Phil Ancliff

1.7k total citations
25 papers, 871 citations indexed

About

Phil Ancliff is a scholar working on Genetics, Hematology and Immunology. According to data from OpenAlex, Phil Ancliff has authored 25 papers receiving a total of 871 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 10 papers in Hematology and 10 papers in Immunology. Recurrent topics in Phil Ancliff's work include Blood disorders and treatments (16 papers), Immunodeficiency and Autoimmune Disorders (10 papers) and Erythrocyte Function and Pathophysiology (7 papers). Phil Ancliff is often cited by papers focused on Blood disorders and treatments (16 papers), Immunodeficiency and Autoimmune Disorders (10 papers) and Erythrocyte Function and Pathophysiology (7 papers). Phil Ancliff collaborates with scholars based in United Kingdom, United States and India. Phil Ancliff's co-authors include David C. Linch, Rosemary E. Gale, Ian Hann, Ri Liesner, Adrian J. Thrasher, Christine Kinnon, Michael P. Blundell, Yolanda Calle, Helena Kempski and Gareth E. Jones and has published in prestigious journals such as The Journal of Experimental Medicine, The Journal of Cell Biology and Blood.

In The Last Decade

Phil Ancliff

24 papers receiving 858 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Phil Ancliff United Kingdom 15 400 349 230 225 166 25 871
Brigitte Kasper Germany 15 183 0.5× 574 1.6× 412 1.8× 173 0.8× 74 0.4× 22 1.0k
Erin Janssen United States 17 188 0.5× 952 2.7× 340 1.5× 339 1.5× 105 0.6× 34 1.4k
Elizabeth Garabedian United States 16 258 0.6× 506 1.4× 85 0.4× 179 0.8× 46 0.3× 35 843
Nancy Pech United States 15 278 0.7× 398 1.1× 143 0.6× 299 1.3× 91 0.5× 26 764
Wolfgang Schuh Germany 20 107 0.3× 677 1.9× 193 0.8× 423 1.9× 52 0.3× 45 1.2k
Claude Capron France 15 67 0.2× 164 0.5× 301 1.3× 299 1.3× 54 0.3× 32 768
Maria Carmina Castiello Italy 17 305 0.8× 345 1.0× 74 0.3× 320 1.4× 18 0.1× 27 785
Rami Khoriaty United States 16 107 0.3× 101 0.3× 213 0.9× 290 1.3× 184 1.1× 53 766
Maurilia Fiorini Italy 18 290 0.7× 640 1.8× 229 1.0× 264 1.2× 20 0.1× 27 1.3k
Takao Yoshihara Japan 17 129 0.3× 217 0.6× 347 1.5× 306 1.4× 37 0.2× 62 885

Countries citing papers authored by Phil Ancliff

Since Specialization
Citations

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

Fields of papers citing papers by Phil Ancliff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Phil Ancliff

This figure shows the co-authorship network connecting the top 25 collaborators of Phil Ancliff. A scholar is included among the top collaborators of Phil Ancliff 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 Phil Ancliff. Phil Ancliff 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.
Connor, Philip, Michelle Cummins, Michael Gattens, et al.. (2024). Blinatumomab with De-Escalated Chemotherapy for Infant KMT2A-Rearranged B-Cell Acute Lymphoblastic Leukemia. Blood. 144(Supplement 1). 2816–2816. 3 indexed citations
2.
Donadieu, Jean, Flore Sicre de Fontbrune, Gioacchino Andrea Rotulo, et al.. (2021). Chronic neutropenia: how best to assess severity and approach management?. Expert Review of Hematology. 14(10). 945–960. 6 indexed citations
3.
Germeshausen, Manuela, Phil Ancliff, Jaime Estrada, et al.. (2018). MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia. Blood Advances. 2(6). 586–596. 69 indexed citations
4.
5.
Pearce, Kerra, Tony Brooks, Michael Hubank, et al.. (2017). Targeting acute myeloid leukemia by drug-induced c-MYB degradation. Leukemia. 32(4). 882–889. 78 indexed citations
6.
Pichler, Judith, Rosan Meyer, Jutta Köglmeier, Phil Ancliff, & Neil Shah. (2015). Nutritional Status in Children With Shwachman-Diamond Syndrome. Pancreas. 44(4). 590–595. 8 indexed citations
7.
Green, Claire L., Kiran Tawana, Robert K. Hills, et al.. (2013). GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations. British Journal of Haematology. 161(5). 701–705. 38 indexed citations
8.
Shah, Neil, Jutta Köglmeier, C Mason, et al.. (2010). Enteropathic histopathological features may be associated with Shwachman–Diamond syndrome: Figure 1. Journal of Clinical Pathology. 63(7). 592–594. 16 indexed citations
9.
Bouma, Gerben, Phil Ancliff, Adrian J. Thrasher, & Siobhan O. Burns. (2010). Recent advances in the understanding of genetic defects of neutrophil number and function. British Journal of Haematology. 151(4). 312–326. 39 indexed citations
10.
Ancliff, Phil, et al.. (2009). Type II Gaucher disease manifesting as haemophagocytic lymphohistiocytosis. Journal of Inherited Metabolic Disease. 32(S1). 107–110. 17 indexed citations
11.
Connor, Philip, Kate Khair, Ri Liesner, et al.. (2008). Stem cell transplantation for children with Glanzmann thrombasthenia. British Journal of Haematology. 140(5). 568–571. 22 indexed citations
12.
Smith, Bradley, Phil Ancliff, Arnold Pizzey, et al.. (2008). Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds. British Journal of Haematology. 144(5). 762–770. 14 indexed citations
13.
Moulding, Dale, Michael P. Blundell, David G. Spiller, et al.. (2007). Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia. The Journal of Experimental Medicine. 204(9). 2213–2224. 123 indexed citations
14.
Smith, Bradley, Phil Ancliff, David C. Linch, & Rosemary E. Gale. (2007). Identification of Two Novel Homozygous HAX1 Mutations in an Autosomal Recessive Jewish and Two Unrelated Sporadic British Families with Severe Congenital Neutropenia.. Blood. 110(11). 3309–3309. 2 indexed citations
15.
Ancliff, Phil, Michael P. Blundell, Giles O. Cory, et al.. (2006). Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia. Blood. 108(7). 2182–2189. 156 indexed citations
16.
Pai, Irumee, et al.. (2005). Ectopic thymus presenting as a subglottic mass: diagnostic and management dilemmas. International Journal of Pediatric Otorhinolaryngology. 69(4). 573–576. 14 indexed citations
17.
Fuente, Josu de la, Sue Richards, David Webb, et al.. (2005). Acute Lymphoblastic Leukaemia Has a Poor Outcome in Children with Down Syndrome Due to Infective Death in Remission (Results of UK MRC ALL 97 Trial).. Blood. 106(11). 873–873. 3 indexed citations
18.
Ancliff, Phil, Rosemary E. Gale, Ri Liesner, Ian Hann, & David C. Linch. (2003). Long‐term follow‐up of granulocyte colony‐stimulating factor receptor mutations in patients with severe congenital neutropenia: implications for leukaemogenesis and therapy. British Journal of Haematology. 120(4). 685–690. 32 indexed citations
19.
Ancliff, Phil, Rosemary E. Gale, & David C. Linch. (2003). Neutrophil Elastase Mutations in Congenital Neutropenia. Hematology. 8(3). 165–171. 13 indexed citations
20.
Ancliff, Phil, Rosemary E. Gale, Michael Watts, et al.. (2002). Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia. Blood. 100(2). 707–709. 57 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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