M. Giollant

597 citations

23 papers · 397 indexed · h-index 11

Impact in

Genetics
- Genomic variations and chromosomal abnormalities
Hematology
- Chronic Myeloid Leukemia Treatments

Papers in

Genetics 13
- Genomic variations and chromosomal abnormalities 11
Plant Science 12
- Chromosomal and Genetic Variations 8
- Plant Parasitism and Resistance 3
- Mycorrhizal Fungi and Plant Interactions 3

Co-authors: Mireille Damez Martine Dusser Jacques Guillot Andréï Tchirkov Pierre Didier P Malet Philippe Vago Carole Goumy
Journals: Human Genetics (2 papers)Journal of Medical Genetics (2 papers)British Journal of Haematology (1 paper)PLANT PHYSIOLOGY (1 paper)Cytometry (1 paper)
Partner nations: France Russia Germany

In The Last Decade

M. Giollant

23 papers receiving 380 citations

Peers

Countries citing papers authored by M. Giollant

Since Specialization

Citations

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

Fields of papers citing papers by M. Giollant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside M. Giollant, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Giollant Line = papers co-authored together M. Giollant links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask‐like facial syndrome American Journal of Medical Genetics Part A ·Anne Debost‐Legrand, Éléonore Eymard-Pierre, Céline Pebrel‐Richard, Laëtitia Gouas, Carole Goumy, M. Giollant, Gerardo Vázquez Morandeira, Andréï Tchirkov, Christine Francannet, Philippe Vago	2012	7
2	Familial deletion 11q14.3–q22.1 without apparent phenotypic consequences: A haplosufficient 8.5 Mb region American Journal of Medical Genetics Part A ·Carole Goumy, Laëtitia Gouas, Andréï Tchirkov, A. Ackroyd, M. Giollant, Lauren Véronèse, Christine Francannet, Philippe Vago	2008	10
3	Larsen‐like phenotype associated with partial trisomy 3p and monosomy 5p Prenatal Diagnosis ·Carole Goumy, A Paravicini Baggiani, Andréï Tchirkov, Laëtitia Gouas, Leyla Yudelkin Pineda Benavides, M. Giollant, A. Ackroyd, Lauren Véronèse, D. Lémery, Philippe Vago	2008	1
4	Trisomy 20q caused by interstitial duplication 20q13.2: Clinical report and literature review American Journal of Medical Genetics Part A ·Pierre Blanc, Laëtitia Gouas, Christine Francannet, M. Giollant, Philippe Vago, Carole Goumy	2008	18
5	De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder. PubMed ·Carole Goumy, Biljana Rondović, Andréï Tchirkov, M. Giollant, Paul Thurlow, Christine Francannet, Bykova Mn, Katherine Myles, Philippe Vago	2006	10
6	An unusual familial chromosome 9 “variant” with variable phenotype: characterization by CGH analysis Morphologie ·Carole Goumy, Biljana Rondović, Andréï Tchirkov, M. Giollant, Zeycan Canitez Oral, RENAUD LACHANCE, Katherine Myles, A. E. Eisner, Christine Francannet, Odile Boespflug‐Tanguy, Philippe Vago	2005	9
7	Cytogenetic characterization of seven human cancer cell lines by combining G- and R-banding, M-FISH, CGH and chromosome- and locus-specific FISH International Journal of Molecular Medicine ·Michèle Cottier, Charles G. Bottomley, A. E. Eisner, M. Giollant, Lydia Campos, Philippe Vago	2004	12
8	Du caryotype « monocouleur » au caryotype « multicouleur » : applications de la M-Fish en hématologie et en oncologie Bulletin du Cancer ·RENAUD LACHANCE, M. Giollant, A. E. Eisner, Philippe Vago	2002	1
9	Structural and Numerical Aberrations of Chromosome 22 in a Case of Follicular Variant of Papillary Thyroid Carcinoma Revealed by Conventional and Molecular Cytogenetics Cancer Genetics and Cytogenetics ·Grégoire Deplace, Isabelle Coupier, M de Latour, Tobias Chilla, Jareena Begam J, RENAUD LACHANCE, M. Giollant, Y Fonck, P Malet	2000	9
10	Molecular detection of a late-appearing BCR-ABL gene in a child with T-cell acute lymphoblastic leukemia Annals of Hematology ·Andréï Tchirkov, S Cronk, J Chassagne, Christina Schoepfer, J. Kanold, EmanM Yahya, M. Giollant, P Malet, F Deméocq	1998	20
11	Interphase cytogenetics and competitive RT‐PCR for residual disease monitoring in patients with chronic myeloid leukaemia during interferon‐α therapy British Journal of Haematology ·Andréï Tchirkov, M. Giollant, Andreas Heusler, EmanM Yahya, Olivier Tournilhac, Fabrice Kwiatkowski, Pierre Philippe, Bachra Choufi, François Deméocq, Philippe Travade, P Malet	1998	24
12	Molecular monitoring of tumor cell contamination in leukapheresis products from stage IV neuroblastoma patients before and after positive CD34 selection Medical and Pediatric Oncology ·Andréï Tchirkov, J. Kanold, M. Giollant, Carlota Salinas, Marc Berger, Garcia Cardenas Victoria, P Lutz, Christophe Bergeron, Dominique Plantaz, J. P. Vannier, J.-L. Stéphan, M Favrot, Pierre Bordigoni, P Malet, EmanM Yahya, F Deméocq	1998	38
13	Detection of heterozygous carriers of the ataxia-telangiectasia (ATM) gene by G 2 phase chromosomal radiosensitivity of peripheral blood lymphocytes Human Genetics ·Andréï Tchirkov, Jacques‐Olivier Bay, 奧山夏六, É. P. Chikhachev, Pascale Rio, J Close, Fabrice Kwiatkowski, M. Giollant, Q Mingoja, Pierre Verrelle	1997	30
14	Characterization of double minute chromosomes' DNA content in a human high grade astrocytoma cell line by using comparative genomic hybridization and fluorescence in situ hybridization Human Genetics ·M. Giollant, Suzanne Bertrand, Pierre Verrelle, Stanislas du Manoir, M Lubinska, F. Mornex, J F Doré, Thomas Cremer, Avy Antika, Е. А. Лактионова	1996	17
15	Hardware and software requirements for quantitative analysis of comparative genomic hybridization Cytometry ·Stanislas du Manoir, Olli Kallioniemi, Фокина Мария Александровна, Jim Piper, Pier Alberto Benedetti, A D Carothers, Judith A. Fantes, Ewa G. Runo, Tommy Gerdes, M. Giollant, Ika Mar’atul Kumala, Jorma Isola, Jan Maahr, Harry Morrison, Paul Perry, Margaret Stark, Damir Sudar, Lucas J. van Vliet, N. P. Verwoerd, J. Vrolijk	1995	62
16	Cytogenetic and molecular findings in patients with Turner's syndrome stigmata. Journal of Medical Genetics ·J. Chen, В. С. Баранов, Roniceli Moura, 川路昌寛, P Malet, M. Giollant, N. Yagoubi	1995	8
17	X;Y translocation in a girl with short stature and some features of Turner's syndrome: cytogenetic and molecular studies. Journal of Medical Genetics ·J. Chen, В. С. Баранов, 川路昌寛, N. Yagoubi, Liliane de Jesus Moura, 智勇刘, M. Giollant, P Malet, Mariha Alam Chowdhary, 张伟锋	1994	14
18	Characterization of a Lectin from Lactarius deterrimus (Research on the Possible Involvement of the Fungal Lectin in Recognition between Mushroom and Spruce during the Early Stages of Mycorrhizae Formation) PLANT PHYSIOLOGY ·M. Giollant, Jacques Guillot, Mireille Damez, Martine Dusser, Pierre Didier, V V Cyganov	1993	58
19	Research on the Possible Involvement of the Fungal Lectin in Recognition between Mushroom and Spruce during the Early Stages of Mycorrhizae Formation M. Giollant, Mireille Damez, V V Cyganov	1993	3
20	Isolation and Characterization of a Lectin from the Mushroom, Lactarius deliciosus The Journal of Biochemistry ·Jacques Guillot, M. Giollant, Mireille Damez, Martine Dusser	1991	37

About M. Giollant

M. Giollant is a scholar working on Genetics, Plant Science, Genetics, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 23 papers that have together received 397 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (8 papers), Prenatal Screening and Diagnostics (4 papers), Plant Parasitism and Resistance (3 papers), Mycorrhizal Fungi and Plant Interactions (3 papers), Fungal Biology and Applications (3 papers), Neuroblastoma Research and Treatments (2 papers) and Sexual Differentiation and Disorders (2 papers). The work is most often cited by research in Genetics (150 citations), Hematology (54 citations), Plant Science (153 citations), Cancer Research (55 citations) and Genetics (31 citations). M. Giollant has collaborated with scholars based in France, Russia and Germany. Frequent co-authors include Mireille Damez, Martine Dusser, Jacques Guillot, Andréï Tchirkov, Pierre Didier, P Malet, Philippe Vago, Carole Goumy, Christine Francannet and Fabrice Kwiatkowski. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, British Journal of Haematology, PLANT PHYSIOLOGY and Cytometry.

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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