Andrew H. Crosby

13.6k total citations · 3 hit papers
125 papers, 7.1k citations indexed

About

Andrew H. Crosby is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Andrew H. Crosby has authored 125 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 36 papers in Cellular and Molecular Neuroscience and 27 papers in Neurology. Recurrent topics in Andrew H. Crosby's work include Hereditary Neurological Disorders (33 papers), Neurological diseases and metabolism (26 papers) and RNA modifications and cancer (13 papers). Andrew H. Crosby is often cited by papers focused on Hereditary Neurological Disorders (33 papers), Neurological diseases and metabolism (26 papers) and RNA modifications and cancer (13 papers). Andrew H. Crosby collaborates with scholars based in United Kingdom, United States and Pakistan. Andrew H. Crosby's co-authors include Christos Proukakis, Michael A. Patton, Steve Jeffery, Thomas T. Warner, Kamini Kalidas, Michael A. Simpson, Bruce D. Gelb, Marco Tartaglia, Han G. Brunner and Raju Kucherlapati and has published in prestigious journals such as The Lancet, Circulation and Nature Genetics.

In The Last Decade

Andrew H. Crosby

120 papers receiving 7.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

2001 1.2k citations Marco Tartaglia, Han G. Brunner et al. Nature Genetics profile →
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)

2000 747 citations Andrew H. Crosby, Steve Jeffery et al. profile →
PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

2002 522 citations Marco Tartaglia, Kamini Kalidas et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew H. Crosby United Kingdom	36	3.9k	1.7k	1.3k	1.0k	1.0k	125	7.1k
John S. Rudge United States	38	6.4k 1.6×	1.7k 1.0×	1.0k 0.8×	534 0.5×	630 0.6×	57	10.9k
Christiana Ruhrberg United Kingdom	49	6.8k 1.7×	3.0k 1.8×	1.2k 0.9×	813 0.8×	2.1k 2.1×	113	11.2k
Guillem Genové Sweden	27	3.4k 0.9×	689 0.4×	712 0.6×	2.4k 2.3×	661 0.6×	42	7.5k
Joyce McClain United States	15	5.2k 1.4×	2.0k 1.2×	843 0.7×	312 0.3×	586 0.6×	17	8.3k
Annika Armulik Sweden	19	3.9k 1.0×	871 0.5×	788 0.6×	2.7k 2.6×	919 0.9×	20	8.7k
Chitra Suri United States	15	6.4k 1.7×	1.3k 0.8×	685 0.5×	327 0.3×	697 0.7×	19	9.2k
Joseph M. Miano United States	54	7.5k 1.9×	539 0.3×	1.2k 0.9×	278 0.3×	871 0.9×	134	10.7k
Thomas H. Aldrich United States	15	5.7k 1.5×	2.1k 1.3×	1.1k 0.8×	262 0.3×	768 0.8×	17	8.7k
Haluk Topaloğlu Türkiye	49	5.5k 1.4×	1.8k 1.1×	372 0.3×	376 0.4×	1.5k 1.5×	261	8.2k
Peter C. Maisonpierre United States	21	9.6k 2.5×	3.7k 2.2×	851 0.7×	440 0.4×	1.2k 1.1×	26	14.2k

Countries citing papers authored by Andrew H. Crosby

Since Specialization

Citations

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

Fields of papers citing papers by Andrew H. Crosby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew H. Crosby. 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 Andrew H. Crosby. The network helps show where Andrew H. Crosby may publish in the future.

Co-authorship network of co-authors of Andrew H. Crosby

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew H. Crosby. A scholar is included among the top collaborators of Andrew H. Crosby 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 Andrew H. Crosby. Andrew H. Crosby 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

Fasham, James, Adam C. Gunning, Martina Owens, et al.. (2024). TECPR2‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine. American Journal of Medical Genetics Part A. 194(7). e63579–e63579. 2 indexed citations

Rawlins, Lettie E., Niamat Khan, Saadullah Khan, et al.. (2024). Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan. BMC Neurology. 24(1). 394–394. 1 indexed citations

Rawlins, Lettie E., Hannah Jones, Olivia Wenger, et al.. (2021). A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder. PLoS Genetics. 17(9). e1009803–e1009803. 6 indexed citations

Gunning, Adam C., James Fasham, Andrew H. Crosby, et al.. (2020). Assessing performance of pathogenicity predictors using clinically relevant variant datasets. Journal of Medical Genetics. 58(8). 547–555. 69 indexed citations

Wenger, Olivia, Devyani Chowdhury, Andrew H. Crosby, et al.. (2020). Biochemical phenotype and its relationship to treatment in 16 individuals with PCCB c.1606A > G (p.Asn536Asp) variant propionic acidemia. Molecular Genetics and Metabolism. 131(3). 316–324. 1 indexed citations

Fasham, James, Jamie Harrison, Katie B. Williams, et al.. (2020). No association between SCN9A and monogenic human epilepsy disorders. PLoS Genetics. 16(11). e1009161–e1009161. 11 indexed citations

Harlalka, Gaurav V., Shamshad Ali, Siying Lin, et al.. (2019). Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families. Eye. 33(8). 1339–1346. 8 indexed citations

Baple, Emma L., Ashley J. Russo, Judith Brown, et al.. (2017). An Amish founder mutation disrupts a PI(3)P-WHAMM-Arp2/3 complex–driven autophagosomal remodeling pathway. Molecular Biology of the Cell. 28(19). 2492–2507. 19 indexed citations

Alakbarzade, Vafa, Abdul Hameed, Debra Q Y Quek, et al.. (2015). A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome. Nature Genetics. 47(7). 814–817. 117 indexed citations

10.

Alswaid, Abdulrahman, et al.. (2013). Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome. American Journal of Medical Genetics Part A. 161(12). 3155–3160. 33 indexed citations

11.

Crosby, Andrew H., Heema Patel, Barry A. Chioza, et al.. (2010). Defective Mitochondrial mRNA Maturation Is Associated with Spastic Ataxia. The American Journal of Human Genetics. 87(5). 655–660. 58 indexed citations

12.

Chaleshtori, Morteza Hashemzadeh, et al.. (2008). Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases. SHILAP Revista de lepidopterología. 5 indexed citations

13.

Cross, Harold E. & Andrew H. Crosby. (2008). Amish Contributions to Medical Genetics. 82(3). 449–467. 5 indexed citations

14.

Ouahchi, Karim, Thomas T. Warner, Yi Yang, et al.. (2008). Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration. The American Journal of Human Genetics. 82(2). 510–515. 117 indexed citations

15.

Sen‐Chowdhry, Srijita, Petros Syrris, William J. McKenna, et al.. (2006). Letter regarding article by Norman et al, "Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy" - Response. UCL Discovery (University College London).

16.

Tartaglia, Marco, Kamini Kalidas, Adam Shaw, et al.. (2002). PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity. The American Journal of Human Genetics. 70(6). 1555–1563. 522 indexed citations breakdown →

17.

Simpson, Michael A., et al.. (2001). Screening of British CADASIL families for NOTCH 3 mutations. Journal of Medical Genetics. 38. 1 indexed citations

18.

Patel, Harshad B., Paul Hart, Thomas T. Warner, et al.. (2001). Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci. American Journal of Medical Genetics. 102(1). 68–72. 7 indexed citations

19.

Crosby, Andrew H., et al.. (1999). Evidence from a Ghanaian Population of Known African Descent to Support the Proposition That Hemochromatosis Is a Caucasian Disorder. Genetic Testing. 3(4). 375–377. 10 indexed citations

20.

Crosby, Andrew H., Steven Jeffery, Tessa Homfray, Rohan Taylor, & Michael A. Patton. (1999). Prenatal Diagnosis and the Subsequent Mutation Analysis in a Family with Carbohydrate-Deficient Glycoprotein Type I Syndrome: Growing Evidence to Support Founder Effects within CDG1 Populations. Genetic Testing. 3(3). 305–307. 3 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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