Michael A. Morris

7.7k total citations
118 papers, 4.8k citations indexed

About

Michael A. Morris is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Michael A. Morris has authored 118 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 39 papers in Genetics and 26 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Michael A. Morris's work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (11 papers) and Cystic Fibrosis Research Advances (10 papers). Michael A. Morris is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (11 papers) and Cystic Fibrosis Research Advances (10 papers). Michael A. Morris collaborates with scholars based in Switzerland, United States and United Kingdom. Michael A. Morris's co-authors include Stylianos E. Antonarakis, Arnaud Gos, Colette Rossier, Marguerite Neerman‐Arbez, Virginia K. Lasseter, Gerald Nestadt, Paula Wolyniec, Maria Karayiorgou, Maria D. Lalioti and Armand Bottani and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Michael A. Morris

117 papers receiving 4.6k citations

Peers

Countries citing papers authored by Michael A. Morris

Since Specialization

Citations

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

Fields of papers citing papers by Michael A. Morris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael A. Morris. 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 Michael A. Morris. The network helps show where Michael A. Morris may publish in the future.

Co-authorship network of co-authors of Michael A. Morris

This figure shows the co-authorship network connecting the top 25 collaborators of Michael A. Morris. A scholar is included among the top collaborators of Michael A. Morris 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 Michael A. Morris. Michael A. Morris 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	Impact of Clinical Factors on 18F-Flotufolastat Detection Rates in Men With Recurrent Prostate Cancer: Exploratory Analysis of the Phase 3 SPOTLIGHT Study 2024 ·Advances in Radiation Oncology ·Benjamin Lowentritt, Ashesh B. Jani, Brian T. Helfand, Edward Uchio, Michael A. Morris, (unknown), Albert Chau, (unknown), Brian F. Chapin, David M. Schuster	4
2	The role of the Genetic Counsellor in the multidisciplinary team: the perception of geneticists in Europe 2022 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Alessandra Renieri, Francesca Mari, Michael A. Morris, Christophe Cordier	11
3	MECP2 duplication syndrome in a patient from Cameroon 2020 ·American Journal of Medical Genetics Part A ·Cedrik Tekendo‐Ngongang, Sophie Dahoun, Séraphin Nguefack, Isabelle Moix, Stefania Gimelli, (unknown), Michael A. Morris, Frédérique Sloan‐Béna, Ambroise Wonkam	5
4	Increased Prevalence of NLRP3 Q703K Variant Among Patients With Autoinflammatory Diseases: An International Multicentric Study 2020 ·Frontiers in Immunology ·Katerina Theodoropoulou, Helmut Wittkowski, Nathalie Busso, Annette von Scheven-Gête, Isabelle Moix, Federica Vanoni, (unknown), Gerd Horneff, Johannes‐Peter Haas, Nadine Fischer, (unknown), Rainer Berendes, Georg Heubner, Annette Jansson, Elke Lainka, Annette Leimgruber, Michael A. Morris, Dirk Foell, Michaël Hofer	16
5	Initiation of a medical genetics service in sub-Saharan Africa: Experience of prenatal diagnosis in Cameroon 2011 ·European Journal of Medical Genetics ·Ambroise Wonkam, Cedrik Tekendo‐Ngongang, (unknown), (unknown), Sophie Dahoun, Frédérique Béna, Michael A. Morris	36
6	[R74W;R1070W;D1270N]: A new complex allele responsible for cystic fibrosis 2010 ·Journal of Cystic Fibrosis ·(unknown), (unknown), (unknown), J. Beckmann, Michael A. Morris, Gaudenz Hafen, Florence Fellmann	6
7	Elicited repetitive daily blindness 2009 ·Neurology ·Katayoun Vahedi, Christel Depienne, (unknown), Florence Riant, (unknown), Oriane Trouillard, Alain Gaudric, Michael A. Morris, Eric Leguern, Elisabeth Tournier‐Lasserve, (unknown)	66
8	A rapid and accurate approach to identify single nucleotide polymorphisms of mitochondrial DNA using MALDI-TOF mass spectrometry 2008 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·Alex Xiu‐Cheng Fan, Henk Garritsen, Shereen El Tarhouny, Michael A. Morris, Sinuhe Hahn, Wolfgang Holzgreve, Xiao Yan Zhong	22
9	Subtelomeric 6p deletion: Clinical and array‐CGH characterization in two patients 2008 ·American Journal of Medical Genetics Part A ·Danielle Martinet, Isabel Filges, (unknown), Michael A. Morris, (unknown), Sophie Dahoun, Armand Bottani, Marie‐Claude Addor, Stylianos E. Antonarakis, J. Beckmann, Frédérique Béna	27
10	No Evidence for an Effect of COMT Val158Met Genotype on Executive Function in Patients With 22q11 Deletion Syndrome 2006 ·American Journal of Psychiatry ·Bronwyn Glaser, Martin Debbané, Christine Hinard, Michael A. Morris, Sophie Dahoun, Stylianos E. Antonarakis, Stéphan Eliez	37
11	Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapes 2005 ·Nature Genetics ·François Spitz, (unknown), Michael A. Morris, Denis Duboule	120
12	A SEM study of tooth morphology using high kV and back scattered electron imaging technique 2001 ·Journal of Dental Research ·(unknown), Hien Chi Ngo, G. H. Mount, Michael A. Morris, Carol J. Baker	2
13	Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes 2001 ·Human Genetics ·Marguerite Neerman‐Arbez, Philippe de Moerloose, (unknown), (unknown), (unknown), Christine A. Biron, Jeanne‐Yvonne Borg, Stefan Eber, Esther Meili, (unknown), Laurent Ripoll, C. Vervel, (unknown), Philippe Staeger, Stylianos E. Antonarakis, Michael A. Morris	56
14	Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia. 2000 ·Blood ·Marguerite Neerman‐Arbez, Philippe de Moerloose, Claire Bridel, (unknown), (unknown), Colette Rossier, Kathelijne Peerlinck, S. Claeyssens, (unknown), Roseline d’Oiron, Marie Dreyfus, (unknown), (unknown), Stylianos E. Antonarakis, Michael A. Morris	77
15	The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster 1999 ·European Journal of Human Genetics ·Marguerite Neerman‐Arbez, Stylianos E. Antonarakis, (unknown), Michael A. Morris	23
16	A testis-specific gene, TPTE , encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y 1999 ·Human Genetics ·Haiming Chen, Colette Rossier, Michael A. Morris, Hamish S. Scott, Arnaud Gos, Amos Bairoch, Stylianos E. Antonarakis	63
17	A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype 1997 ·Human Genetics ·Martin Hergersberg, (unknown), Thomas Bettecken, (unknown), (unknown), (unknown), (unknown), Sabina Liechti‐Gallati, Michael A. Morris, Daniel F. Schorderet, (unknown), Hans Moser, Naseem Malik	11
18	Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping. 1996 ·Genome Research ·Haiming Chen, Roman Chrast, Colette Rossier, Michael A. Morris, Maria D. Lalioti, Stylianos E. Antonarakis	49
19	Exon skipping associated with A→G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene 1994 ·Human Molecular Genetics ·Pierre Hutter, Stylianos E. Antonarakis, (unknown), Michael A. Morris	7
20	Some of the applications for polymer grids in concrete 1987 ·Concrete ·Michael A. Morris	11

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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