Daniel Helbling

2.3k total citations
21 papers, 689 citations indexed

About

Daniel Helbling is a scholar working on Molecular Biology, Clinical Biochemistry and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Daniel Helbling has authored 21 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Daniel Helbling's work include Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (8 papers) and Neonatal Respiratory Health Research (4 papers). Daniel Helbling is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (8 papers) and Neonatal Respiratory Health Research (4 papers). Daniel Helbling collaborates with scholars based in United States, United Kingdom and Israel. Daniel Helbling's co-authors include David Dimmock, Lital N. Adler, Ayelet Erez, Shiran Rabinovich, Alon Silberman, Sandesh C.S. Nagamani, Igor Ulitsky, Venkatesh Sampath, Noa Stettner and Alexander Brandis and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Daniel Helbling

21 papers receiving 679 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Helbling United States 12 417 189 105 78 75 21 689
Martin R. Buta United States 6 701 1.7× 269 1.4× 99 0.9× 107 1.4× 14 0.2× 18 920
Subhasree Basu United States 14 782 1.9× 445 2.4× 330 3.1× 41 0.5× 13 0.2× 22 1.1k
Scott R. Manson United States 14 379 0.9× 47 0.2× 49 0.5× 26 0.3× 14 0.2× 24 623
Magdalene K. Sgagias United States 11 361 0.9× 93 0.5× 44 0.4× 11 0.1× 36 0.5× 14 760
Alex J. Bott United States 9 438 1.1× 289 1.5× 50 0.5× 15 0.2× 8 0.1× 12 670
Guanghua Chen China 11 573 1.4× 165 0.9× 54 0.5× 6 0.1× 30 0.4× 23 1.0k
Kimie Kondo United States 15 484 1.2× 127 0.7× 65 0.6× 10 0.1× 149 2.0× 22 793
William D. Merritt United States 12 459 1.1× 41 0.2× 52 0.5× 46 0.6× 395 5.3× 19 929
Eli Moallem Israel 12 461 1.1× 62 0.3× 22 0.2× 6 0.1× 31 0.4× 13 768

Countries citing papers authored by Daniel Helbling

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Helbling

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Helbling. 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 Daniel Helbling. The network helps show where Daniel Helbling may publish in the future.

Co-authorship network of co-authors of Daniel Helbling

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Helbling. A scholar is included among the top collaborators of Daniel Helbling 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 Daniel Helbling. Daniel Helbling 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.
Batalov, Serge, Jerica Lenberg, Daniel Helbling, et al.. (2025). Long-Read Genome Sequencing in Clinical Psychiatry: RFX3 Haploinsufficiency in a Hospitalized Adolescent With Autism, Intellectual Disability, and Behavioral Decompensation. American Journal of Psychiatry. 182(8). 722–727. 1 indexed citations
2.
Helbling, Daniel, Jerica Lenberg, Arivudainambi Ramalingam, & Kristen Wigby. (2023). P483: Genome sequence re-analysis reveals de-novo FBXW7 canonical splice variant in newly described neurodevelopmental syndrome. SHILAP Revista de lepidopterología. 1(1). 100530–100530. 1 indexed citations
3.
Meng, Hui, Margaret Beatka, Daniel Helbling, et al.. (2020). The nucleotide prodrug CERC‐913 improves mtDNA content in primary hepatocytes from DGUOK‐deficient rats. Journal of Inherited Metabolic Disease. 44(2). 492–501. 6 indexed citations
4.
Rabinovich, Shiran, Alon Silberman, Lital N. Adler, et al.. (2019). The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesis. Oncogene. 39(1). 164–175. 25 indexed citations
5.
Helbling, Daniel, Julie McCarrier, Matthew Harmelink, et al.. (2019). Severe Neonatal RYR1 Myopathy With Pathological Features of Congenital Muscular Dystrophy. Journal of Neuropathology & Experimental Neurology. 78(3). 283–287. 4 indexed citations
6.
Ferdinandusse, Sacha, Joy D. Cogan, D.N. Cooper, et al.. (2018). Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant. American Journal of Medical Genetics Part A. 176(3). 692–698. 23 indexed citations
7.
Marquez, Maribel, Chris McDermott‐Roe, Daniel Helbling, et al.. (2018). Abstract 378: Evaluation of Patient Specific MTERF4 Variants in Gene Edited Human iPSC-derived Cardiomyocytes. Circulation Research. 123(Suppl_1). 1 indexed citations
8.
McDermott‐Roe, Chris, Michael Grzybowski, Maribel Marquez, et al.. (2017). Efficient Precision Genome Editing in iPSCs via Genetic Co-targeting with Selection. Stem Cell Reports. 8(3). 491–499. 25 indexed citations
9.
Scalais, Emmanuel, Linda De Meırleır, Geert A. Martens, et al.. (2017). X-Linked Cobalamin Disorder ( HCFC1 ) Mimicking Nonketotic Hyperglycinemia With Increased Both Cerebrospinal Fluid Glycine and Methylmalonic Acid. Pediatric Neurology. 71. 65–69. 10 indexed citations
10.
11.
Geddes, Gabrielle C., David Dimmock, David A. Hehir, et al.. (2015). A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia. Journal of Perinatology. 35(2). 155–157. 2 indexed citations
12.
Rabinovich, Shiran, Lital N. Adler, Keren Yizhak, et al.. (2015). Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis. Nature. 527(7578). 379–383. 264 indexed citations
13.
Mele, Caterina, Mathieu Lemaire, Paraskevas Iatropoulos, et al.. (2015). Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome. Clinical Journal of the American Society of Nephrology. 10(6). 1011–1019. 37 indexed citations
14.
Sampath, Venkatesh, Heather Menden, Daniel Helbling, et al.. (2015). SIGIRR Genetic Variants in Premature Infants With Necrotizing Enterocolitis. PEDIATRICS. 135(6). e1530–e1534. 67 indexed citations
15.
Sampath, Venkatesh, Daniel Helbling, Heather Menden, et al.. (2015). Necrotizing Enterocolitis Is Not Associated With Sequence Variants in Antioxidant Response Genes in Premature Infants. Journal of Pediatric Gastroenterology and Nutrition. 62(3). 420–423. 3 indexed citations
16.
Sampath, Venkatesh, Jeffery S. Garland, Daniel Helbling, et al.. (2014). Antioxidant response genes sequence variants and BPD susceptibility in VLBW infants. Pediatric Research. 77(3). 477–483. 46 indexed citations
17.
Helbling, Daniel, et al.. (2013). Reduced Mitochondrial DNA Content and Heterozygous Nuclear Gene Mutations in Patients With Acute Liver Failure. Journal of Pediatric Gastroenterology and Nutrition. 57(4). 438–443. 16 indexed citations
18.
Helbling, Daniel, et al.. (2012). Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathy. Molecular Genetics and Metabolism. 107(1-2). 92–94. 21 indexed citations
19.
Helbling, Daniel, et al.. (2011). Next‐generation Sequencing Facilitates the Diagnosis in a Child With Twinkle Mutations Causing Cholestatic Liver Failure. Journal of Pediatric Gastroenterology and Nutrition. 54(2). 291–294. 34 indexed citations
20.

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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