Masaki Takagi

750 citations

54 papers · 514 indexed · h-index 14

Genetics top 10%
- Connective tissue disorders research 20
- Neurogenetic and Muscular Disorders Research 7
- Genetics and Neurodevelopmental Disorders 6
- Genetic Syndromes and Imprinting 5
- Genomic variations and chromosomal abnormalities 5
Endocrinology, Diabetes and Metabolism top 10%
Nephrology top 10%
Rheumatology
- Bone and Dental Protein Studies 6
Molecular Biology
- Fibroblast Growth Factor Research 4
Oncology
- Bone health and treatments 8

Co-authors: Tomonobu Hasegawa Yukihiro Hasegawa Satoshi Narumi Gen Nishimura Tomohiro Ishii Ryuji Fukuzawa Naoko Amano K Miyai
Cited by: Genetics Endocrinology, Diabetes and Metabolism Nephrology
Journals: Hormone Research in Paediatrics (3 papers)European Journal of Medical Genetics (2 papers)European Journal of Endocrinology (2 papers)
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

The 25 scholars most cited alongside Masaki Takagi, 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 Masaki Takagi Line = papers co-authored together Masaki Takagi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
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 BMC Research Notes ·T. John,Kenichi Kawaguchi,Tadashi Matsumoto,Masaki Takagi,Tatsuro Kondoh,Gen Nishimura,Aritoshi Iida,Shiro Ikegawa,Nobuhiko Haga,Go Kato	2018	2
2	Novel compound heterozygous mutations identified by whole exome sequencing in a Japanese patient with geroderma osteodysplastica European Journal of Medical Genetics ·Jeffery A Scott,Masaki Takagi,弘行藤井,E. Gugenhan,Satoshi Narumi,Tomonobu Hasegawa,Gen Nishimura,Hiroshi Yoshihashi	2017	6
3	Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield syndrome Human Genome Variation ·Masaki Takagi,Tatsuya Miyoshi,Merhawi Wells-Bogue,V.V. Telny,M. Bonsembiante,Ryuji Fukuzawa,Tomonobu Hasegawa	2016	9
4	Criteria for radiologic diagnosis of hypochondroplasia in neonates Pediatric Radiology ·Tomoko Saito,Keisuke Nagasaki,Gen Nishimura,Masaki Wada,Hiromi Nyuzuki,Masaki Takagi,Tomonobu Hasegawa,Naoko Amano,Jun Murotsuki,Hideaki Sawai,Takahiro Yamada,Changsig Kong,Akihiko Saitoh	2016	7
5	TmP/GFR is a Useful Marker in Making a Clinical Diagnosis of X-Linked Hypophosphataemic Rickets Caused by the PHEX Gene Mutation Jeffery A Scott,K Miyai,Masaki Takagi,Masahiro Goto,Jos eacute Kuhn Odair,Sukmah Mahesha Dyah,力也山室,松浦検校,Christine Knebusch,Yukihiro Hasegawa	2015	2
6	Functional Characterization of c.870+3_6delGAGT Splice Site Mutation in <b><i>NR5A1</i></b> Hormone Research in Paediatrics ·Masaki Takagi,B. Cordiani,M. Bonsembiante,Yukihiro Hasegawa	2015	2
7	A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of sotos syndrome American Journal of Medical Genetics Part A ·Christine Knebusch,Masaki Takagi,Hiroshi Yoshihashi,Masaru Miura,Satoshi Narumi,Tomonobu Hasegawa,Arganini,Yukihiro Hasegawa	2015	10
8	Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger Pediatric Radiology ·M. Bonsembiante,Masaki Takagi,Yukihiro Hasegawa,Hülya Kayserili,Gen Nishimura	2015	6
9	Heterozygous defects in PAX6 gene and congenital hypopituitarism European Journal of Endocrinology ·Masaki Takagi,Keisuke Nagasaki,Ikuma Fujiwara,Tomohiro Ishii,Naoko Amano,Yumi Asakura,Koji Muroya,Yukihiro Hasegawa,Masanori Adachi,Tomonobu Hasegawa	2014	17
10	Osteogenesis imperfecta IIC caused by a novel heterozygous mutation in the C-propeptide region of COL1A1 Human Genome Variation ·Masaki Takagi,M. Matsushita,Gen Nishimura,Tomonobu Hasegawa	2014	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 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	2014	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 European Journal of Medical Genetics ·Masaki Takagi,Goro Sasaki,Gorbovskii A.I.,Ciaran Lyons,Yoko Tanaka,Tomonobu Hasegawa	2013	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 Pituitary ·Masaki Takagi,Tomohiro Ishii,Chiharu Torii,Kenjiro Kosaki,Tomonobu Hasegawa	2013	18
14	Recurrence of osteogenesis imperfecta due to maternal mosaicism of a novel COL1A1 mutation 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	2012	1
15	Radiological clues to the early diagnosis of hypochondroplasia in the neonatal period: Report of two patients American Journal of Medical Genetics Part A ·Tomoko Saito,Keisuke Nagasaki,Gen Nishimura,Masaki Takagi,Tomonobu Hasegawa,Makoto Uchiyama	2012	9
16	A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta 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	2012	27
17	Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism PLoS ONE ·Masaki Takagi,Tomohiro Ishii,Mikako Inokuchi,Naoko Amano,Satoshi Narumi,Yumi Asakura,Koji Muroya,Yukihiro Hasegawa,Masanori Adachi,Tomonobu Hasegawa	2012	22
18	A family of pseudohypoparathyroidism type Ia with an 850‐kb submicroscopic deletion encompassing the whole GNAS locus American Journal of Medical Genetics Part A ·Gorbovskii A.I.,Keisuke Nagasaki,Masaki Takagi,Satoshi Narumi,Tomohiro Ishii,Tomonobu Hasegawa	2011	19
19	Heterozygous C‐propeptide mutations in COL1A1: Osteogenesis imperfecta type IIC and dense bone variant American Journal of Medical Genetics Part A ·Masaki Takagi,Naoaki Hori,Yasutsugu Chinen,Kenji Kurosawa,Yukichi Tanaka,Shaheed Mahr,Ximena Celi Loaiza,Ryuji Fukuzawa,Gen Nishimura,Jürgen W. Spranger,Tomonobu Hasegawa	2011	7
20	Late manifestations of tricho‐rhino‐pharangeal syndrome in a patient: Expanded skeletal phenotype in adulthood American Journal of Medical Genetics Part A ·Kosuke Izumi,Masaki Takagi,Aditi Shah Parikh,Pellet Sandra,Sifa Nayihiki,Gen Nishimura,Chiharu Torii,Kenjiro Kosaki,Tomonobu Hasegawa,Derek Neilson	2010	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), Neurogenetic and Muscular Disorders Research (7 papers), Bone and Dental Protein Studies (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genetic Syndromes and Imprinting (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Fibroblast Growth Factor Research (4 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 Hormone Research in Paediatrics, European Journal of Medical Genetics, European Journal of Endocrinology, PLoS ONE and American Journal of Medical Genetics Part A.

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