Increased affiliative response to vasopressin in mice expressing the V1a receptor from a monogamous vole

A role for central vasopressin in pair bonding in monogamous prairie voles

Winslow, J. T., Hastings, N., Carter, C. S., Harbaugh, C. R., & Insel, T. R. (1993) · Nature · doi:10.1038/365545a0 · Cited by 948

Vasopressin/serotonin interactions in the anterior hypothalamus control aggressive behavior in golden hamsters

Ferris, C. F., Melloni Jr, R. H., Koppel, G., Perry, K. W., Fuller, R. W., & Delville, Y. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04331.1997 · Cited by 495

Patterns of brain vasopressin receptor distribution associated with social organization in microtine rodents

Insel, T., Wang, Z., & Ferris, C. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-09-05381.1994 · Cited by 454

Vasopressin and oxytocin receptors in the central nervous system

Tribollet, E., & Barberis, C. (1996) · Critical Reviews™ in Neurobiology · doi:10.1615/critrevneurobiol.v10.i1.60 · Cited by 399

Role of septal vasopressin innervation in paternal behavior in prairie voles (Microtus ochrogaster).

Wang, Z., Ferris, C. F., & De Vries, G. J. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.1.400 · Cited by 381

Reduced androgen receptor gene expression with first exon CAG repeat expansion.

Choong, C. S. Y., Kemppainen, J. A., Zhou, Z., & Wilson, E. M. (1996) · Molecular Endocrinology · doi:10.1210/mend.10.12.8961263 · Cited by 327

Species Differences in Paternal Behavior and Aggression in Peromyscus and Their Associations with Vasopressin Immunoreactivity and Receptors

Bester‐Meredith, J. K., Young, L. J., & Marler, C. A. (1999) · Hormones and Behavior · doi:10.1006/hbeh.1999.1522 · Cited by 285

Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP

Klesert, T. R., Otten, A. D., Bird, T. D., & Tapscott, S. J. (1997) · Nature Genetics · doi:10.1038/ng0897-402 · Cited by 265

Neuroendocrine bases of monogamy

Young, L. J., Wang, Z., & Insel, T. R. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01167-3 · Cited by 265

Vasopressin receptor blockade in the anterior hypothalamus suppresses aggression in hamsters

Ferris, C. F., & Potegal, M. (1988) · Physiology & Behavior · doi:10.1016/0031-9384(88)90144-8 · Cited by 259

Amours et neurologie

Collongues, N., Cretin, B., Seze, J. D., & Blanc, F. (2010) · Revue Neurologique · doi:10.1016/j.neurol.2010.03.023 · Cited by 2

Molecular Genetics of Brain Noradrenergic Neurotransmission

Meloni, R. (2008) · Springer eBooks · doi:10.1007/978-0-387-30382-6_6 · Cited by 1

Sexual Motivation in Mateships and Sexual Conflict

Klusmann, D., & Berner, W. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195396706.013.0014 · Cited by 1

Duality of stochasticity and natural selection shape the ecology-driven pattern of social interactions: the fall of Hamilton's rule

Heininger, K. (2015) · doi:10.13140/rg.2.2.26412.95368 · Cited by 1

Neuropeptide Systems and Social Behavior: Noncoding Repeats as a Genetic Mechanism for Rapid Evolution of Social Behavior

Hammock, E. A. D., & Young, L. J. (2007) · Elsevier eBooks · doi:10.1016/b0-12-370878-8/00091-4 · Cited by 1

The evolutionary origins of cooperation and trade

Zak, P. J. (2017) · Journal of Bioeconomics · doi:10.1007/s10818-017-9259-6 · Cited by 1

The neurohypophysis

Ball, S. G. (2011) · doi:10.1093/med/9780199235292.003.2018 · Cited by 1

Unraveling the Neural Basis of Behavioral Isolation through the Lens of Audition in Anurans

Anderson, C. B. (2024) · Brain Behavior and Evolution · doi:10.1159/000542575 · Cited by 1

The effects of prior social experience on reproductive behavior, spawning, and physiology in a monogamous fish, Amatitlania nigrofasciata

Little, K. P. (2014) · Cited by 1

Effects of social experience on pair bonding in a monogamous fish (Amatitlania nigrofasciata)

Little, K. P., Al‐Shaer, L., & Itzkowitz, M. (2017) · Behaviour · doi:10.1163/1568539x-00003436 · Cited by 1

Neurogenetics of Motivation for Physical Activity

Rhodes, J. S. (2019) · Routledge eBooks · doi:10.4324/9781315146287-11 · Cited by 1

SCIENTIFIC THOUGHT AND ABSOLUTES

Longo, G. O., & Gauthier, D. (2020) · Angelaki · doi:10.1080/0969725x.2020.1754031 · Cited by 1

Behavioral, Cognitive, and Genetic Factors Underlying Socio-Communicative Development in Bonobos

Skiba, S. A. (2022) · Digital Archive @ GSU · doi:10.57709/23988841 · Cited by 1

An extended epiphenotype for an extended phenotype in Toxoplasma gondii infected feral house mice

Ngo, P., Lignereux, L., O'Handley, R. M., & Vyas, A. (2022) · Functional Ecology · doi:10.1111/1365-2435.14223 · Cited by 1

The Behavioral Genetics of Human Pair Bonding

Walum, H., & Westberg, L. (2011) · Wiley eBooks · doi:10.1002/9781118101803.ch2 · Cited by 1

The effects of avpr1a microsatellite length and population density on indices of social and genetic monogamy in male prairie voles ( Microtus ochrogaster )

Richmond, A. R. (2007) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1

Genetic Variation in Neurotransmitter Receptors Generates Behavioral Diversity

Bendesky, A. (2025) · Digital Commons - RU (Rockefeller University) · doi:10.48496/3y0n-tx90 · Cited by 1

Mechanisms of space use in the wood mouse, Apodemus sylvaticus

Godsall, B. (2015) · Spiral (Imperial College London) · doi:10.25560/25280 · Cited by 1

Nonapeptide receptor expression in relation to mating system and social behavior in Richardson's ground squirrels

Araujo, J. D. C. (2017) · Cited by 1

Essays in Social Status and Finance

Barradale, N. J. (2010) · eScholarship (California Digital Library) · Cited by 1

The Role of the Preoptic Area in Social Interaction in Zebrafish

Kelly, J. R. (2019) · Liverpool John Moores University · doi:10.24377/ljmu.t.00010853 · Cited by 1

Larry J. Young (1967–2024)

Donaldson, Z. R., Hammock, E. A. D., & Lim, M. M. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01637-z · Cited by 1

Więzi międzyosobnicze, miłość, empatia, altruizm: neurobiologiczne korzenie dobra

Godzińska, E. J. (2007) · Cited by 1

Entwicklung und Kontrolle des Verhaltens

Kappeler, P. M. (2011) · Springer-Lehrbuch · doi:10.1007/978-3-642-20653-5_11

A Comparative Analysis of the Neural Basis for Dorsal-Ventral Swimming in the Nudipleura

Lillvis, J. L. (2022) · Digital Archive @ GSU · doi:10.57709/3074014

Interactions between the BDNF (Val66Met) variant and stress as a model of susceptibility to Anorexia Nervosa

Madra, M. (2015) · doi:10.7916/d8sj1jjv

The Biochemistry of Family Commitment and Youth Competence: Lessons from Animal Models

Young, L. J., & Francis, D. D. (2007) · Springer eBooks · doi:10.1007/978-0-387-72721-9_2

Molecular Evolution of Vasopressin and Oxytocin Receptor Genes in Owl Monkeys (aotus Azarai) of Northern Argentina

Babb, P. L. (2012) · ScholarlyCommons (University of Pennsylvania)

Vasopressin Anatomy of the Mouse Brain

Rood, B. D. (2022) · ScholarWorks@UMassAmherst (University of Massachusetts Amherst) · doi:10.7275/1342007

Relationships between neuronal V1aR expression and single-nucleotide polymorphisms in Microtus ochrogaster

Lai, S. (2017) · Texas ScholarWorks (Texas Digital Library) · doi:10.15781/t24q7r55z

Genetic and hormonal influences on affiliative behavior in humans

Walum, H. (2012) · Figshare

Testosterone and vasopressin in men's reproductive behavior

Steiner, E. T. (2020) · Digital Scholarship - UNLV (University of Nevada Reno) · doi:10.34917/2269036 · Cited by 1

Genes and Behavior: Animal Models

Greenspan, R. J. (2001) · Elsevier eBooks · doi:10.1016/b0-08-043076-7/03350-7

Differences in social approach in two inbred strains of mice

Pratte, M., & Jamon, M. (2011) · Neurocomputing · doi:10.1016/j.neucom.2011.12.016

Neural correlates and modulators of social plasticity

Sakata, J. T. (2002) · Texas ScholarWorks (Texas Digital Library)

The Effects of Arginine Vasopressin on Maternal Behavior and Aggression in Peromyscus californicus Mothers

Ng, N. D. (2015)

Role of arginine vasopressin in modulating plasticity in defensive behavior

Shantala, A. H. D. (2014) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/61632

New insights to the brain functions of prolyl oligopeptidase

Peltonen, I. (2012) · Työväentutkimus Vuosikirja

Pain as a Mediator of Empathetic Response in Mus musculus: Identifying Neuroendocrine Substrates and Sex Differences of Social Approach Behavior

Tuttle, A. H. (2008)

Evolution of Neurotransmitter-Related Genes in Primates

Inoue‐Murayama, M., Niimi, Y., ADACHI, S., MITANI, H., Takenaka, O., Ito, S., & Murayama, Y. (2000) · Primate Research · doi:10.2354/psj.16.69

Primate Groups and Their Correlates

Gagneux, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-08-097086-8.82007-3

ROLE OF VASOPRESSIN VIa RECEPTOR IN HYPERTENSION, DIABETES MELLITUS AND PLATELET FUNCTION: GENETIC POLYMORPHISM STUDY

Hasanl, K. N., Shojil, M., Sugimoto, K., & Tsutaya, S. (2007) · Institutional Repositories DataBase (IRDB)

Selection on two behavioral genes : fitness effects of receptor genes for arginine vasopressin 1a and oxytocin in the bank vole Myodes glareolus

Lönn, E. (2017) · Jyväskylä University Digital Archive (University of Jyväskylä)

Pair bonding, the preferred mating tactic of Microtus ochrogaster, induces changes in expression of aggression and social cognition, but not receptor distribution

Blocker, T. D. (2016) · SHAREOK (University of Oklahoma; Oklahoma State University; Central Oklahoma University)

Memória e socialidade: como o reconhecimento individual afeta formação de grupos

Rios, V. P. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2017.tde-06122016-101748

Evolution of Xenopus Vocal Patterns: Retuning a Hindbrain Circuit During Species Divergence

Barkan, C. L. (2017) · doi:10.7916/d8862tqp

Transcriptional Characterization of Neuronal Cell Populations in Prairie Voles

Kelly, C. J. (2018) · CU Scholar (University of Colorado Boulder)

Stress, Corticosterone, and the Social Behavior of the Prairie Vole Microtus Ochrogaster: An Integrative Approach

Blondel, D. V. (2013) · University of Florida Digital Collections (University of Florida)

Establishment of induced pluripotent stem cells from prairie vole-derived fibroblast

Katayama, M., & Fukuda, T. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822228-7.00001-1

Factores sociales y cambios neuroendocrinos asociados con el inicio de la conducta paterna en el gerbo de Mongolia (Meriones unguiculatus)

Bravo, A. L. M. (2020) · doi:10.24275/uami.44558d45t

Bibliographie

Aron, S., & Passera, L. (2009) · Les sociétés animales · doi:10.3917/dbu.aron.2009.01.0303

Behavioral Genetics

Maxson, S. C. (2003) · Handbook of Psychology · doi:10.1002/9780471264385.wei0302

Promoters: Evolution

Gumucio, D. L. (2007) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0005090.pub2

Peer Review #1 of "Brain transcriptome sequencing and assembly of three songbird model systems for the study of social behavior (v0.1)"

(2014) · PeerJ · doi:10.7287/peerj.396v0.1/reviews/1

Promoters: Evolution

Gumucio, D. L. (2006) · Encyclopedia of Life Sciences · doi:10.1038/npg.els.0005090

Peer Review #2 of "Brain transcriptome sequencing and assembly of three songbird model systems for the study of social behavior (v0.1)"

(2014) · PeerJ · doi:10.7287/peerj.396v0.1/reviews/2

Comment, au fil du temps, l’ocytocine est devenue l’hormone de l’attachement

Freund‐Mercier, M. J. (2022) · Biologie Aujourd hui · doi:10.1051/jbio/2022014

The neurogenetic background of parental care

Fazekas, E. A. (2021) · Eötvös Loránd Tudományegyetem · doi:10.15476/elte.2020.149

Biology of Coital Behavior: Looking Through the Lens of Mathematical GenomicsPreprint

Sil, M., Nawn, D., Hassan, S. S., Chakraborty, S., Goswami, A., Basu, P., Roopesh, L., Wu, E., Lundstrom, K. H., & Uversky, V. N. (2023) · doi:10.22541/au.168132735.57848131/v1

Biology of Coital Behavior: Looking Through the Lens of Mathematical GenomicsPreprint

Sil, M., Nawn, D., Hassan, S. S., Chakraborty, S., Goswami, A., Basu, P., Roopesh, L., Wu, E., Lundstrom, K. H., & Uversky, V. N. (2023) · doi:10.22541/au.168140939.97225898/v1

Biology of Coital Behavior: Looking Through the Lens of Mathematical GenomicsPreprint

Sil, M., Nawn, D., Hassan, S. S., Chakraborty, S., Goswami, A., Basu, P., Roopesh, L., Wu, E., Lundstrom, K. H., & Uversky, V. N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.12.536521

Isotocin Influences Parental Care in Male Threespine Stickleback Across Proximate and Evolutionary Time ScalesPreprint

Dan, U., Maciejewski, M. F., Schwaiger, E., & Bell, A. M. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4846666

Oxytocin

Zingg, H. H. (2002) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00242-4

Fos/AP-1 as an Exemplar for the Study of Neuronal Activity-Dependent Gene Regulation

Griffith, E. C., & Greenberg, M. E. (2024) · Springer eBooks · doi:10.1007/978-3-031-68550-7_1 · Cited by 2

Cellular evolution of the hypothalamic preoptic area of behaviorally divergent deer micePreprint

Chen, J., Richardson, P. R., Kirby, C., Eddy, S. R., & Hoekstra, H. E. (2024) · eLife · doi:10.7554/elife.103109.1

Cellular evolution of the hypothalamic preoptic area of behaviorally divergent deer micePreprint

Chen, J., Richardson, P. R., Kirby, C., Eddy, S. R., & Hoekstra, H. E. (2025) · eLife · doi:10.7554/elife.103109.2

Sex Difference in the Effects of Ventral Pallidum Vasopressin 1a Receptor Knockdown on Social Behavior in MicePreprint

Friesen, C. N., Hartswick, D., Selke, A., Vries, G. J. D., & Petrulis, A. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5265287

Exploring social behaviour using Tinbergen’s 4 Questions

Székely, T. (2025) · Biologia Futura · doi:10.1007/s42977-025-00274-2

A highly contiguous genome assembly for the California vole, Microtus californicus, provides insight into phylogenetic relationships and patterns of synteny among voles

Kozak, K. M., Escalona, M., Linn, I. J., Chumchim, N., Fairbairn, C. W., Marimuthu, M. P. A., Nguyen, O., Seligmann, W., Conroy, C. J., Patton, J. L., et al. (2025) · Journal of Heredity · doi:10.1093/jhered/esaf067

Species-specific behavioural responses to peripheral arginine vasopressin in two African striped mice (genus Rhabdomys)

Neves, C. N., Rymer, T. L., Hartman, K.-J., & Pillay, N. (2025) · Behavioural Processes · doi:10.1016/j.beproc.2025.105284

Recapitulating the length polymorphism of RS3, a composite microsatellite implicated in human social behavior, via recombination in Saccharomyces cerevisiaePreprint

Kean, C. E., Radchenko, E. A., Lindenbaum, N. M., Materne, G., & Mirkin, S. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.09.687482

The Neural and Genetic Basis of Romantic Love

Acevedo, B. P., Bartels, A., Sainz‐Ballesteros, A., & Grassi, P. R. (2025) · Springer eBooks · doi:10.1007/978-3-031-94512-0_63

Transgenic Models for Oxytocin and Vasopressin

Young, L. J., & Insel, T. R. (2001) · Humana Press eBooks · doi:10.1007/978-1-59259-102-2_12

Microevolution and Macroevolution in Behavior

Leonard, J. E., & Boake, C. R. B. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-045337-8.00114-5

Primate Families, Structure of

Gagneux, P. (2001) · Elsevier eBooks · doi:10.1016/b0-08-043076-7/03389-1

Transcriptomic profiling reveals neurophysiological gene candidates underlying vocal evolution in African clawed frogsPreprint

Barkan, C. L., Binder, L. A., Davis, B. A., Carbone, L., & Zornik, E. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.24.701475

Etude de l'implication fonctionnelle de la neurogénèse hippocampique dans la pathophysiologie et le traitement de la dépression

Surget, A. (2008) · theses.fr (ABES) · doi:10.70675/65cd9b5fz7735z4180zb8d6z7ae3b7cbefff

Caractérisation d’outils pharmacologiques pour l’étude des récepteurs centraux de la vasopressine

Marir, R. (2013) · theses.fr (ABES) · doi:10.70675/547ee25cz6fbfz417azabc9z92de6a7a2fcc

Etude de la dimérisation et de la dynamique structurale des mGluR par la technologie trFRET : de nouvelles pistes pour de nouveaux médicaments

Doumazane, E. (2011) · theses.fr (ABES) · doi:10.70675/35aad135z0f70z4530zb264za9a154b42494

Circuits neuronaux sous-tendant la régulation émotionnelle par le système ocytocinergique

Goyon, S. (2018) · theses.fr (ABES) · doi:10.70675/c8c9bec0z7b79z4826z862az93b128e1ada6

Social experience affects patterns of vasopressin receptor 1a expression in a way that differs by sex

Friesen, C. N., Selke, A., Vries, G. J. D., & Petrulis, A. (2026) · Hormones and Behavior · doi:10.1016/j.yhbeh.2026.105931

New regulators in oxytocin and vasopressin release : role of the endolysosomal two-pore channels

Martucci, L. L. (2021) · theses.fr (ABES) · doi:10.70675/027d1ae2zd2ebz4677za019ze6ccd94cafe9

A yeast recombination system recapitulates the length polymorphism of a microsatellite implicated in human social behavior

Kean, C. E., Radchenko, E. A., Lindenbaum, N. M., Materne, G., & Mirkin, S. M. (2026) · NAR Molecular Medicine · doi:10.1093/narmme/ugag032

Transcriptomic profiling reveals neurophysiological gene candidates underlying vocal evolution in African clawed frogs

Barkan, C. L., Binder, L. A., Davis, B. A., Carbone, L., & Zornik, E. (2026) · Journal of Neurophysiology · doi:10.1152/jn.00037.2026

From humans to model organisms: Translational insights into sociability and social dysfunction

Canonero, M., Chan, W. K., Hassan, N., Rasul, M., Shiadeh, S. M. J., Westberg, L., Ardalan, M., & Mallard, C. E. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106919

Effects of a secure attachment relationship on right brain development, affect regulation, and infant mental health

Schore, A. N. (2001) · Infant Mental Health Journal · doi:10.1002/1097-0355(200101/04)22:1

The broad autism phenotype: A complementary strategy for molecular genetic studies of autism

(2001) · doi:10.1002/1096-8628(20010108)105:1

Species differences in V₁a receptor gene expression in monogamous and nonmonogamous voles: Behavioral consequences.

Young, L. J., Winslow, J. T., Nilsen, R., & Insel, T. R. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.3.599 · Cited by 196

Facilitation of Affiliation and Pair-Bond Formation by Vasopressin Receptor Gene Transfer into the Ventral Forebrain of a Monogamous Vole

Pitkow, L. J., Sharer, C. A., Ren, X., Insel, T. R., Terwilliger, E. F., & Young, L. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07392.2001 · Cited by 295

The Role of Vasopressin in the Genetic and Neural Regulation of Monogamy

Lim, M. M., Hammock, E. A. D., & Young, L. J. (2004) · Journal of Neuroendocrinology · doi:10.1111/j.0953-8194.2004.01162.x · Cited by 84

Patterns of brain vasopressin receptor distribution associated with social organization in microtine rodents

Insel, T., Wang, Z., & Ferris, C. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-09-05381.1994 · Cited by 454

Extraordinary diversity in vasopressin (V1a) receptor distributions among wild prairie voles (Microtus ochrogaster): Patterns of variation and covariation

Phelps, S. M., & Young, L. J. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10902 · Cited by 116