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Subject Areas on Research
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A competitive nonverbal false belief task for children and apes.
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A fruit in the hand or two in the bush? Divergent risk preferences in chimpanzees and bonobos.
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Abundant gene conversion between arms of palindromes in human and ape Y chromosomes.
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All great ape species (Gorilla gorilla, Pan paniscus, Pan troglodytes, Pongo abelii) and two-and-a-half-year-old children (Homo sapiens) discriminate appearance from reality.
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All great ape species follow gaze to distant locations and around barriers.
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Apes reciprocate food positively and negatively.
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Apes' and children's understanding of cooperative and competitive motives in a communicative situation.
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Apes' use of iconic cues in the object-choice task.
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Assessing conservation attitudes and behaviors of Congolese children neighboring the world's first bonobo (Pan paniscus) release site.
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Body language: The interplay between positional behavior and gestural signaling in the genus Pan and its implications for language evolution.
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Body orientation and face orientation: two factors controlling apes' behavior from humans.
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Bonobo but not chimpanzee infants use socio-sexual contact with peers.
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Bonobos Prefer Individuals that Hinder Others over Those that Help.
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Bonobos and chimpanzees exhibit human-like framing effects.
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Bonobos exhibit delayed development of social behavior and cognition relative to chimpanzees.
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Bonobos have a more human-like second-to-fourth finger length ratio (2D:4D) than chimpanzees: a hypothesized indication of lower prenatal androgens.
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Bonobos respond prosocially toward members of other groups.
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Bonobos share with strangers.
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Bonobos voluntarily share their own food with others.
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Children, chimpanzees, and bonobos adjust the visibility of their actions for cooperators and competitors.
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Chimpanzees and bonobos distinguish between risk and ambiguity.
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Chimpanzees and bonobos exhibit divergent spatial memory development.
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Chimpanzees and bonobos exhibit emotional responses to decision outcomes.
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Chimpanzees, bonobos, and children successfully coordinate in conflict situations.
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Communication about absent entities in great apes and human infants.
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Differences in the cognitive skills of bonobos and chimpanzees.
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Differences in the early cognitive development of children and great apes.
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Differences in the nonverbal requests of great apes and human infants.
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Different ontogenetic patterns of testosterone production reflect divergent male reproductive strategies in chimpanzees and bonobos.
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Differential changes in steroid hormones before competition in bonobos and chimpanzees.
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Direct and indirect reputation formation in nonhuman great apes (Pan paniscus, Pan troglodytes, Gorilla gorilla, Pongo pygmaeus) and human children (Homo sapiens).
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Does sympathy motivate prosocial behaviour in great apes?
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Evolution of ASPM coding variation in apes and associations with brain structure in chimpanzees.
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Evolution of water conservation in humans.
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FOXP2 variation in great ape populations offers insight into the evolution of communication skills.
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Fiber-type phenotype of the jaw-closing muscles in Gorilla gorilla, Pan troglodytes, and Pan paniscus: A test of the Frequent Recruitment Hypothesis.
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Gestural communication in subadult bonobos (Pan paniscus): repertoire and use.
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Great ape genetic diversity and population history.
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Great apes and human children rationally monitor their decisions.
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Great apes anticipate that other individuals will act according to false beliefs.
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Great apes distinguish true from false beliefs in an interactive helping task.
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Lethal aggression in Pan is better explained by adaptive strategies than human impacts.
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Making inferences about the location of hidden food: social dog, causal ape.
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Males with a mother living in their group have higher paternity success in bonobos but not chimpanzees.
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Metabolic acceleration and the evolution of human brain size and life history.
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Predicting body mass of bonobos (Pan paniscus) with human-based morphometric equations.
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Psychological health of orphan bonobos and chimpanzees in African sanctuaries.
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Ratcheting up the ratchet: on the evolution of cumulative culture.
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Reaching around barriers: the performance of the great apes and 3-5-year-old children.
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Reliance on head versus eyes in the gaze following of great apes and human infants: the cooperative eye hypothesis.
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Spontaneous triadic engagement in bonobos (Pan paniscus) and chimpanzees (Pan troglodytes).
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The Pan social brain: An evolutionary history of neurochemical receptor genes and their potential impact on sociocognitive differences.
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The development and flexibility of gaze alternations in bonobos and chimpanzees.
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The evolutionary origins of human patience: temporal preferences in chimpanzees, bonobos, and human adults.
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The foot of Homo naledi.
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The hand of Homo naledi.
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The ontogenetic ritualization of bonobo gestures.
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Theft in an ultimatum game: chimpanzees and bonobos are insensitive to unfairness.
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Tolerance allows bonobos to outperform chimpanzees on a cooperative task.
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Visually attending to a video together facilitates great ape social closeness.
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Warlike chimpanzees and peacemaking bonobos.
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What's in a frame? Response to Kanngiesser & Woike (2016).