I. Mahjneh

2.9k citations

36 papers · 1.9k indexed · 1 hit paper · h-index 18

Molecular Biology top 5%
Cellular and Molecular Neuroscience top 5%
Cardiology and Cardiovascular Medicine top 5%
Cell Biology top 5%
Physiology top 10%

Co-authors: Sharon Keers Kate Bushby Gianpiero Marconi Rumaisa Bashir Zohar Argov J. Beckmann S. Britton Isabelle Richard
Topics: Muscle Physiology and Disorders (20 papers)Genetic Neurodegenerative Diseases (10 papers)Cardiomyopathy and Myosin Studies (8 papers)
Cited by: Cellular and Molecular Neuroscience Cell Biology Molecular Biology
Journals: Nature Genetics Neurology The American Journal of Human Genetics
Partner nations: Finland United Kingdom Italy

In The Last Decade

I. Mahjneh

36 papers receiving 1.8k 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.

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

1998 526 citations Rumaisa Bashir, S. Britton et al. Nature Genetics profile →

Peers

Countries citing papers authored by I. Mahjneh

Since Specialization

Citations

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

Fields of papers citing papers by I. Mahjneh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. Mahjneh

This figure shows the co-authorship network connecting the top 25 collaborators of I. Mahjneh. A scholar is included among the top collaborators of I. Mahjneh 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 I. Mahjneh. I. Mahjneh 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	Dysregulated calcium homeostasis prevents plasma membrane repair in Anoctamin 5/TMEM16E-deficient patient muscle cells 2019 ·Cell Death Discovery ·Goutam Chandra,Aurélia Defour,(unknown),Kalpana Pandey,Soumya Ranjan Mishra,Vincent Mouly,(unknown),(unknown),I. Mahjneh,Hiroki Morizono,Nagarajan Pattabiraman,Anant K. Menon,Jyoti K. Jaiswal	30
2	DOK7 limb-girdle myasthenic syndrome mimicking congenital muscular dystrophy 2012 ·Neuromuscular Disorders ·I. Mahjneh,Hanns Lochmüller,Francesco Muntoni,Angela Abicht	24
3	Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus 2011 ·Neuromuscular Disorders ·Peter Hackman,Satu Sandell,J. Sarparanta,H. Luque,Sanna Huovinen,Johanna Palmio,Anders Paetau,Hannu Kalimo,I. Mahjneh,Bjarne Udd	16
4	Recessive Mutations in the Putative Calcium-Activated Chloride Channel Anoctamin 5 Cause Proximal LGMD2L and Distal MMD3 Muscular Dystrophies 2010 ·The American Journal of Human Genetics ·Véronique Bolduc,Gareth Marlow,Kym M. Boycott,(unknown),Hiroshi Inoue,J. Kroon,Mitsuo Itakura,Yves Robitaille,Lucie Parent,Frank Baas,Kuniko Mizuta,Nobuyuki Kamata,Isabelle Richard,Wim H.J.P. Linssen,I. Mahjneh,Marjolein Visser,Rumaisa Bashir,Bernard Brais	195
5	A new distal myopathy with mutation in anoctamin 5 2010 ·Neuromuscular Disorders ·I. Mahjneh,Jyoti K. Jaiswal,Antti Lamminen,Mirja Somer,Gareth Marlow,Sari Kiuru‐Enari,Rumaisa Bashir	50
6	Episodic muscle pain, stiffness, and weakness associated with tubular aggregates and myoedema 2007 ·European Journal of Neurology ·I. Mahjneh,Antti Lamminen,Hannu Tuominen	1
7	Human Balance Estimation using a Wireless 3D Acceleration Sensor Network 2006 ·PubMed ·Heidi Similä,(unknown),Mikko Lindholm,(unknown),I. Mahjneh	5
8	Patients with a Non‐dysferlin Miyoshi Myopathy have a Novel Membrane Repair Defect 2006 ·Traffic ·Jyoti K. Jaiswal,Gareth Marlow,(unknown),I. Mahjneh,(unknown),Maria Hill,Katsuya Miyake,Hannelore Haase,Louise V.B. Anderson,Isabelle Richard,Sari Kiuru‐Enari,Paul L. McNeil,Sanford M. Simon,Rumaisa Bashir	45
9	The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone 2005 ·Nature Genetics ·Anna‐Kaisa Anttonen,I. Mahjneh,Riikka H. Hämäläinen,Clotilde Lagier‐Tourenne,Outi Kopra,(unknown),Mikko Anttonen,Tarja Joensuu,Hannu Kalimo,Anders Paetau,Lisbeth Tranebjærg,Denys Chaigne,M. Kœnig,Orvar Eeg‐Olofsson,Bjarne Udd,Mirja Somer,Hannu Somer,Anna‐Elina Lehesjoki	160
10	Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophy 2004 ·Acta Neurologica Scandinavica ·I. Mahjneh,Antti Lamminen,(unknown),Anders Paetau,Peter Hackman,O Korhola,Hannu Somer	17
11	Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3) 2004 ·Neuromuscular Disorders ·Henna Haravuori,H. Annika Siitonen,I. Mahjneh,Peter Hackman,Laura Lahti,Hannu Somer,Leena Peltonen,Marjo Kestilä,Bjarne Udd	10
12	Pure quadriceps myopathy in two sisters 2003 ·European Journal of Neurology ·I. Mahjneh,Hannu Somer,Anders Paetau,Gianpiero Marconi	1
13	Axial myopathy - an unrecognised entity 2002 ·Journal of Neurology ·I. Mahjneh,Gianpiero Marconi,Anders Paetau,Antti Saarinen,Tapani Salmi,Hannu Somer	28
14	Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations 2001 ·Neuromuscular Disorders ·I. Mahjneh,Gianpiero Marconi,Kate Bushby,Louise V.B. Anderson,(unknown),Hannu Somer	63
15	Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) 2000 ·Neuromuscular Disorders ·Louise V.B. Anderson,(unknown),Robert Pogue,Elizabeth Vafiadaki,C. Pollitt,Keith Davison,Jennifer A. Moss,Sharon Keers,Angela Pyle,Pamela J. Shaw,I. Mahjneh,Zohar Argov,Cheryl R. Greenberg,Klaus Wrogemann,Tulio E. Bertorini,Hans H. Goebel,J. Beckmann,Rumaisa Bashir,Kate Bushby	113
16	Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development 1999 ·Human Molecular Genetics ·Louise V.B. Anderson,Kenneth Davison,Jessica Moss,C Young,Michael J. Cullen,John Walsh,Mary Ann Johnson,R. Bashir,S. Britton,Sharon Keers,Zohar Argov,I. Mahjneh,Françoise Fougerousse,J. Beckmann,K. Bushby	234
17	A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2Bbreakdown → 1998 ·Nature Genetics ·Rumaisa Bashir,S. Britton,Tom Strachan,Sharon Keers,Elizabeth Vafiadaki,Majlinda Lako,Isabelle Richard,Sylvie Marchand,Nathalie Bourg,Zohar Argov,Menachem Sadeh,I. Mahjneh,Gianpiero Marconi,Maria Rita Passos‐Bueno,Eloisa De Sá Moreira,Mayana Zatz,J. Beckmann,Kate Bushby	526
18	The molecular biology of LGMD2B — Towards the identification of the LGMD gene on chromosome 2p13 1996 ·Neuromuscular Disorders ·Kate Bushby,R. Bashir,Sharon Keers,S. Britton,Mayana Zatz,Maria-Rita Passos-Bueno,Michael Lovett,I. Mahjneh,Gianpiero Marconi,T Strachan	3
19	The phenotype of chromosome 2p-linked limb-girdle muscular dystrophy 1996 ·Neuromuscular Disorders ·I. Mahjneh,Maria-Rita Passos-Bueno,Mayana Zatz,Mariz Vainzof,Gianpiero Marconi,Lina Nashef,R. Bashir,Kate Bushby	39
20	Limb-girdle muscular dystrophy: a follow-up study of 79 patients 1996 ·Acta Neurologica Scandinavica ·I. Mahjneh,K. Bushby,A. Pizzi,R. Bashir,Gianpiero Marconi	17

About I. Mahjneh

I. Mahjneh is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology, having authored 36 papers that have together received 1.9k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (20 papers), Genetic Neurodegenerative Diseases (10 papers) and Cardiomyopathy and Myosin Studies (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (522 citations), Cell Biology (401 citations) and Molecular Biology (1.7k citations). I. Mahjneh has collaborated with scholars based in Finland, United Kingdom and Italy. Frequent co-authors include Sharon Keers, Kate Bushby, Gianpiero Marconi, Rumaisa Bashir, Zohar Argov, J. Beckmann, S. Britton, Isabelle Richard, Louise V.B. Anderson and Elizabeth Vafiadaki. Their work appears in journals such as Nature Genetics, Neurology and The American Journal of Human 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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