Natalie Hauser

1.8k total citations
26 papers, 562 citations indexed

About

Natalie Hauser is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Natalie Hauser has authored 26 papers receiving a total of 562 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Clinical Biochemistry. Recurrent topics in Natalie Hauser's work include Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Natalie Hauser is often cited by papers focused on Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Natalie Hauser collaborates with scholars based in United States, Australia and Canada. Natalie Hauser's co-authors include Charles P. Venditti, Irini Manoli, Jennifer L. Sloan, Dale L. Bodian, Thierry Vilboux, Helen H. Hobbs, Jonathan J. Rios, Abhimanyu Garg, André Bensadoun and Jonathan C. Cohen and has published in prestigious journals such as American Journal of Clinical Nutrition, American Journal of Neuroradiology and Pediatric Research.

In The Last Decade

Natalie Hauser

26 papers receiving 558 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natalie Hauser United States 13 293 228 111 88 74 26 562
Almundher Al‐Maawali Oman 14 312 1.1× 142 0.6× 57 0.5× 65 0.7× 80 1.1× 55 605
Pilar Magoulas United States 15 383 1.3× 290 1.3× 147 1.3× 57 0.6× 27 0.4× 24 727
Gözde Yeşil Türkiye 15 290 1.0× 205 0.9× 30 0.3× 32 0.4× 45 0.6× 78 679
Rehab Ali Qatar 14 286 1.0× 212 0.9× 62 0.6× 35 0.4× 37 0.5× 21 554
Tawfeg Ben‐Omran Qatar 11 353 1.2× 225 1.0× 61 0.5× 17 0.2× 41 0.6× 24 584
Tomàs Pinós Spain 17 347 1.2× 232 1.0× 67 0.6× 22 0.3× 89 1.2× 58 810
Geetha Anand United Kingdom 13 303 1.0× 105 0.5× 77 0.7× 22 0.3× 39 0.5× 34 565
Khalid Al‐Thihli Oman 13 219 0.7× 116 0.5× 135 1.2× 29 0.3× 27 0.4× 50 456
Ardinger Hh United States 6 192 0.7× 124 0.5× 56 0.5× 28 0.3× 27 0.4× 287 402
Adam Mp 6 180 0.6× 113 0.5× 56 0.5× 28 0.3× 25 0.3× 286 388

Countries citing papers authored by Natalie Hauser

Since Specialization
Citations

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

Fields of papers citing papers by Natalie Hauser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalie Hauser

This figure shows the co-authorship network connecting the top 25 collaborators of Natalie Hauser. A scholar is included among the top collaborators of Natalie Hauser 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 Natalie Hauser. Natalie Hauser 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.
Hauser, Natalie, Sumit Punj, Katrina Prescott, et al.. (2020). Mosaicism in ASXL3-related syndrome: Description of five patients from three families. European Journal of Medical Genetics. 63(6). 103925–103925. 9 indexed citations
2.
Kane, Megan, et al.. (2019). Endosomal trafficking defects in patient cells with KIAA1109 biallelic variants. Genes & Diseases. 6(1). 56–67. 17 indexed citations
3.
Bodian, Dale L., Thierry Vilboux, & Natalie Hauser. (2019). Genotype-first analysis of a generally healthy population cohort supports genetic testing for diagnosis of hereditary angioedema of unknown cause. Allergy Asthma and Clinical Immunology. 15(1). 32–32. 8 indexed citations
4.
Hauser, Natalie, et al.. (2019). A case study of atypical Larsen syndrome with absent hallmark joint dislocations. Molecular Genetics & Genomic Medicine. 7(5). e648–e648. 1 indexed citations
5.
Bodian, Dale L., Prachi Kothiyal, & Natalie Hauser. (2018). Pitfalls of clinical exome and gene panel testing: alternative transcripts. Genetics in Medicine. 21(5). 1240–1245. 11 indexed citations
6.
Larson, Austin, Shanti Balasubramaniam, John Christodoulou, et al.. (2018). Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6. Mitochondrion. 44. 58–64. 17 indexed citations
7.
Bodian, Dale L., John M. Schreiber, Thierry Vilboux, Alina Khromykh, & Natalie Hauser. (2018). Mutation in an alternative transcript ofCDKL5in a boy with early-onset seizures. Molecular Case Studies. 4(3). a002360–a002360. 9 indexed citations
8.
Bodian, Dale L., Thierry Vilboux, Suchitra K. Hourigan, et al.. (2017). Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy. Molecular Case Studies. 3(6). a002055–a002055. 12 indexed citations
9.
Bodian, Dale L., Thierry Vilboux, Alina Khromykh, et al.. (2017). Utilization of genomic sequencing for population screening of immunodeficiencies in the newborn. Genetics in Medicine. 19(12). 1367–1375. 22 indexed citations
10.
Cusmano‐Ozog, Kristina, et al.. (2016). Diagnosis of LCHAD/TFP deficiency in an at risk newborn using umbilical cord blood acylcarnitine analysis. Molecular Genetics and Metabolism Reports. 10. 8–10. 3 indexed citations
11.
Paul, Scott M., Natalie Hauser, Jennifer L. Sloan, et al.. (2015). Delineating the spectrum of impairments, disabilities, and rehabilitation needs in methylmalonic acidemia (MMA). American Journal of Medical Genetics Part A. 167(9). 2075–2084. 15 indexed citations
12.
Shang, Linshan, Lindsay B. Henderson, Megan T. Cho, et al.. (2015). De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism. Neurogenetics. 17(1). 43–49. 52 indexed citations
13.
Strickland, Alleene V., Maria Schabhüttl, H. Offenbacher, et al.. (2015). Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1. Journal of Neurology. 262(9). 2124–2134. 49 indexed citations
14.
Al‐Kateb, Hussam, Geetika Khanna, Isabel Filges, et al.. (2014). Scoliosis and vertebral anomalies: Additional abnormal phenotypes associated with chromosome 16p11.2 rearrangement. American Journal of Medical Genetics Part A. 164(5). 1118–1126. 29 indexed citations
15.
Weh, Eric, Linda M. Reis, Hannah C. Happ, et al.. (2014). Whole exome sequence analysis of Peters anomaly. Human Genetics. 133(12). 1497–1511. 53 indexed citations
16.
Baker, Eva H., Jennifer L. Sloan, Natalie Hauser, et al.. (2014). MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia. American Journal of Neuroradiology. 36(1). 194–201. 33 indexed citations
17.
Prust, Morgan J., Andrea Gropman, & Natalie Hauser. (2011). New frontiers in neuroimaging applications to inborn errors of metabolism. Molecular Genetics and Metabolism. 104(3). 195–205. 6 indexed citations
18.
Hauser, Natalie, Irini Manoli, Jennifer Graf, Jennifer L. Sloan, & Charles P. Venditti. (2010). Variable dietary management of methylmalonic acidemia: metabolic and energetic correlations. American Journal of Clinical Nutrition. 93(1). 47–56. 43 indexed citations
19.
Koral, Korgün, et al.. (2009). Hyperlipidemia Resulting in Abnormal Density and Signal Intensity of Blood in a Neonate with Lipoprotein Lipase Deficiency: Fig 1.. American Journal of Neuroradiology. 31(10). 1999–2000. 2 indexed citations
20.
Crider, Bill P., et al.. (2008). Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease. Pediatric Research. 64(4). 358–363. 74 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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