Gabe Haller

1.0k total citations
31 papers, 548 citations indexed

About

Gabe Haller is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Gabe Haller has authored 31 papers receiving a total of 548 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Surgery. Recurrent topics in Gabe Haller's work include Connective tissue disorders research (5 papers), Nicotinic Acetylcholine Receptors Study (5 papers) and Spinal Dysraphism and Malformations (4 papers). Gabe Haller is often cited by papers focused on Connective tissue disorders research (5 papers), Nicotinic Acetylcholine Receptors Study (5 papers) and Spinal Dysraphism and Malformations (4 papers). Gabe Haller collaborates with scholars based in United States, United Kingdom and Hong Kong. Gabe Haller's co-authors include Christina A. Gurnett, Matthew B. Dobbs, David M. Alvarado, Nancy H. Miller, Brooke Sadler, Alison Goate, José A. Morcuende, Emma E. Thompson, Marcia Willing and Carole Ober and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Gabe Haller

31 papers receiving 540 citations

Peers

Gabe Haller

GENET

SURGE

CMN

PFM

Ercan Mıhçı Türkiye

Denny Schanze Germany

Michael J. Lyons United States

Thomas A. Maher United States

Leslie A. Phillips United States

Shota Takashima Japan

Alice S. Brooks Netherlands

Ondřej Souček Czechia

Pamela Knight United States

Michela Malacarne Italy

Ercan Mıhçı Türkiye

Gabe Haller

383 ×1.6

264 ×1.2

GENET

122 ×0.7

SURGE

42 ×0.5

CMN

39 ×0.6

PFM

Citations per year, relative to Gabe Haller Gabe Haller (= 1×) peers Ercan Mıhçı

Countries citing papers authored by Gabe Haller

Since Specialization

Citations

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

Fields of papers citing papers by Gabe Haller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabe Haller

This figure shows the co-authorship network connecting the top 25 collaborators of Gabe Haller. A scholar is included among the top collaborators of Gabe Haller 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 Gabe Haller. Gabe Haller 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

Haller, Gabe, et al.. (2024). Streamlined identification of clinically and functionally relevant genetic regulators of lower-tract urogenital development. Proceedings of the National Academy of Sciences. 121(6). e2309466121–e2309466121. 3 indexed citations

Yang, Peter, Peter O. Bayguinov, Carl D. Hacker, et al.. (2023). Gold nanoparticle-enhanced X-ray microtomography of the rodent reveals region-specific cerebrospinal fluid circulation in the brain. Nature Communications. 14(1). 453–453. 16 indexed citations

Tayebi, Naeimeh, Kevin McCall, Kristin Engelstad, et al.. (2023). Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome. Annals of Clinical and Translational Neurology. 10(5). 787–801. 5 indexed citations

Sadler, Brooke, Pamela A. Christopherson, Daniel B. Bellissimo, et al.. (2023). Characterization of copy-number variants in a large cohort of patients with von Willebrand disease reveals a relationship between disrupted regions and disease type. Research and Practice in Thrombosis and Haemostasis. 7(7). 102232–102232. 2 indexed citations

Li, Chengcheng, Sara K. Pittman, Jil Daw, et al.. (2023). Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E. Journal of Clinical Investigation. 133(12). 5 indexed citations

Haller, Gabe & Brooke Sadler. (2022). Elucidating the Genetic Basis of Chiari I Malformation. Neurosurgery Clinics of North America. 34(1). 55–60. 2 indexed citations

Haller, Gabe, et al.. (2022). Current and Future Approaches to Classify VUSs in LGMD-Related Genes. Genes. 13(2). 382–382. 5 indexed citations

Sadler, Brooke, Jennifer M. Strahle, Tae Sung Park, et al.. (2020). Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation. Pediatric Neurology. 106. 32–37. 33 indexed citations

Haller, Gabe, David M. Alvarado, Kevin McCall, et al.. (2016). Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine. Nature Methods. 13(11). 923–924. 11 indexed citations

10.

Haller, Gabe, David M. Alvarado, Marcia Willing, et al.. (2015). Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis. Journal of Bone and Joint Surgery. 97(17). 1411–1417. 5 indexed citations

11.

Sadler, Brooke, Gabe Haller, Howard J. Edenberg, et al.. (2015). Positive Selection on Loci Associated with Drug and Alcohol Dependence. PLoS ONE. 10(8). e0134393–e0134393. 4 indexed citations

12.

Haller, Gabe, David M. Alvarado, Kevin McCall, et al.. (2015). A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis. Human Molecular Genetics. 25(1). 202–209. 51 indexed citations

13.

Haller, Gabe, Manav Kapoor, John Budde, et al.. (2014). Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence. PMC. 1 indexed citations

14.

Buchan, Jillian G., David M. Alvarado, Gabe Haller, et al.. (2014). Are Copy Number Variants Associated With Adolescent Idiopathic Scoliosis?. Clinical Orthopaedics and Related Research. 472(10). 3216–3225. 13 indexed citations

15.

Sadler, Brooke, Gabe Haller, Arpana Agrawal, et al.. (2014). Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. Scientific Reports. 4(1). 4497–4497. 11 indexed citations

16.

Baschal, Erin E., Katherine Gowan, Nelson L.S. Tang, et al.. (2014). Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis. G3 Genes Genomes Genetics. 5(2). 167–174. 38 indexed citations

17.

Haller, Gabe, Manav Kapoor, John Budde, et al.. (2013). Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence. Human Molecular Genetics. 23(3). 810–819. 32 indexed citations

18.

Haller, Gabe, Todd E. Druley, Francesco Vallania, et al.. (2011). Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence. Human Molecular Genetics. 21(3). 647–655. 43 indexed citations

19.

Thompson, Emma E., Gabe Haller, Jayant M. Pinto, et al.. (2009). Sequence variations at the human leukocyte antigen–linked olfactory receptor cluster do not influence female preferences for male odors. Human Immunology. 71(1). 100–103. 8 indexed citations

20.

Haller, Gabe, Dara G. Torgerson, Carole Ober, & Emma E. Thompson. (2009). Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility. Journal of Allergy and Clinical Immunology. 124(6). 1204–1209.e9. 34 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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