Chris Balak

567 total citations
11 papers, 249 citations indexed

About

Chris Balak is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Chris Balak has authored 11 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Chris Balak's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA regulation and disease (2 papers). Chris Balak is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA regulation and disease (2 papers). Chris Balak collaborates with scholars based in United States, Netherlands and Hong Kong. Chris Balak's co-authors include Ashley L. Siniard, Ryan Richholt, Matthew J. Huentelman, Elizabeth Hutchins, Elizabeth Carlson, Robert R. Kitchen, Rebecca Reiman, Ashish Yeri, Joel Rozowsky and Seungchan Kim and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.

In The Last Decade

Chris Balak

10 papers receiving 247 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chris Balak United States	8	177	100	53	18	17	11	249
Ryan Richholt United States	11	218 1.2×	108 1.1×	54 1.0×	43 2.4×	44 2.6×	16	335
Anbo Zhou United States	9	167 0.9×	48 0.5×	90 1.7×	7 0.4×	21 1.2×	14	302
Kathrin Schramm Germany	7	221 1.2×	43 0.4×	56 1.1×	7 0.4×	12 0.7×	15	309
Yvan Herenger France	5	135 0.8×	51 0.5×	136 2.6×	19 1.1×	6 0.4×	6	251
Junghyun Eom South Korea	5	270 1.5×	43 0.4×	93 1.8×	11 0.6×	6 0.4×	7	336
Claudia Chavarria United States	6	215 1.2×	26 0.3×	65 1.2×	20 1.1×	9 0.5×	8	294
Carolin Walter Germany	8	181 1.0×	56 0.6×	40 0.8×	16 0.9×	20 1.2×	30	312
Sergi Villatoro Spain	11	162 0.9×	62 0.6×	185 3.5×	18 1.0×	10 0.6×	19	358
Prachi Kothiyal United States	7	171 1.0×	64 0.6×	211 4.0×	11 0.6×	9 0.5×	12	373
Taeyoung Hwang United States	10	509 2.9×	246 2.5×	35 0.7×	9 0.5×	7 0.4×	17	580

Countries citing papers authored by Chris Balak

Since Specialization

Citations

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

Fields of papers citing papers by Chris Balak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chris Balak

This figure shows the co-authorship network connecting the top 25 collaborators of Chris Balak. A scholar is included among the top collaborators of Chris Balak 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 Chris Balak. Chris Balak is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Wongkittichote, Parith, Tae‐Ik Choi, Dwight D. Koeberl, et al.. (2022). Expanding allelic and phenotypic spectrum of ZC4H2‐related disorder: A novel hypomorphic variant and high prevalence of tethered cord. Clinical Genetics. 103(2). 167–178. 5 indexed citations

Belnap, Newell, et al.. (2021). Progressive bilateral nuclear cataracts associated with cerebellar-facial-dental syndrome: case report, literature review, and identification of a new genetic variant. Journal of American Association for Pediatric Ophthalmology and Strabismus. 25(6). 370–373.

Hutchins, Elizabeth, Rebecca Reiman, Ryan Richholt, et al.. (2021). Extracellular circular RNA profiles in plasma and urine of healthy, male college athletes. Scientific Data. 8(1). 276–276. 11 indexed citations

Llaci, Lorida, Keri Ramsey, Newell Belnap, et al.. (2019). Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD). Human Genetics. 138(11-12). 1409–1417. 12 indexed citations

Das, Arup, Sampathkumar Rangasamy, Marcus Naymik, et al.. (2018). Novel Genetic Variants in Extreme Phenotypes of Diabetic Retinopathy: DRGen Study. Investigative Ophthalmology & Visual Science. 59(9). 1911–1911. 4 indexed citations

Huentelman, Matthew J., Ignazio S. Piras, Ashley L. Siniard, et al.. (2018). Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers. Frontiers in Aging Neuroscience. 10. 155–155. 22 indexed citations

Wojcik, Monica H., Kyoko Okada, Sanjay P. Prabhu, et al.. (2018). De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy. American Journal of Medical Genetics Part A. 176(12). 2623–2629. 19 indexed citations

Yeri, Ashish, Amanda Courtright, Rebecca Reiman, et al.. (2017). Total Extracellular Small RNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects. Scientific Reports. 7(1). 44061–44061. 123 indexed citations

Toro, Camilo, Roderick Hori, May Christine V. Malicdan, et al.. (2017). A recurrent de novo missense mutation in UBTF causes developmental neuroregression. Human Molecular Genetics. 27(4). 691–705. 29 indexed citations

10.

Ramsey, Keri, Newell Belnap, Szabolcs Szelinger, et al.. (2017). Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results. Seminars in Pediatric Neurology. 26. 28–32. 9 indexed citations

11.

Belnap, Newell, Ashley L. Siniard, Szabolcs Szelinger, et al.. (2016). A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia. Molecular Case Studies. 2(5). a000851–a000851. 15 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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