Philippa B. Mills

6.5k total citations
71 papers, 3.7k citations indexed

About

Philippa B. Mills is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Philippa B. Mills has authored 71 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 33 papers in Clinical Biochemistry and 11 papers in Rheumatology. Recurrent topics in Philippa B. Mills's work include Metabolism and Genetic Disorders (32 papers), Glycosylation and Glycoproteins Research (14 papers) and Biochemical and Molecular Research (12 papers). Philippa B. Mills is often cited by papers focused on Metabolism and Genetic Disorders (32 papers), Glycosylation and Glycoproteins Research (14 papers) and Biochemical and Molecular Research (12 papers). Philippa B. Mills collaborates with scholars based in United Kingdom, United States and Netherlands. Philippa B. Mills's co-authors include Peter T. Clayton, Karin Tuschl, Barbara Plecko, Matthew P. Wilson, Bryan Winchester, Cornelis Jakobs, Kevin Mills, Matthias R. Baumgartner, Eduard A. Struys and Peter M. Bramley and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Philippa B. Mills

69 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippa B. Mills United Kingdom 32 1.9k 1.1k 497 479 446 71 3.7k
Carol M. Wehr United States 20 1.8k 1.0× 380 0.3× 306 0.6× 477 1.0× 406 0.9× 25 3.6k
Carina Prip‐Buus France 34 2.1k 1.1× 640 0.6× 208 0.4× 776 1.6× 286 0.6× 64 3.4k
Rick G. Schnellmann United States 32 2.2k 1.2× 458 0.4× 164 0.3× 521 1.1× 277 0.6× 81 4.4k
Irène Ceballos-Picot France 30 1.6k 0.9× 189 0.2× 383 0.8× 388 0.8× 182 0.4× 70 3.0k
Takahito Kondo Japan 30 1.4k 0.8× 224 0.2× 268 0.5× 487 1.0× 542 1.2× 120 3.2k
Maria G. Buse United States 43 2.9k 1.6× 707 0.6× 443 0.9× 2.0k 4.2× 412 0.9× 149 6.0k
Markus Tiedge Germany 34 2.0k 1.1× 387 0.3× 302 0.6× 951 2.0× 129 0.3× 81 5.3k
Loranne Agius United Kingdom 42 2.9k 1.6× 380 0.3× 317 0.6× 1.3k 2.7× 335 0.8× 166 5.2k
Jiyang Cai United States 28 2.4k 1.3× 205 0.2× 410 0.8× 347 0.7× 551 1.2× 52 4.3k
Janine H. Santos United States 33 2.9k 1.5× 420 0.4× 177 0.4× 1.1k 2.3× 104 0.2× 59 4.3k

Countries citing papers authored by Philippa B. Mills

Since Specialization
Citations

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

Fields of papers citing papers by Philippa B. Mills

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philippa B. Mills. 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 Philippa B. Mills. The network helps show where Philippa B. Mills may publish in the future.

Co-authorship network of co-authors of Philippa B. Mills

This figure shows the co-authorship network connecting the top 25 collaborators of Philippa B. Mills. A scholar is included among the top collaborators of Philippa B. Mills 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 Philippa B. Mills. Philippa B. Mills 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.
Bandodkar, Sushil, Michael Stormon, G. A. Thomas, et al.. (2026). Liver Transplantation in PNPO Deficiency: Management Challenges and Biological Lessons. JIMD Reports. 67(1). e70067–e70067.
2.
Footitt, Emma, Michael F. Wempe, Curtis R. Coughlin, et al.. (2024). Assessment of urinary 6‐oxo‐pipecolic acid as a biomarker for ALDH7A1 deficiency. Journal of Inherited Metabolic Disease. 48(1). e12783–e12783. 5 indexed citations
3.
Thöny, Beat, Joanne Ng, Manju A. Kurian, Philippa B. Mills, & Aurora Martı́nez. (2024). Mouse models for inherited monoamine neurotransmitter disorders. Journal of Inherited Metabolic Disease. 47(3). 533–550. 2 indexed citations
4.
Sudhakar, Sniya, Amanda Lam, Philippa B. Mills, et al.. (2024). Clinical Features, Biochemistry, Imaging, and Treatment Response in a Single-Center Cohort With Coenzyme Q 10 Biosynthesis Disorders. Neurology Genetics. 10(6). e200209–e200209. 1 indexed citations
5.
Doykov, Ivan, Apostolos Papandreou, Jenny Hällqvist, et al.. (2023). New Perspectives in Dried Blood Spot Biomarkers for Lysosomal Storage Diseases. International Journal of Molecular Sciences. 24(12). 10177–10177. 6 indexed citations
6.
Wawrzynski, James, Dorothy Thompson, Dipak Ram, et al.. (2023). First in man study of intravitreal tripeptidyl peptidase 1 for CLN2 retinopathy. Eye. 38(6). 1176–1182. 4 indexed citations
7.
Mills, Philippa B., Martino L. di Salvo, Victoria I. Bunik, et al.. (2021). Characterization of Novel Pathogenic Variants Causing Pyridox(am)ine 5′-Phosphate Oxidase-Dependent Epilepsy. International Journal of Molecular Sciences. 22(21). 12013–12013. 5 indexed citations
8.
Soria, Leandro R., Sonam Gurung, Dany Perocheau, et al.. (2020). Beclin‐1‐mediated activation of autophagy improves proximal and distal urea cycle disorders. EMBO Molecular Medicine. 13(2). e13158–e13158. 16 indexed citations
9.
Iwan, Katharina, Robert Clayton, Philippa B. Mills, et al.. (2020). Urine proteomics analysis of patients with neuronal ceroid lipofuscinoses. iScience. 24(2). 102020–102020. 12 indexed citations
10.
Baruteau, Julien, Stephanie Grünewald, Marta Zancolli, et al.. (2019). Urea Cycle Related Amino Acids Measured in Dried Bloodspots Enable Long-Term In Vivo Monitoring and Therapeutic Adjustment. Metabolites. 9(11). 275–275. 3 indexed citations
11.
Reid, Emma, Apostolos Papandreou, Suzanne Drury, et al.. (2016). Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. Brain. 139(11). 2844–2854. 27 indexed citations
12.
Heywood, Wendy, Philippa B. Mills, Jale Yüzügülen, et al.. (2016). Global serum glycoform profiling for the investigation of dystroglycanopathies & Congenital Disorders of Glycosylation. Molecular Genetics and Metabolism Reports. 7. 55–62. 9 indexed citations
13.
Ibrahim, Shahnaz, et al.. (2016). Hypermanganesemia with Dystonia, Polycythemia and Cirrhosis (HMDPC) due to mutation in the SLC30A10 gene. Brain and Development. 38(9). 862–865. 32 indexed citations
14.
Darín, Niklas, Emma Reid, Laurence Prunetti, et al.. (2016). Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy. The American Journal of Human Genetics. 99(6). 1325–1337. 106 indexed citations
15.
Tuschl, Karin, Peter T. Clayton, Sídney M. Gospe, et al.. (2012). Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10 , a Manganese Transporter in Man. The American Journal of Human Genetics. 90(3). 457–466. 257 indexed citations
16.
Stamelou, María, Karin Tuschl, W.K. Chong, et al.. (2012). Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: A new treatable disorder. Movement Disorders. 27(10). 1317–1322. 87 indexed citations
17.
Salomons, Gajja S., Levinus A. Bok, Eduard A. Struys, et al.. (2007). An intriguing “silent” mutation and a founder effect in antiquitin (ALDH7A1). Annals of Neurology. 62(4). 414–418. 48 indexed citations
18.
Mills, Philippa B., Eduard A. Struys, Cornelis Jakobs, et al.. (2006). Mutations in antiquitin in individuals with pyridoxine-dependent seizures. Nature Medicine. 12(3). 307–309. 392 indexed citations
19.
Mills, Kevin, Philippa B. Mills, Marie Jackson, et al.. (2006). Diagnosis of congenital disorders of glycosylation type‐I using protein chip technology. PROTEOMICS. 6(7). 2295–2304. 25 indexed citations
20.
Mills, Philippa B., et al.. (1988). In Vivo and In Vitro 31P-NMR Preliminary Studies of the VX-2 Carcinoma in Rabbits. Investigative Radiology. 23(8). 584–891. 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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