Anne Philippi

2.8k citations

33 papers · 1.9k indexed · h-index 20

Co-authors: Olivier Lichtarge Philippe Froguel Florence Démenais Srinivasan Madabushi Jörg Hager Gilberto Velho Nathalie Vionnet Mathew E. Sowa
Topics: Genetics and Neurodevelopmental Disorders (6 papers)Pancreatic function and diabetes (6 papers)Metabolism, Diabetes, and Cancer (6 papers)
Cited by: Genetics Endocrine and Autonomic Systems Molecular Biology
Journals: Journal of Biological Chemistry Journal of Clinical Investigation Nature Genetics
Partner nations: France United States United Kingdom

In The Last Decade

Anne Philippi

33 papers receiving 1.9k citations

Peers

Countries citing papers authored by Anne Philippi

Since Specialization

Citations

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

Fields of papers citing papers by Anne Philippi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Philippi

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

#	Work	Indexed citations
1	dUTPase (DUT) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure 2017 ·Diabetes ·Reinaldo S. Dos Santos,(unknown),Anne Philippi,(unknown),Lorella Marselli,(unknown),Valérie Senée,Delphine Bacq,Céline Besse,Baz Baz,Laura Marroquí,S. S. Ivanoff,Julien Masliah-Planchon,Marc Nicolino,Jean Soulier,(unknown),Décio L. Eizirik,Jean–François Gautier,Cécile Julier	19
2	HeterozygousHTRA1mutations are associated with autosomal dominant cerebral small vessel disease 2015 ·Brain ·Edgard Verdura,Dominique Hervé,Eva Scharrer,Maria del Mar Amador,Lucie Guyant‐Maréchal,Anne Philippi,Astrid Corlobé,Françoise Bergametti,Steven Gazal,(unknown),Nathalie Beaufort,(unknown),(unknown),Martin Dichgans,Hugues Chabriat,Christof Haffner,Elisabeth Tournier‐Lasserve	123
3	Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism 2008 ·Human Molecular Genetics ·Gilles Maussion,Jérôme Carayol,Aude-Marie Lepagnol-Bestel,Frédéric Torès,Yann Loe-Mie,Ulla Milbreta,F. Rousseau,Karine Fontaine,(unknown),Jean‐Marie Moalic,Anne Philippi,Alain Chédotal,Philip Gorwood,Nicolás Ramoz,Jörg Hager,Michel Simonneau	58
4	Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis 2007 ·BMC Medical Genetics ·Anne Philippi,Frédéric Torès,Jérôme Carayol,Francis Rousseau,Mélanie Letexier,(unknown),Pierre Lindenbaum,(unknown),Karine Fontaine,(unknown),(unknown),Peter Brooks,Jörg Hager	30
5	Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment 2006 ·Genetic Epidemiology ·Jérôme Carayol,Anne Philippi,Frédéric Torès	3
6	Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism 2005 ·Molecular Psychiatry ·Anne Philippi,(unknown),Frédéric Torès,Pierre Lindenbaum,(unknown),(unknown),Charles Marcaillou,Karine Fontaine,(unknown),Sudipta Roy,Stéphane Maillard,(unknown),Jean‐Paul Saraiva,Peter Brooks,F. Rousseau,Jörg Hager	53
7	Evolution of neural precursor selection: functional divergence of proneural proteins 2004 ·Development ·Xiao‐Jiang Quan,Tinneke Denayer,Jiekun Yan,Hamed Jafar‐Nejad,Anne Philippi,Olivier Lichtarge,Kris Vleminckx,Bassem A. Hassan	50
8	Evolutionary Trace of G Protein-coupled Receptors Reveals Clusters of Residues That Determine Global and Class-specific Functions 2004 ·Journal of Biological Chemistry ·Srinivasan Madabushi,Alecia K. Gross,Anne Philippi,Elaine C. Meng,Theodore G. Wensel,Olivier Lichtarge	167
9	Evolutionary Traces of Functional Surfaces along G Protein Signaling Pathway 2002 ·Methods in enzymology on CD-ROM/Methods in enzymology ·Olivier Lichtarge,Mathew E. Sowa,Anne Philippi	28
10	Structural clusters of evolutionary trace residues are statistically significant and common in proteins 2002 ·Journal of Molecular Biology ·Srinivasan Madabushi,Hui Yao,M. S. Marsh,David M. Kristensen,Anne Philippi,Mathew E. Sowa,Olivier Lichtarge	154
11	Lysine 270 in the Third Intracellular Domain of the Oxytocin Receptor is an Important Determinant for Gα_qCoupling Specificity 2002 ·Molecular Endocrinology ·Ming Yang,Wei Wang,Miao Zhong,Anne Philippi,Olivier Lichtarge,Barbara M. Sanborn	18
12	Indication of linkage of serum IgE levels to the interleukin-4 gene and exclusion of the contribution of the (-590 C to T) interleukin-4 promoter polymorphism to IgE variation 1999 ·Genetic Epidemiology ·Marie‐Hélène Dizier,Andrew J. Sandford,Andrew J. Walley,Anne Philippi,William Cookson,Florence Démenais	34
13	Genetic model‐free linkage analysis using the maximum‐likelihood‐binomial method for categorical traits 1999 ·Genetic Epidemiology ·Alexandre Alcaïs,Anne Philippi,Laurent Abel	10
14	CoPE: a collaborative pedigree drawing environment. 1999 ·Bioinformatics ·(unknown),Sophie Gallina,Anne Philippi,Florence Démenais,Guy Vaysseix,Emmanuel Barillot	16
15	A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus. 1998 ·Journal of Clinical Investigation ·El Habib Hani,Laurence Suaud,Philippe Boutin,Jean-Claude Chèvre,Éric Durand,Anne Philippi,Florence Démenais,Nathalie Vionnet,Hiroto Furuta,Gilberto Velho,Graeme I. Bell,Bernard Laine,Philippe Froguel	95
16	Affected sib-pair tests for linkage: Type I errors with dependent sib-pairs 1997 ·Genetic Epidemiology ·(unknown),Anne Philippi,María Martínez,Florence Démenais	14
17	Candidate gene approach of familial morbid obesity: linkage analysis of the glucocorticoid receptor gene. 1996 ·PubMed ·Karine Clément,Anne Philippi,(unknown),(unknown),Jörg Hager,Florence Démenais,A Basdevant,B Guy-Grand,Philippe Froguel	45
18	Indication for genetic linkage of the phosphoenolpyruvate carboxykinase (PCK1) gene region on chromosome 20q to non-insulin-dependent diabetes mellitus. 1996 ·PubMed ·(unknown),Habib Zouali,Anne Philippi,(unknown),Nathalie Vionnet,P Passa,Florence Démenais,Philippe Froguel	18
19	A missense mutation in the glucagon receptor gene is associated with non–insulin–dependent diabetes mellitus 1995 ·Nature Genetics ·(unknown),Lone Hansen,Christian Vaisse,Nathalie Vionnet,Anne Philippi,Wolfgang Poller,Gilberto Velho,Carlo Carcassi,Laura Contu,Cécile Julier,(unknown),P Passa,Mark Lathrop,Wayne Kindsvogel,Florence Démenais,Erica Nishimura,Philippe Froguel	126
20	A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q 1995 ·Nature Genetics ·Martine Vaxillaire,Valérie Boccio,Anne Philippi,Corinne Vigouroux,(unknown),P Passa,J. Beckmann,Gilberto Velho,G.M. Lathrop,Philippe Froguel	141

About Anne Philippi

Anne Philippi is a scholar working on Genetics, Molecular Biology and Neurology, having authored 33 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Pancreatic function and diabetes (6 papers) and Metabolism, Diabetes, and Cancer (6 papers). The work is most often cited by research in Genetics (807 citations), Endocrine and Autonomic Systems (190 citations) and Molecular Biology (1000 citations). Anne Philippi has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Olivier Lichtarge, Philippe Froguel, Florence Démenais, Srinivasan Madabushi, Jörg Hager, Gilberto Velho, Nathalie Vionnet, Mathew E. Sowa, Alecia K. Gross and Elaine C. Meng. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

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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