Michael F. Buckley

Biochemistry, Genetics and Molecular Biology

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 6 papers. Top paper: “FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women”.

FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

European Journal of Human Genetics(2023)10.1038/s41431-022-01257-w

N/A

0.406DataRank · unranked

14 citations

Amandine Billaud, Thomas U. Ahearn, Natalia Antonenkova, Heiko Becher, Matthias W. Beckmann +95 more

The impact of coding germline variants on contralateral breast cancer risk and survival

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.02.003

N/A

0DataRank · unranked

27 citations

Nasim Mavaddat, Taru Muranen, Thomas U. Ahearn, Jamie Allen, Irene L. Andrulis +94 more

Dominant-negative variants in CBX1 cause a neurodevelopmental disorder

Genetics in Medicine(2023)10.1016/j.gim.2023.100861

N/A

0DataRank · unranked

7 citations

Aiko Iwata‐Otsubo, Kerith‐Rae Dias, Suzanna E.L. Temple, Koji Nagao, Lachlan De Hayr +28 more

Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.01.006

N/A

0DataRank · unranked

6 citations

Marisol Cortés, Periklis Makrythanasis, Mohnish Suri, Alexander M. Taylor, Jennifer A. Sullivan +44 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

Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.004

N/A

0DataRank · unranked

8 citations

Kyriaki Michailidou, Michael T. Parsons, Cristina Fortuño, Manjeet K. Bolla, Qin Wang +95 more