Citation Impact
Citing Papers
Characterizing and explaining the impact of disease-associated mutations in proteins without known structures or structural homologs
2022 StandoutNobel
Denisovan ancestry and population history of early East Asians
2020 StandoutScienceNobel
Identification of a new hominin bone from Denisova Cave, Siberia using collagen fingerprinting and mitochondrial DNA analysis
2016 StandoutNobel
The genome of the offspring of a Neanderthal mother and a Denisovan father
2018 StandoutNatureNobel
Direct radiocarbon dating and DNA analysis of the Darra-i-Kur (Afghanistan) human temporal bone
2017 StandoutNobel
Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer
2015 Standout
STRA6 is critical for cellular vitamin A uptake and homeostasis
2014
The single-cell transcriptional landscape of mammalian organogenesis
2019 StandoutNature
Enhancer redundancy provides phenotypic robustness in mammalian development
2018 Nature
Hypoxia-inducible factors promote breast cancer stem cell specification and maintenance in response to hypoxia or cytotoxic chemotherapy
2018 StandoutNobel
The earliest Denisovans and their cultural adaptation
2021 StandoutNobel
Nuclear DNA sequences from the Middle Pleistocene Sima de los Huesos hominins
2016 StandoutNatureNobel
Mutations in the noncoding genome
2015
Structure of the STRA6 receptor for retinol uptake
2016 StandoutScienceNobel
Reducing Microbial and Human Contamination in DNA Extractions from Ancient Bones and Teeth
2015
A fourth Denisovan individual
2017 StandoutNobel
A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome
2015
A high-coverage Neandertal genome from Chagyrskaya Cave
2020 StandoutNobel
Palaeoproteomic evidence identifies archaic hominins associated with the Châtelperronian at the Grotte du Renne
2016 StandoutNobel
Direct dating of Neanderthal remains from the site of Vindija Cave and implications for the Middle to Upper Paleolithic transition
2017 StandoutNobel
Works of Morad Ansari being referenced
Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects
2014
Variant detection sensitivity and biases in whole genome and exome sequencing
2014
Identification of Novel Craniofacial Regulatory Domains Located far Upstream ofSOX9and Disrupted in Pierre Robin Sequence
2014
Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center
2013