Anas M. Khanshour

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 14 papers. Top paper: “Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis”.

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis

eLife(2023)10.7554/elife.89762

N/A

0.216DataRank · unranked

3 citations

Anas M. Khanshour, Aki Ushiki, Nao Otomo, Yoshinao Koike, Elísabet Einarsdóttir +20 more

Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice

Journal of Bone and Mineral Research(2020)10.1002/jbmr.4323

N/A

0DataRank · unranked

11 citations

Kristin Denton, Jamie L. Russell, Julia Kozlitina, Carlos R. Ferreira, Amy Feldman Lewanda +18 more

Genetic association and characterization ofFSTL5in isolated clubfoot

Human Molecular Genetics(2020)10.1093/hmg/ddaa236

N/A

0DataRank · unranked

10 citations

Yared H. Kidane, Julia Kozlitina, Reuel Cornelia, Alexandra Rafipay, Vanessa D. de Mello +13 more

Novel homozygous variant in WISP3 in a family with unrecognized progressive pseudorheumatoid dysplasia

Clinical Case Reports(2020)10.1002/ccr3.2884

N/A

0DataRank · unranked

1 citations

Anas M. Khanshour, David Wilkes, Jonathan J. Rios, Kelly Sheff, Lorien Nassi +2 more

Impaired glycine neurotransmission causes adolescent idiopathic scoliosis

Journal of Clinical Investigation(2023)10.1172/jci168783

N/A

0DataRank · unranked

32 citations

Ming Yue, Jason Pui Yin Cheung, Prudence Wing Hang Cheung, Yanhui Fan, Meicheng Wu +21 more

Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study

Frontiers in Endocrinology(2023)10.3389/fendo.2023.1089414

N/A

0DataRank · unranked

9 citations

Anas M. Khanshour, Masaru Koido, Kazuki Takeda, Yukihide Momozawa, Michiaki Kubo +43 more

Interrogating Causal Effects of Body Composition and Puberty‐Related Risk Factors on Adolescent Idiopathic Scoliosis: A Two‐Sample Mendelian Randomization Study

JBMR Plus(2023)10.1002/jbm4.10830

N/A

0DataRank · unranked

7 citations

Nao Otomo, Isabel Gamache, Takuro Iwami, Yoshinao Koike, Anas M. Khanshour +5 more

RAB1A haploinsufficiency phenocopies the 2p14–p15 microdeletion and is associated with impaired neuronal differentiation

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.009

N/A

0DataRank · unranked

4 citations

Yang Li, Nandina Paria, Ryan J. Bohlender, Chad Huff, Jill A. Rosenfeld +17 more

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.26.542293

N/A

0DataRank · unranked

1 citations

Anas M. Khanshour, Aki Ushiki, Nao Otomo, Yoshinao Koike, Elísabet Einarsdóttir +20 more

Association of an estrogen-sensitive Pax1-Col11a1-Mmp3 signaling axis with adolescent idiopathic scoliosis

(2023)10.7554/elife.89762.1

N/A

0DataRank · unranked

0 citations

Anas M. Khanshour, Aki Ushiki, Nao Otomo, Yoshinao Koike, Elísabet Einarsdóttir +20 more

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis

eLife(2024)10.7554/elife.89762.4

N/A

0DataRank · unranked

6 citations

Anas M. Khanshour, Aki Ushiki, Nao Otomo, Yoshinao Koike, Elísabet Einarsdóttir +20 more

Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101958

N/A

0DataRank · unranked

3 citations

Katie A. Ashton, Lachlan De Hayr, K.T. Lee, Omkar L. Patkar, Emma Krzesinski +15 more

The cartilage matrisome in adolescent idiopathic scoliosis

Bone Research(2020)10.1038/s41413-020-0089-0

N/A

0DataRank · unranked

65 citations

Diane S. Sepich, Aki Ushiki, Anas M. Khanshour, Yared H. Kidane, Nadja Makki +6 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more