Masaki Takagi

750 citations

54 papers · 514 indexed · h-index 14

Genetics top 10%
Molecular Biology
Endocrinology, Diabetes and Metabolism top 10%
Rheumatology
Oncology

Co-authors: Tomonobu Hasegawa Yukihiro Hasegawa Satoshi Narumi Gen Nishimura Tomohiro Ishii Ryuji Fukuzawa Naoko Amano K Miyai
Topics: Connective tissue disorders research (20 papers)Bone health and treatments (8 papers)Neurogenetic and Muscular Disorders Research (7 papers)
Cited by: Genetics Endocrinology, Diabetes and Metabolism Nephrology
Journals: PLoS ONE European Journal of Endocrinology Thyroid
Partner nations: Japan United States India

In The Last Decade

Masaki Takagi

54 papers receiving 510 citations

Peers

Countries citing papers authored by Masaki Takagi

Since Specialization

Citations

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

Fields of papers citing papers by Masaki Takagi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masaki Takagi

This figure shows the co-authorship network connecting the top 25 collaborators of Masaki Takagi. A scholar is included among the top collaborators of Masaki Takagi 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 Masaki Takagi. Masaki Takagi 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	Double non-contiguous fractures in a patient with spondylo-epiphyseal dysplasia with spinal ankylosis treated with open and percutaneous spinal fixation technique: a case report 2018 ·BMC Research Notes ·(unknown),Kenichi Kawaguchi,Tadashi Matsumoto,Masaki Takagi,Tatsuro Kondoh,Gen Nishimura,Aritoshi Iida,Shiro Ikegawa,Nobuhiko Haga,Go Kato	2
2	Novel compound heterozygous mutations identified by whole exome sequencing in a Japanese patient with geroderma osteodysplastica 2017 ·European Journal of Medical Genetics ·(unknown),Masaki Takagi,(unknown),(unknown),Satoshi Narumi,Tomonobu Hasegawa,Gen Nishimura,Hiroshi Yoshihashi	6
3	Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield syndrome 2016 ·Human Genome Variation ·Masaki Takagi,Tatsuya Miyoshi,(unknown),(unknown),(unknown),Ryuji Fukuzawa,Tomonobu Hasegawa	9
4	Criteria for radiologic diagnosis of hypochondroplasia in neonates 2016 ·Pediatric Radiology ·Tomoko Saito,Keisuke Nagasaki,Gen Nishimura,Masaki Wada,Hiromi Nyuzuki,Masaki Takagi,Tomonobu Hasegawa,Naoko Amano,Jun Murotsuki,Hideaki Sawai,Takahiro Yamada,(unknown),Akihiko Saitoh	7
5	TmP/GFR is a Useful Marker in Making a Clinical Diagnosis of X-Linked Hypophosphataemic Rickets Caused by the PHEX Gene Mutation 2015 ·(unknown),K Miyai,Masaki Takagi,Masahiro Goto,(unknown),(unknown),(unknown),(unknown),(unknown),Yukihiro Hasegawa	2
6	Functional Characterization of c.870+3_6delGAGT Splice Site Mutation in <b><i>NR5A1</i></b> 2015 ·Hormone Research in Paediatrics ·Masaki Takagi,(unknown),(unknown),Yukihiro Hasegawa	2
7	A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of sotos syndrome 2015 ·American Journal of Medical Genetics Part A ·(unknown),Masaki Takagi,Hiroshi Yoshihashi,Masaru Miura,Satoshi Narumi,Tomonobu Hasegawa,(unknown),Yukihiro Hasegawa	10
8	Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger 2015 ·Pediatric Radiology ·(unknown),Masaki Takagi,Yukihiro Hasegawa,Hülya Kayserili,Gen Nishimura	6
9	Heterozygous defects in PAX6 gene and congenital hypopituitarism 2014 ·European Journal of Endocrinology ·Masaki Takagi,Keisuke Nagasaki,Ikuma Fujiwara,Tomohiro Ishii,Naoko Amano,Yumi Asakura,Koji Muroya,Yukihiro Hasegawa,Masanori Adachi,Tomonobu Hasegawa	17
10	Osteogenesis imperfecta IIC caused by a novel heterozygous mutation in the C-propeptide region of COL1A1 2014 ·Human Genome Variation ·Masaki Takagi,M. Matsushita,Gen Nishimura,Tomonobu Hasegawa	4
11	Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature 2014 ·European Journal of Pediatrics ·Taichi Kitaoka,Yoko Miyoshi,Noriyuki Namba,Kohji Miura,Takuo Kubota,Yasuhisa Ohata,Makoto Fujiwara,Masaki Takagi,Tomonobu Hasegawa,Harald Jüppner,Keiichi Ozono	9
12	A 2.0 Mb microdeletion in proximal chromosome 14q12, involving regulatory elements of FOXG1, with the coding region of FOXG1 being unaffected, results in severe developmental delay, microcephaly, and hypoplasia of the corpus callosum 2013 ·European Journal of Medical Genetics ·Masaki Takagi,Goro Sasaki,(unknown),(unknown),Yoko Tanaka,Tomonobu Hasegawa	13
13	A novel mutation in SOX3 polyalanine tract: a case of kabuki syndrome with combined pituitary hormone deficiency harboring double mutations in MLL2 and SOX3 2013 ·Pituitary ·Masaki Takagi,Tomohiro Ishii,Chiharu Torii,Kenjiro Kosaki,Tomonobu Hasegawa	18
14	Recurrence of osteogenesis imperfecta due to maternal mosaicism of a novel COL1A1 mutation 2012 ·American Journal of Medical Genetics Part A ·Takahiro Yamada,Masaki Takagi,Gen Nishimura,Rina Akaishi,Itsuko Furuta,Mamoru Morikawa,Takashi Yamada,Kazutoshi Cho,Hideaki Sawai,Shiro Ikegawa,Tomonobu Hasegawa,Hisanori Minakami	1
15	Radiological clues to the early diagnosis of hypochondroplasia in the neonatal period: Report of two patients 2012 ·American Journal of Medical Genetics Part A ·Tomoko Saito,Keisuke Nagasaki,Gen Nishimura,Masaki Takagi,Tomonobu Hasegawa,Makoto Uchiyama	9
16	A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta 2012 ·PLoS ONE ·Masaki Takagi,Tomohiro Ishii,Aileen M. Barnes,MaryAnn Weis,Naoko Amano,Mamoru Tanaka,Ryuji Fukuzawa,Gen Nishimura,David R. Eyre,Joan C. Marini,Tomonobu Hasegawa	27
17	Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism 2012 ·PLoS ONE ·Masaki Takagi,Tomohiro Ishii,Mikako Inokuchi,Naoko Amano,Satoshi Narumi,Yumi Asakura,Koji Muroya,Yukihiro Hasegawa,Masanori Adachi,Tomonobu Hasegawa	22
18	A family of pseudohypoparathyroidism type Ia with an 850‐kb submicroscopic deletion encompassing the whole GNAS locus 2011 ·American Journal of Medical Genetics Part A ·(unknown),Keisuke Nagasaki,Masaki Takagi,Satoshi Narumi,Tomohiro Ishii,Tomonobu Hasegawa	19
19	Heterozygous C‐propeptide mutations in COL1A1: Osteogenesis imperfecta type IIC and dense bone variant 2011 ·American Journal of Medical Genetics Part A ·Masaki Takagi,Naoaki Hori,Yasutsugu Chinen,Kenji Kurosawa,Yukichi Tanaka,(unknown),(unknown),Ryuji Fukuzawa,Gen Nishimura,Jürgen W. Spranger,Tomonobu Hasegawa	7
20	Late manifestations of tricho‐rhino‐pharangeal syndrome in a patient: Expanded skeletal phenotype in adulthood 2010 ·American Journal of Medical Genetics Part A ·Kosuke Izumi,Masaki Takagi,Aditi Shah Parikh,(unknown),(unknown),Gen Nishimura,Chiharu Torii,Kenjiro Kosaki,Tomonobu Hasegawa,Derek Neilson	11

About Masaki Takagi

Masaki Takagi is a scholar working on Genetics, Genetics and Rheumatology, having authored 54 papers that have together received 514 indexed citations. Recurring topics across this work include Connective tissue disorders research (20 papers), Bone health and treatments (8 papers) and Neurogenetic and Muscular Disorders Research (7 papers). The work is most often cited by research in Genetics (290 citations), Endocrinology, Diabetes and Metabolism (141 citations) and Nephrology (43 citations). Masaki Takagi has collaborated with scholars based in Japan, United States and India. Frequent co-authors include Tomonobu Hasegawa, Yukihiro Hasegawa, Satoshi Narumi, Gen Nishimura, Tomohiro Ishii, Ryuji Fukuzawa, Naoko Amano, K Miyai, Keisuke Nagasaki and Masanori Adachi. Their work appears in journals such as PLoS ONE, European Journal of Endocrinology and Thyroid.

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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