. 22(1). 93–101. 37 indexed citations
7.
Achiron, R., et al.. (2016). Very Early In-Utero Diagnosis of Walker-Warburg Phenotype: The Cutting Edge of Technology. SHILAP Revista de lepidopterología. 2(2). E54–E57. 7 indexed citations
8.
Heimer, Gali, Danit Oz-Levi, Eran Eyal, et al.. (2015). TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability. European Journal of Paediatric Neurology. 20(1). 69–79. 27 indexed citations
9.
Bar-Joseph, Ifat, Elon Pras, Haike Reznik‐Wolf, et al.. (2012). Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia. Human Genetics. 131(11). 1805–1810. 18 indexed citations
10.
Aviram‐Goldring, Ayala, Talia Litmanovitch, Haike Reznik‐Wolf, et al.. (2012). 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. 20(12). 1248–1255. 29 indexed citations
11.
Oz-Levi, Danit, Bruria Ben‐Zeev, Elizabeth K. Ruzzo, et al.. (2012). Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis. The American Journal of Human Genetics. 91(6). 1065–1072. 106 indexed citations
12.
Marek‐Yagel, Dina, Yackov Berkun, Shai Padeh, et al.. (2010). Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean Fever. Arthritis Care & Research. 62(9). 1294–1298. 13 indexed citations
13.
Marek‐Yagel, Dina, Yackov Berkun, Shai Padeh, et al.. (2009). Clinical disease among patients heterozygous for familial mediterranean fever. Arthritis & Rheumatism. 60(6). 1862–1866. 152 indexed citations
14.
Frydman, Moshe, et al.. (2008). Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome. The American Journal of Human Genetics. 82(5). 1217–1222. 95 indexed citations
15.
Baris, Hagit, et al.. (2008). A novelGJB6missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis. British Journal of Dermatology. 159(6). 1373–1376. 16 indexed citations
16.
Dinour, Dganit, et al.. (2007). Familial pure proximal renal tubular acidosis--a clinical and genetic study. Nephrology Dialysis Transplantation. 23(4). 1211–1215. 29 indexed citations
17.
Zlotogorski, Abraham, Liran Horev, Dan Ben‐Amitai, et al.. (2006). An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis. Journal of Investigative Dermatology. 126(6). 1292–1296. 57 indexed citations
18.
Reznik‐Wolf, Haike, Vahram Haroutunian, Gerhard Walter, et al.. (1998). Somatic Mutation Analysis of theAPPandPresenilin 1and2Genes in Alzheimer's Disease Brains. Journal of Neurogenetics. 12(1). 55–65. 5 indexed citations
19.
Reznik‐Wolf, Haike, Herzel Shabtai, Judith Aharon‐Peretz, et al.. (1998). 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. 6(2). 176–180. 8 indexed citations
20.
Reznik‐Wolf, Haike, T. A. Treves, Michael Davidson, et al.. (1996). A novel mutation of presenilin 1 in familial Alzheimer's disease in Israel detected by denaturing gradient gel electrophoresis. Human Genetics. 98(6). 700–702. 19 indexed citations

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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